Prof. ULUÇ YİŞ

Metrics

Publication

588

Publication (WoS)

306

Publication (Scopus)

272

Citation (WoS)

2887

H-Index (WoS)

Citation (Scopus)

3198

H-Index (Scopus)

Citation (Scholar)

4781

H-Index (Scholar)

Citation (TrDizin)

H-Index (TrDizin)

Citation (Sobiad)

204

H-Index (Sobiad)

Citation (Sum Other)

Project

Thesis Advisory

Open Access

UN Sustainable Development Goals

Announcements & Documents

Thesis Documents

Evaluation of autonomic dysfunction in pediatric migraine patients

424552.pdf

The evaluation of the indications, effectiveness and results of lumbar punctures applied in Dokuz Eylul University children's Hospital

549136.pdf

Assessment of follow-up quality and compliance in patients with Duchenne Muscular Dystrophy and Becker Muscular Dystrophy

710449.pdf

Education

2005 - 2008

Post Doctorate of Medicine

Dokuz Eylul University, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Turkey

2000 - 2005

Expertise In Medicine

Dokuz Eylul University, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Turkey

1994 - 2000

Undergraduate

Ege University, Faculty Of Medicine, Tıp Pr., Turkey

Research Areas

Health Sciences

Research Areas Based on Academic Activities

Avesis Research Areas

WoS Research Areas

Scopus Research Areas

Academic Positions

2011 - Present

Professor

Dokuz Eylul University, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü

2011 - Present

Professor

Dokuz Eylul University, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü

2011 - 2016

Associate Professor

Dokuz Eylul University, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü

Managerial Experience

2025 - Present

Türkiye Çocuk Nörolojisi Dernek Başkanı

Dokuz Eylul University, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü

2020 - Present

Head of Department

Dokuz Eylul University, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü

2023 - 2026

Head of Department

Dokuz Eylul University

2020 - 2023

Head of Department

Dokuz Eylul University

2012 - 2013

Head of Department

Dokuz Eylul University

Supervised Theses

2025

Expertise In Medicine

Çocuk Norolojisi Bilim Dalı'na perioperatif öneriler açısından danışılan hastaların değerlendirilmesi

Yiş U. (Advisor)

Ş.ŞENOL(Student)

2020

Expertise In Medicine

Assessment of follow-up quality and compliance in patients with Duchenne Muscular Dystrophy and Becker Muscular Dystrophy

YİŞ U. (Advisor)

İ.BURAK(Student)

2019

Expertise In Medicine

The evaluation of the indications, effectiveness and results of lumbar punctures applied in Dokuz Eylul University children's Hospital

YİŞ U. (Advisor)

H.DİDEM(Student)

2015

Expertise In Medicine

Evaluation of autonomic dysfunction in pediatric migraine patients

YİŞ U. (Advisor)

D.ELİTEZ(Student)

Articles

2026

1. The role of DHH motifs in PRUNE1 gene on ion channels: A new insight into epilepsy pathogenesis

Günaya Ç., Yılmazbilek İ., SOYDEMİR D., SARIKAYA UZAN G., Özsoy Ö., Yeşilmen M. C., et al.

Epilepsy Research , vol.224, 2026 (SCI-Expanded, Scopus)

2026

2. Dual-task performance as a clinical marker of upper limb decline in Duchenne muscular dystrophy

Savas-Kalender D., Kurt-Aydin M., TARSUSLU T., YİŞ U.

CLINICAL REHABILITATION , 2026 (SCI-Expanded, Scopus)

2026

3. Exploring Molecular Pathways Underlying Epilepsy Development in Intellectual Disability

GÜNAY Ç., Binokay L., KARAKÜLAH G., POLAT A. İ., YİŞ U., Hlz Kurul S.

Neuropediatrics , vol.57, no.2, pp.90-99, 2026 (SCI-Expanded, Scopus)

2026

4. Expanded clinical and genetic characterization of autosomal recessive HMGCR-related muscular dystrophy

El-Hayek S., Rad A., Sedighzadeh S., Yesil G., Sabbagh S., Shahrooei M., et al.

JOURNAL OF NEUROMUSCULAR DISEASES , 2026 (SCI-Expanded, Scopus)

2026

5. Bi-Allelic Variants in MICU1 Cause Myopathy With Extrapyramidal Signs: Case Series, Phenotypic Spectrum, and Genotype–Phenotype Correlations From 61 Patients

Beheshti P., Akbarian F., Esmaeilzadeh E., Galehdari H., Khorrami M., Vallian S., et al.

Clinical Genetics , vol.109, no.3, pp.564-570, 2026 (SCI-Expanded, Scopus)

2026

6. Compliance of comprehensive care in children with Duchenne muscular dystrophy: Real-world experience of a pediatric neuromuscular diseases center

yeyen i. b., GÜNAY Ç., KURUL S. H., YİŞ U.

Developments and experiments in health and medicine , vol.40, no.1, pp.65-75, 2026 (TRDizin)

2026

7. Reliability and discriminative validity of single- and dual-task 10-meter walk test for assessing cognitive-motor interference in children with Duchenne muscular dystrophy

KURT M., Savas-Kalender D., Acarol F. O., TARSUSLU T., YİŞ U.

Physiotherapy Theory and Practice , 2026 (SCI-Expanded, Scopus)

2026

8. Exploring Balance and Functional Mobility in Children with Juvenile Myoclonic Epilepsy, Effects of Cognitive and Motor Dual-Tasks: An Exploratory Pilot Study

Kurt-Aydin M., Savas-Kalender D., Ahmadov R., Tarsuslu T., Gok A., Ulker Ustebay D., et al.

PHYSICAL & OCCUPATIONAL THERAPY IN PEDIATRICS , vol.46, no.2, pp.257-268, 2026 (SCI-Expanded, SSCI, Scopus)

2026

9. Optical genome mapping identifies previously undetected causal variants in early-onset developmental epileptic encephalopathies

Yilmaz S., Avci Durmusalioglu E., Toprak Dogan D. E., Kanmaz S., Atik T., Mutlu M. B., et al.

Journal of Medical Genetics , 2026 (SCI-Expanded, Scopus)

2025

10. Acute Disseminated Encephalomyelitis in Children and Adolescents: A Multicenter Retrospective Study of Relapse and Outcome

Kanmaz S., Yılmaz S., Dündar N. O., Aksoy A., CANPOLAT M., PER H., et al.

Journal of Child Neurology , vol.40, 2025 (SCI-Expanded, Scopus)

2025

11. Navigating pediatric post-stroke epilepsy: comparative assessment of treatment strategies

Günay Ç., HIZ A. S., YİŞ U., AYDIN A., POLAT A. İ.

ACTA NEUROLOGICA BELGICA , vol.125, no.5, pp.1335-1346, 2025 (SCI-Expanded, Scopus)

2025

12. **A Novel HERC2 Variant in Two Siblings with Autosomal Recessive Intellectual Developmental Disorder-38 and Cardiomyopathy**

ŞENOL H. B., Gunay Ç., POLAT A. İ., AYDIN A., HIZ A. S., YİŞ U.

MOLECULAR SYNDROMOLOGY , vol.16, no.5, pp.469-475, 2025 (SCI-Expanded, Scopus)

2025

13. Challenging Mild Hypoxic-Ischemic Encephalopathy: Insights Into Neurological Outcomes

CANBELDEK M., ARMAĞAN C., ŞENOL H. B., BAYKARA H. B., Baykara A. B., Uçar H. G., et al.

TURKISH ARCHIVES OF PEDIATRICS , vol.60, no.5, 2025 (ESCI, Scopus, TRDizin)

2025

14. Evaluation of clinical features of patients diagnosed with spinal muscular atrophy type 1 receiving nusinersen treatment before and after newborn screening program: a multicenter experience in Turkiye

Komur M., Caglar E., Ceylan A., TÜRKDOĞAN D., Herguner O., YILDIZ E., et al.

NEUROMUSCULAR DISORDERS , vol.53, 2025 (SCI-Expanded, Scopus)

2025

15. National plan of action to raise awareness and improve medical care of Duchenne muscular dystrophy (AIM-DMD): first year results

Akinci G., ÖNTAŞ E., Coskun A., Cakir T., Ayanoglu C., Koken O. Y., et al.

NEUROMUSCULAR DISORDERS , vol.53, 2025 (SCI-Expanded, Scopus)

2025

16. Pontocerebellar Hypoplasia and Periventricular Leukomalacia Associated With p.Phe262Val Homozygous Variant in TTC1 Gene: A Report of 4 Cases

SARIKAYA UZAN G., Yaramış A. H., Sönmezler E., HIZ A. S., Yaramış A., YİŞ U., et al.

International Journal of Developmental Neuroscience , vol.85, no.5, 2025 (SCI-Expanded, Scopus)

2025

17. Genetic and clinical spectrum of PIEZO2-related disorders: insights from a multicenter study of 26 patients

Akinci G., Ozyilmaz B., ÖZTÜRK G., Komur M., Onel E., Ardicli D., et al.

Neuromuscular Disorders , vol.53, 2025 (SCI-Expanded, Scopus)

2025

18. Mitochondrial DNA disorders in neuromuscular diseases in diverse populations

Gao F., Schon K. R., Vandrovcova J., Köken Ö. Y., Raga S., Naidu K., et al.

Annals of Clinical and Translational Neurology , vol.12, no.8, pp.1680-1688, 2025 (SCI-Expanded, Scopus)

2025

19. Single sural nerve response: A reliable and practical method for diagnosis of diabetic peripheral neuropathy in children with type 1 diabetes.

Şenol H. B., Şalbaş Ö., Kadem E. N., Halk M., Polat A. İ., Aydın A., et al.

Journal of diabetes investigation , vol.16, no.6, pp.1050-1054, 2025 (SCI-Expanded, Scopus)

2025

20. Phenotypic variability in cases with CACNA1A mutation

Bozkaya-Yilmaz S., Olgac-Dundar N., Aliyeva N., Ersen A., Gencpinar P., Gungor M., et al.

European Journal of Pediatrics , vol.184, no.4, 2025 (SCI-Expanded, Scopus)

2025

21. Nusinersen for children with type I spinal muscular atrophy: 4 years' clinical experience in Turkish cohort

BEKTAŞ Ö., Gulsen M., Dursun O. B., Tekin A., Yuksel D., DEMİR E., et al.

FRONTIERS IN NEUROLOGY , vol.16, 2025 (SCI-Expanded, Scopus)

2025

22. Utility of Optical Genome Mapping in Repeat Disorders

Mutlu M. B., Karakaya T., Çelebi H. B. G., Duymuş F., Seyhan S., Yılmaz S., et al.

Clinical Genetics , vol.107, no.2, pp.188-195, 2025 (SCI-Expanded, Scopus)

2025

23. A Novel PNPLA2 Variant in a Female Patient with Neutral Lipid Storage Disease with Myopathy and Hypogonadotropic Hypogonadism

Şenol H. B., Klsa P., Kulu B., Ören H., Arslan N., Yiş U.

Molecular Syndromology , vol.16, no.1, pp.93-98, 2025 (SCI-Expanded, Scopus)

2025

24. An Unusual Presentation of Leber Hereditary Optic Neuropathy-Plus Case Caused by a Novel DNAJC30 Variant.

Şenol H. B., Soydemir D., Polat A. İ., Aydın A., Hız A. S., Yiş U.

American journal of medical genetics. Part A , vol.197, no.2, 2025 (SCI-Expanded, Scopus)

2025

25. A Novel Splice Site Variant in KLHL40 Gene in Multiple Affected NEM8 Family Members Who Present Phenotypic Variability

Sönmeza B., KOCABEY M., POLAT A. İ., GÜRSOY S., Karaoǧlu P., Horvath R., et al.

Molecular Syndromology , vol.16, no.1, pp.61-68, 2025 (SCI-Expanded, Scopus)

2025

26. Safety and Efficacy of Nusinersen Focusing on Renal and Hematological Parameters in Spinal Muscular Atrophy

Şenol H. B., Yıldız G., Polat A. İ., Aydın A., Hız A. S., Soylu A., et al.

Brain and Behavior , vol.15, no.1, 2025 (SCI-Expanded, Scopus)

2025

27. A web-based survey about pediatric stroke: Knowledge of pediatricians in Turkey

GÜNAY Ç., SARIKAYA UZAN G., HIZ A. S., Polat Kalafatçılar A. İ., YİŞ U.

Pediatrics International , vol.67, no.1, 2025 (SCI-Expanded, Scopus)

2025

28. Exploring Neuropathy and Myopathy in Mitochondrial Diseases: Insights from Nerve Conduction Studies and Electromyography

ŞENOL H. B., BİLEN M., Gunay C., TEKE KISA P., POLAT A. İ., AYDIN A., et al.

JOURNAL OF BEHCET UZ CHILDRENS HOSPITAL , vol.15, no.3, pp.208-216, 2025 (ESCI, TRDizin)

2025

29. MCT8 deficiency: Point of a neurological view

ERDOĞAN I., OLGAÇ DÜNDAR N., GENÇPINAR P., BOZKAYA YILMAZ S., GÜZİN Y., YİŞ U., et al.

Annals of Pediatrics and Neonatal Care , 2025 (Peer-Reviewed Journal)

2025

30. **Symptomatic and Prophylactic Dantrolene Treatment in a Case of RYR1-Related Congenital Myopathy**

Şenol H. B., Polat A. İ., Aydın A., Hız A. S., Yiş U.

ANNALS OF INDIAN ACADEMY OF NEUROLOGY , vol.28, no.1, pp.126-128, 2025 (SCI-Expanded, Scopus)

2024

31. Therapeutic implications of etiology-specific diagnosis of early-onset developmental and epileptic encephalopathies (EO-DEEs): A nationwide Turkish cohort study

Kanmaz S., Tekgul H., Kayilioglu H., Atas Y., Kart P. O., Yildiz N., et al.

Seizure , vol.123, pp.17-25, 2024 (SCI-Expanded, Scopus)

2024

32. Symptomatic and Prophylactic Dantrolene Treatment in a Case of RYR1‑Related Congenital Myopathy

ŞENOL H., POLAT A. İ., AYDIN A., HIZ A. S., YİŞ U.

ANNALS OF INDIAN ACADEMY OF NEUROLOGY , 2024 (SCI-Expanded, Scopus)

2024

33. Evaluation of the Patients with the Diagnosis of Pontocerebellar Hypoplasia: A Multicenter National Study

Cavusoglu D., Ozturk G., Turkdogan D., Kurul S. H., Yis U., Komur M., et al.

CEREBELLUM , vol.23, no.5, pp.1950-1965, 2024 (SCI-Expanded, Scopus)

2024

34. Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes

Berkovic S. F., Neale B. M., Zsurka G., Zizovic M., Zimprich F., Zara F., et al.

Nature Neuroscience , vol.27, no.10, pp.1864-1879, 2024 (SCI-Expanded, Scopus)

2024

35. Evaluation of Autonomic Dysfunction in Pediatric Migraine Patients

AYKOL D., DEMİR N., POLAT A. İ., ÖZTURA İ., YİŞ U., HIZ A. S.

Journal of Behçet Uz children's hospital (Online) , vol.14, no.2, pp.81-90, 2024 (ESCI, TRDizin)

2024

36. COL12A1 Gene Variant and a Review of the Literature: A Case Report of Ullrich Congenital Muscular Dystrophy

İpek R., Çavdartepe B. E., Bozdoğan S. T., YİŞ U.

Molecular Syndromology , vol.15, no.4, pp.311-316, 2024 (SCI-Expanded, Scopus)

2024

37. Investigation of genotype-phenotype and familial features of Turkish dystrophinopathy patients.

Ozkalayci H., Bora E., Cankaya T., Kocabey M., Zubari N. C., Yis U., et al.

Neurogenetics , vol.25, no.3, pp.201-213, 2024 (SCI-Expanded, Scopus)

2024

38. Feasibility of virtual reality and comparison of its effectiveness to biofeedback in children with Duchenne and Becker muscular dystrophies.

Kurt-Aydin M., Savaş-Kalender D., Tarsuslu T., Yis U.

Muscle & nerve , vol.70, pp.82-93, 2024 (SCI-Expanded, Scopus)

2024

39. Effects of Hemogram Parameters on Remission Durations in Self-Limited Epilepsy with Centrotemporal Spikes

GÜNAY Ç., Sarikaya Uzan G., ÖZSOY Ö., HIZ A. S., YİŞ U.

JOURNAL OF PEDIATRIC NEUROLOGY , vol.22, 2024 (ESCI, Scopus)

2024

40. Alternative splicing expands the clinical spectrum of NDUFS6-related mitochondrial disorders.

Armirola-Ricaurte C., Zonnekein N., Koutsis G., Amor-Barris S., Pelayo-Negro A. L., Atkinson D., et al.

Genetics in medicine : official journal of the American College of Medical Genetics , vol.26, no.6, pp.101117, 2024 (SCI-Expanded, Scopus)

2024

41. Periferik Sinir Hastalıkları: Herediter Nöropatiler

Yiş U., Paketçi C.

Türkiye Klinikleri Pediatri Dergisi , pp.37-41, 2024 (TRDizin)

2024

42. Single-center Experience of Therapeutic Plasma Exchange in Children with Neuroimmunological Disorders: Indications, Efficacy, and Safety

YİŞ U., GÜNAY Ç., ARSLAN G., ÖZSOY Ö., SARIKAYA UZAN G., AYKOL D., et al.

İzmir Tepecik Eğitim Hastanesi Dergisi , 2024 (TRDizin)

2024

43. Anaemia-based screening for resistance to thyroid hormone alpha in children

Kağızmanlı G., Kırbıyık Ö., Abacı A., Böber E., Yiş U., Demir K.

CLINICAL ENDOCRINOLOGY , vol.100, no.3, pp.304-311, 2024 (SCI-Expanded, Scopus)

2024

44. Dual task impact on functional mobility and interaction of functional level and balance in patients with Duchenne muscular dystrophy.

Savas-Kalender D., Kurt-Aydin M., Acarol F. O., Tarsuslu T., Yis U.

Gait & posture , vol.108, pp.282-288, 2024 (SCI-Expanded, Scopus)

2024

45. Optic neuritis in Turkish children and adolescents: A multicenter retrospective study.

Direk M. Ç., Besen Ş., Öncel İ., Günbey C., Özdoğan O., Orgun L. T., et al.

Multiple sclerosis and related disorders , vol.81, pp.105149, 2024 (SCI-Expanded, Scopus)

2023

46. Pediatric Pseudotumor Cerebri Syndrome Secondary to Superior Sagittal Sinus Thrombosis Associated with Severe Acute Respiratory Syndrome Coronavirus 2 Infection and Brief Literature Review

YEŞİLMEN M. C., GÜNAY Ç., SARIKAYA UZAN G., ÖZSOY Ö., HIZ A. S., YAŞAR E., et al.

Journal of Behçet Uz children's hospital (Online) , vol.13, pp.203-206, 2023 (ESCI, TRDizin)

2023

47. Phenotypic comparison of a novel variant (p.P164R) and A founder mutation (c.748+1G>A) in Warburg Micro syndrome

Cinleti T., Sarıkaya Uzan G., Bürçe B., Küçümen Y., Yalçın H. Y., Gürsoy S., et al.

NEUROLOGY ASIA , vol.28, no.4, pp.1085-1094, 2023 (SCI-Expanded, Scopus)

2023

48. Clinical and genetic evaluations of rare childhood epilepsies in Turkey's national cohort

Ünalp A., Güzin Y., Ünay B., Tosun A., Çavuşoğlu D., Tekin H. G., et al.

Epileptic Disorders , vol.25, no.6, pp.924, 2023 (SCI-Expanded, Scopus)

2023

49. Phenotypic comparison of a novel variant (p.P164R) and A founder mutation (c.748+1G>A) in Warburg Micro syndrome

Cinleti T., Sarıkaya Uzan G., Bürçe B., Küçümen Y., Yalçın H. Y., Gürsoy S., et al.

NEUROLOGY ASIA , vol.28, no.4, pp.1085-1094, 2023 (SCI-Expanded, Scopus)

2023

50. Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Montanucci L., Collins R. L., Niestroj L., Parthasarathy S., Xian J., Ganesan S., et al.

Nature Communications , vol.14, no.1, 2023 (SCI-Expanded, Scopus)

2023

51. Genetic, serological and clinical evaluation of childhood myasthenia syndromes- single center subgroup analysis experience in Turkey

Özsoy Ö., Cinleti T., Günay Ç., Sarıkaya Uzan G., Giray Bozkaya Ö., Çağlayan A. O., et al.

ACTA NEUROLOGICA BELGICA , vol.123, no.6, pp.2325-2335, 2023 (SCI-Expanded, Scopus)

2023

52. Importance of Vitamin D Status and Nerve Conduction in Pediatric Cystic Fibrosis Patients

Polat I., Kose S. S., AYANOĞLU M., Okur D., BAYRAM E., YİŞ U., et al.

JOURNAL OF PEDIATRIC NEUROLOGY , vol.21, 2023 (ESCI, Scopus)

2023

53. Neuromuscular disease genetics in underrepresented populations: increasing data diversity.

Wilson L. A., Macken W. L., Perry L. D., Record C. J., Schon K. R., Frezatti R. S. S., et al.

Brain : a journal of neurology , vol.146, pp.5098-5109, 2023 (SCI-Expanded, Scopus)

2023

54. Vitamin B12 Deficiency in Pediatric Neurology Practice

GÜNAY Ç., SARIKAYA UZAN G., ÖZSOY Ö., HIZ A. S., YİŞ U.

Haydarpaşa Numune Medical Journal , vol.63, pp.377-383, 2023 (TRDizin)

2023

55. The COVID-19 pandemic restrictions affect the healthcare and health status of paediatric patients with neuromuscular diseases: a developing country perspective

Kurt M., Savas D., TARSUSLU T., YİŞ U.

SOMATOSENSORY AND MOTOR RESEARCH , vol.40, 2023 (SCI-Expanded)

2023

56. Molecular Diagnosis of Limb-Girdle Muscular Dystrophy Using Next-Generation Sequencing Panels

Sarıkaya Uzan G., Yılmaz Uzman C., Çinleti T., Günay Ç., Ülgenalp A., Hız A. S., et al.

MOLECULAR SYNDROMOLOGY , vol.1, pp.1-8, 2023 (SCI-Expanded, Scopus)

2023

57. Evaluation of risk factors for recurrence of cutaneous adverse reactions due to anti-seizure medications in children: A retrospective study

GÜNAY Ç., Uzan G. S., ASİLSOY S., UZUNER N., Kangallı Ö., HIZ A. S., et al.

Current Journal of Neurology , vol.22, no.4, pp.210-216, 2023 (ESCI, Scopus)

2023

58. Role of serostatus in pediatric neuromyelitis optica spectrum disorders: A nationwide multicentric study

Solmaz I., ÖNCEL İ. H., Konuşkan B., Erol I., Orgun L. T., Yılmaz Ü., et al.

Multiple Sclerosis and Related Disorders , vol.77, 2023 (SCI-Expanded, Scopus)

2023

59. Expanding the genotypic and phenotypic spectrum of the SPTBN4 gene mutation: A new variant and dysmorphology

Günay Ç., Onay H., Bademkıran F., Hız A. S., Yiş U.

NEUROLOGY ASIA , vol.28, pp.775-779, 2023 (SCI-Expanded, Scopus)

2023

60. Evaluation of vincristine-induced peripheral neuropathy in children with cancer: Turkish validity and reliability study

Özdemir B., ÖZALP GERÇEKER G., ÖZDEMİR E. Z., Yildirim B. G., ÖREN H., YİŞ U., et al.

Journal of Pediatric Nursing , vol.72, pp.185-190, 2023 (SCI-Expanded, SSCI, Scopus)

2023

61. Anemia-based Screening for Resistance to Thyroid Hormone Alpha in Children

Kagizmanli G., Kirbiyik O., ABACI A., BÖBER E., YİŞ U., DEMİR K.

HORMONE RESEARCH IN PAEDIATRICS , vol.96, pp.428, 2023 (SCI-Expanded, Scopus)

2023

62. DPAGT1-CDG: Report of Two New Pediatric Patients and Brief Review of the Literature

ÖZSOY Ö., ÇİNLETİ T., GÜNAY Ç., SARIKAYA UZAN G., YEŞİLMEN M. C., Lochmueller H., et al.

MOLECULAR SYNDROMOLOGY , vol.14, pp.322-330, 2023 (SCI-Expanded, Scopus)

2023

63. Double Trouble: A Case of DYT-TOR1A Diagnosed in the Postoperative Period

Sarıkaya Uzan G., Günay Ç., Hız A. S., Yiş U.

ANNALS OF INDIAN ACADEMY OF NEUROLOGY , vol.26, no.4, pp.578-580, 2023 (SCI-Expanded, Scopus)

2023

64. Pediatric-Onset Chronic Inflammatory Demyelinating Polyneuropathy: A Multicenter Study

SARIKAYA UZAN G., Vural A., Yüksel D., Aksoy E., Öztoprak Ü., CANPOLAT M., et al.

Pediatric Neurology , vol.145, pp.3-10, 2023 (SCI-Expanded, Scopus)

2023

65. The fate of spikes in self-limited epilepsy with centrotemporal spikes: Are clinical and baseline EEG features effective?

Günay Ç., Sarikaya Uzan G., Özsoy Ö., Hiz Kurul S., Yiş U.

EPILEPSY RESEARCH , vol.193, 2023 (SCI-Expanded, Scopus)

2023

66. Immunization status of patients with spinal muscular atrophy receiving nusinersen therapy

YEŞİLMEN M. C., GÜNAY Ç., Sarıkaya Uzan G., ÖZSOY Ö., HIZ A. S., YİŞ U.

Archives de Pediatrie , vol.30, no.5, pp.291-296, 2023 (SCI-Expanded, Scopus)

2023

67. A novel DOCK7 variant as a rare reason for epileptic encephalopathy, cortical blindness, dysmorphic features: A case report and brief review of the literature

Özsoy Ö., ÇİNLETİ T., Zeybek S., Soydemir D., Uzan G. S., Günay Ç., et al.

NEUROLOGY ASIA , vol.28, no.2, pp.421-429, 2023 (SCI-Expanded, Scopus)

2023

68. A novel DOCK7 variant as a rare reason for epileptic encephalopathy, cortical blindness, dysmorphic features: A case report and brief review of the literature

Özsoy Ö., Cinleti T., Zeybek S., Soydemir D., Sarıkaya Uzan G., Günay Ç., et al.

NEUROLOGY ASIA , vol.28, pp.421-429, 2023 (SCI-Expanded, Scopus)

2023

69. The psychometric properties of Turkish version of the Modified Paediatric Mini Mental Scale

Kurt M., Savaş D., Tarsuslu Şimşek T., Yiş U.

CHILD CARE HEALTH AND DEVELOPMENT , vol.49, no.3, pp.572-578, 2023 (SCI-Expanded, SSCI, Scopus)

2023

70. Bilateral Sensorineural Hearing Loss in AKT3 Mutation: A Case Report and Brief Review of the Literature.

Günay Ç., Kurul S. H., Yiş U.

Annals of Indian Academy of Neurology , vol.26, no.3, pp.293-296, 2023 (SCI-Expanded, Scopus)

2023

71. Examination of the psychometric properties of pediatric-modified total neuropathy score in Turkish children with cancer.

Özdemir B., Gerçeker G., Özdemir E. Z., Yıldırım B. G., Ören H., Yiş U., et al.

Journal of pediatric nursing , vol.69, pp.31-37, 2023 (SCI-Expanded, SSCI, Scopus)

2023

72. What is the safe observation period for seizure recurrence in pediatric emergency departments?

Ulusoy E., Uysal Ateş Ş., Çitlenbik H., Öztürk A., Şık N., Arslan G., et al.

Epilepsy & behavior : E&B , vol.139, pp.109049, 2023 (SCI-Expanded, Scopus)

2023

73. Sural Sparing Pattern and Sensory Ratio as Electrodiagnostic and Prognostic Markers in Pediatric Guillain-Barre Syndrome

Günay Ç., Sarikaya Uzan G., Hiz-Kurul S., Yiş U.

NEUROPEDIATRICS , vol.54, no.1, pp.20-30, 2023 (SCI-Expanded, Scopus)

2023

74. Vitamin B12 Deficiency in Pediatric Neurology Practise

Günay Ç., Sarıkaya Uzan G., Özsoy Ö., Hız A. S., Yiş U.

Haydarpaşa Numune Medical Journal , vol.64, no.3, pp.377-383, 2023 (TRDizin)

2023

75. Factors associated with balance ability in Duchenne and Becker muscular dystrophies

Kurt M., Savas D., TARSUSLU T., Yis U.

GAIT & POSTURE , vol.99, pp.139-145, 2023 (SCI-Expanded, Scopus)

2022

76. Shared Biological Pathways and Processes in Patients with Intellectual Disability: A Multicenter Study

Günay Ç., Aykol D., Özsoy Ö., Sönmezler E., Hancı Y. S., Kara B., et al.

Neuropediatrics , vol.54, no.4, pp.225-238, 2022 (SCI-Expanded, Scopus)

2022

77. Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes

Yiş U.

EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.41, pp.8-18, 2022 (SCI-Expanded, Scopus)

2022

78. Stimulated biofeedback training for a child with Becker muscular dystrophy and compartment syndrome in the left forearm

KURT M., Savas D., TARSUSLU ŞİMŞEK T., YİŞ U.

PHYSIOTHERAPY THEORY AND PRACTICE , vol.38, no.11, pp.1807-1812, 2022 (SCI-Expanded, Scopus)

2022

79. The Effect of Nusinersen Therapy on Laboratory Parameters of Patients with Spinal Muscular Atrophy

Sarıkaya Uzan G., Paketçi C., Günay Ç., Edem P., Özsoy Ö., Hız A. S., et al.

NEUROPEDIATRICS , vol.53, no.5, pp.321-329, 2022 (SCI-Expanded, Scopus)

2022

80. Otizm Spektrum Bozukluğunda Elektroensefalografinin Rolü: Çocuk Nörolojisi Bakışı

Sarıkaya Uzan G., Günay Ç., Özsoy Ö., Hız A. S., Yiş U.

Dokuz Eylül Üniversitesi Tıp Fakültesi Dergisi , vol.36, no.22, pp.123-133, 2022 (TRDizin)

2022

81. Epilepsy and Electroencephalographic Abnormalities in Children with Autistic Spectrum Disorder

Polat I., HIZ A. S., YİŞ U., Ayanoglu M., Okur D., BAYRAM E., et al.

JOURNAL OF DR BEHCET UZ CHILDRENS HOSPITAL , vol.12, no.2, pp.107-115, 2022 (ESCI, TRDizin)

2022

82. Blood neurofilament light chain and thrombospondin-1 levels of patients with autism spectrum disorder.

Paketçi C., Ermiş Ç., Şişman A., Hız S., Baykara B., Yiş U.

Turkish journal of medical sciences , vol.52, no.4, pp.1041-1049, 2022 (SCI-Expanded, Scopus, TRDizin)

2022

83. Optic neuritis in CD59 deficiency: an extremely rare presentation

Gunay C., Yardim E., Yasar E., HIZ A. S., Uzan G. S., Ozturk T., et al.

TURKISH JOURNAL OF PEDIATRICS , vol.64, no.4, pp.787-794, 2022 (SCI-Expanded, Scopus, TRDizin)

2022

84. The impacts of poor glycemic control and disease duration on peripheral nerves in children and adolescents with type 1 diabetes mellitus

AYANOĞLU M., YİŞ U., ÜNVER TUHAN H., POLAT A. İ., OKUR T. D., EDEM P., et al.

NEUROLOGY ASIA , vol.27, no.2, pp.317-326, 2022 (SCI-Expanded, Scopus)

2022

85. Red ear syndrome: Three new pediatric cases

Gunay C., HIZ A. S., Erdag T. K., OLGUN Y., YİŞ U.

NEUROLOGY ASIA , vol.27, no.2, pp.521-525, 2022 (SCI-Expanded, Scopus)

2022

86. Neuromuscular diseases in the pediatric intensive care unit: 11 years of experience from a tertiary children's hospital

Sarikaya Uzan G., Edem P., Besci T., Paketci C., Evren G., HIZ A. S., et al.

NEUROLOGY ASIA , vol.27, no.2, pp.327-334, 2022 (SCI-Expanded, Scopus)

2022

87. Recurrent painful ophthalmoplegic neuropathy: a report of two new pediatric cases

Gunay C., Edem P., HIZ A. S., Yasar E., YİŞ U.

TURKISH JOURNAL OF PEDIATRICS , vol.64, no.3, pp.592-598, 2022 (SCI-Expanded, Scopus, TRDizin)

2022

88. High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases

HIZ A. S., OKTAY Y., Topf A., Szabo N. Z., GÜNGÖR S., Yaramis A., et al.

BRAIN , vol.145, no.4, pp.1507-1518, 2022 (SCI-Expanded, Scopus)

2022

89. Heterogeneity of PNPT1 neuroimaging: Mitochondriopathy, interferonopathy or both?

Pennisi A., Rötig A., Roux C., Lévy R., Henneke M., Gärtner J., et al.

Journal of Medical Genetics , vol.59, no.2, pp.204-208, 2022 (SCI-Expanded, Scopus)

2022

90. Biallelic Loss-of-Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh-Like Syndrome to Isolated Optic Atrophy

Magrinelli F., Cali E., Braga V. L., YİŞ U., Tomoum H., Shamseldin H., et al.

MOVEMENT DISORDERS CLINICAL PRACTICE , vol.9, pp.218-228, 2022 (SCI-Expanded, ESCI, Scopus)

2022

91. Evaluation of the Genetically Diagnosed Mitochondrial Disease Cases with Neuromuscular Involvement

GÜNAY Ç., Paketci C., Edem P., SARIKAYA UZAN G., HIZ A. S., ARSLAN GÜLTEN Z., et al.

IZMIR DR BEHCET UZ COCUK HASTANESI DERGISI , vol.12, no.1, pp.27-36, 2022 (ESCI, TRDizin)

2022

92. VARS1 mutations associated with neurodevelopmental disorder are located on a short amino acid stretch of the anticodon-binding domain

Hız A. S., Kılıç S., Bademci G., Karakulak T., Erdogan A., Ozden B., et al.

Turkish Journal of Biology , vol.46, no.6, pp.458-464, 2022 (SCI-Expanded, Scopus, TRDizin)

2022

93. Evaluation of the Pediatric Neurology Consultations Requested from the Pediatric Emergency Service: A Single-Center Experience

GÜNAY Ç., PAKETÇİ C., SARIKAYA UZAN G., SOYDEMİR D., KARAKAYA Ö., Elitez D., et al.

JOURNAL OF DR BEHCET UZ CHILDRENS HOSPITAL , vol.12, no.1, pp.81-90, 2022 (ESCI)

2022

94. Evaluation of the Genetically Diagnosed Mitochondrial Disease Cases with Neuromuscular Involvement

GÜNAY Ç., PAKETÇİ C., EDEM P., Sarıkaya Uzun G., HIZ A. S., ARSLAN GÜLTEN Z., et al.

JOURNAL OF DR BEHCET UZ CHILDRENS HOSPITAL , vol.12, no.1, pp.27-36, 2022 (ESCI)

2022

95. Inflammation and endothelial dysfunction in pediatric migraine patients

Polat I., KARAOĞLU P., Sisman A., YİŞ U., HIZ A. S.

PEDIATRICS INTERNATIONAL , vol.64, no.1, 2022 (SCI-Expanded, Scopus)

2021

96. The KCNB1 phenotypic and genetic spectrum

Reale C., Fenger C. D., Neu A., Sukno S., McKeown S., Borovikov A., et al.

EPILEPSIA , vol.62, pp.222-223, 2021 (SCI-Expanded, Scopus)

2021

97. Functional analysis of patient-derived cells harboring a homoygous likely-pathogenic KATNAL2 variant

HIZ A. S., Sonmezler E., YİŞ U., Oktay Y.

EPILEPSIA , vol.62, pp.227-228, 2021 (SCI-Expanded, Scopus)

2021

98. Distinct gene-set burden patterns underlie common generalized and focal epilepsies

Yiş U.

EBIOMEDICINE , vol.72, pp.1-13, 2021 (SCI-Expanded, Scopus)

2021

99. Carbamazepine-Induced Nonepileptic Myoclonus in a Child with Autism and Epilepsy

Kirik S., YİŞ U.

JOURNAL OF PEDIATRIC EPILEPSY , vol.10, no.03, pp.121-123, 2021 (ESCI)

2021

100. Antiviral microRNA expression signatures are altered in subacute sclerosing panencephalitis

Tufekci K. U., Allmer J., Carman K. B., BAYRAM E., TOPÇU Y., Hiz S., et al.

NEUROLOGICAL SCIENCES AND NEUROPHYSIOLOGY , vol.38, no.3, pp.166-172, 2021 (SCI-Expanded, Scopus, TRDizin)

2021

101. The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice

Vural A., Simsir G., Tekgul S., Kocoglu C., Akcimen F., Kartal E., et al.

MOVEMENT DISORDERS , vol.36, no.7, pp.1676-1688, 2021 (SCI-Expanded, Scopus)

2021

102. Clinical and genetic characterization of PYROXD1-related myopathy patients from Turkey

Daimagueler H., Akpulat U., Oezdemir O., YİŞ U., GÜNGÖR S., TALİM B., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.185, no.6, pp.1678-1690, 2021 (SCI-Expanded, Scopus)

2021

103. Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

Motelow J. E., Povysil G., Dhindsa R. S., Stanley K. E., Allen A. S., Feng Y. A., et al.

AMERICAN JOURNAL OF HUMAN GENETICS , vol.108, no.6, pp.965-982, 2021 (SCI-Expanded, Scopus)

2021

104. Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease

Keller N., Paketci C., Altmueller J., Fuhrmann N., Wunderlich G., Schrank B., et al.

HUMAN MUTATION , vol.42, no.4, pp.460-472, 2021 (SCI-Expanded, Scopus)

2021

105. Çocuk yoğun bakım ünitesinde izlenen olguların elektroensefalografi sonuçlarının geriye dönük olarak değerlendirilmesi. The evaluation of electroencephalogram results in patients hospitalized in the pediatric intensive care unit

AYANOĞLU M., YİŞ U., POLAT A. İ., KÖKER A., ARSLAN G., HIZ A. S.

Pamukkale Tıp Dergisi , vol.14, no.4, pp.804-810, 2021 (Scopus, TRDizin)

2021

106. Asemptomatik SARS‐COV‐2 Pozitif Spinal Müsküler Atrofi Tip 1 Olgusu

Sarıkaya Uzan G., Soydemir D., Günay Ç., Güzel I., Sayıner A. A., Hız A. S., et al.

Dokuz Eylül Üniversitesi Tıp Fakültesi Dergisi , vol.35, no.1, pp.279-283, 2021 (TRDizin)

2021

107. Rare presentation of levamisole-induced leukoencephalopathy in a pediatric patient: seizure

Paketci C., Okur D., Hiz S., YİŞ U.

TURKISH JOURNAL OF PEDIATRICS , vol.63, no.2, pp.319-322, 2021 (SCI-Expanded, Scopus)

2021

108. De novo DNM1L variant presenting with severe muscular atrophy, dystonia and sensory neuropathy

Keller N., Paketci C., Edem P., Thiele H., YİŞ U., Wirth B., et al.

EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.64, no.2, 2021 (SCI-Expanded, Scopus)

2021

109. Clinical predictors of drug-resistant epilepsy in children

Karaoglu P., YİŞ U., Polat A. İ., Ayanoglu M., Hiz S.

TURKISH JOURNAL OF MEDICAL SCIENCES , vol.51, no.3, pp.1249-1252, 2021 (SCI-Expanded, Scopus, TRDizin)

2021

110. **Autosomal recessive variants in TUBGCP2 alter the γ-tubulin ring complex leading to neurodevelopmental disease**

GÜNGÖR S., OKTAY Y., Hiz S., Aranguren-Ibanez A., Kalafatcilar I., Yaramis A., et al.

ISCIENCE , vol.24, no.1, 2021 (SCI-Expanded, Scopus)

2021

111. Pediatrik Guillain Barre Sendromu: Klinik, Elektrofizyolojik ve Prognostik Özellikler

Paketçi C., Edem P., Soydemir D., Sarıkaya Uzan G., Günay Ç., Hız A. S., et al.

Dokuz Eylül Üniversitesi Tıp Fakültesi Dergisi , vol.34, no.3, pp.193-202, 2021 (TRDizin)

2021

112. Inflammation and anemia in simple febrile seizures and complex febrile seizures

POLAT A. İ., KARAOĞLU P., AYANOĞLU M., ÇIRALI C., BAYRAM E., YİŞ U., et al.

Annals of Medical Research , vol.28, no.10, pp.1835-1839, 2021 (TRDizin)

2021

113. Could polyneutritis cranialis-related SARS-CoV-2 be a precursor of multi-systemic involvement?

Gök A., Ülker Üstebay D. Ü., İnce D., Hız A. S., Yiş U.

Dokuz Eylül Üniversitesi Tıp Fakültesi Dergisi , vol.35, no.50, pp.273-278, 2021 (TRDizin)

2021

114. Acute flaccid myelitis outbreak through 2016-2018: A multicenter experience from Turkey

ÜNVER O., TÜRKDOĞAN D., Guler S., Kipoglu O., GÜNGÖR M., Paketci C., et al.

EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.30, pp.113-120, 2021 (SCI-Expanded, Scopus)

2021

115. Risk Factors of Post-Stroke Epilepsy in Children; Experience from a Tertiary Center and a Brief Review of the Literature

Polat I., YİŞ U., Ayanoglu M., Okur D., Edem P., Paketci C., et al.

JOURNAL OF STROKE & CEREBROVASCULAR DISEASES , vol.30, no.1, 2021 (SCI-Expanded, Scopus)

2020

116. A homozygous missense variant inTUBGCP2alter the g-tubulin ring complex leading to abnormal cortical development, pontocerebellar atrophy and altered myelination

Oktay Y., Gungor S., Hiz S., Yaramis A., Aranguren-Ibanez A., Yis U., et al.

EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.SUPPL 1, pp.460-461, 2020 (SCI-Expanded, Scopus)

2020

117. Clinical, electrophysiological and genetic characteristics of childhood hereditary polyneuropathies

Paketci C., Karakaya M., Edem P., Bayram E., Keller N., Daimagueler H., et al.

REVUE NEUROLOGIQUE , vol.176, no.10, pp.846-855, 2020 (SCI-Expanded, Scopus)

2020

118. Variants causing mitochondrial dysfunction are not rare in non-5q SMA: Re-evaluation of thirty families by exome sequencing

Karakaya M., Keller N., Altmueller J., Motameny S., Thiele H., Wunderlich G., et al.

EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.SUPPL 1, pp.442, 2020 (SCI-Expanded, Scopus)

2020

119. Improved Diagnosis of Rare Disease Patients through Systematic Detection of Runs of Homozygosity

Yiş U.

JOURNAL OF MOLECULAR DIAGNOSTICS , vol.22, no.9, pp.1205-1215, 2020 (Peer-Reviewed Journal)

2020

120. Neuroprotective Effects of Lacosamide and Memantine on Hyperoxic Brain Injury in Rats

Polat I., CİLAKER MIÇILI S., Calisir M., Bayram E., YİŞ U., Ayanoglu M., et al.

NEUROCHEMICAL RESEARCH , vol.45, no.8, pp.1920-1929, 2020 (SCI-Expanded, Scopus)

2020

121. Successful treatment of intractable epilepsy with ketogenic diet therapy in twins with ALG3-CDG

Paketci C., Edem P., Hiz S., Sonmezler E., Soydemir D., Uzan G., et al.

BRAIN & DEVELOPMENT , vol.42, no.7, pp.539-545, 2020 (SCI-Expanded, Scopus)

2020

122. Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects

Yiş U.

BRAIN : A JOURNAL OF NEUROLOGY , vol.143, pp.2106-2118, 2020 (SCI-Expanded, Scopus)

2020

123. Herpes simplex virus-1 as a rare etiology of isolated acute cerebellitis: case report and literature review

Paketci C., Edem P., Okumus C., Sarioglu F. C., Bayram E., Hiz S., et al.

JOURNAL OF NEUROVIROLOGY , vol.26, no.2, pp.270-272, 2020 (SCI-Expanded, Scopus)

2020

124. Congenital myasthenic syndrome-associated agrin variants affect clustering of acetylcholine receptors in a domain- specific manner

Ohkawara B., Shen X., Selcen D., Nazim M., Bril V., Tarnopolsky M. A., et al.

JCI INSIGHT , vol.5, no.7, 2020 (SCI-Expanded, Scopus)

2020

125. Identification of PCDH19 gene mutations/deletions in patients with early onset epilepsy

Gursoy S., Ataman E., Baysal B. T., Ozyilmaz B., Gencpinar P., HIZ A. S., et al.

ANNALS OF INDIAN ACADEMY OF NEUROLOGY , vol.23, no.2, pp.206-210, 2020 (SCI-Expanded, Scopus)

2020

126. A Drug Reaction With Eosinophilia and Systemic Symptoms Syndrome Associated With Clobazam

Manyas H., Paketci C., Okur D., Bayram E., Hiz S., YİŞ U.

PEDIATRIC EMERGENCY CARE , vol.36, no.3, 2020 (SCI-Expanded, Scopus)

2020

127. Severe neurodevelopmental disease caused by a homozygous TLK2 variant

Topf A., OKTAY Y., Balaraju S., Yilmaz E., Sonmezler E., YİŞ U., et al.

EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.3, pp.383-387, 2020 (SCI-Expanded, Scopus)

2020

128. y COL4A1-related autosomal recessive encephalopathy in 2 Turkish children

Yaramis A., Lochmueller H., Topf A., Sonmezler E., Yilmaz E., Hiz S., et al.

NEUROLOGY-GENETICS , vol.6, no.1, 2020 (SCI-Expanded, Scopus)

2020

129. Intravenous levetiracetam for treatment of seizures in term and preterm neonates

KARAOĞLU P., Hiz S., Iscan B., Polat A. İ., Ayanoglu M., DUMAN N., et al.

JOURNAL OF PEDIATRIC NEUROSCIENCES , vol.15, no.1, pp.15-20, 2020 (ESCI, Scopus)

2020

130. On the differential diagnosis of neuropathy in neurogenetic disorders

Cirak S., Daimaguler H., Moawia A., Koy A., YİŞ U.

MEDIZINISCHE GENETIK , vol.32, no.3, pp.243-261, 2020 (SCI-Expanded, Scopus)

2020

131. Rotavirus encephalopathy with concomitant acute cerebellitis: report of a case and review of the literature

Paketci C., Edem P., Okur D., Sarioglu F. C., GÜLERYÜZ UÇAR H., Bayram E., et al.

TURKISH JOURNAL OF PEDIATRICS , vol.62, no.1, pp.119-124, 2020 (SCI-Expanded, Scopus, TRDizin)

2020

132. Confirmation of TACO1 as a Leigh Syndrome Disease Gene in Two Additional Families

OKTAY Y., GÜNGÖR S., Zeltner L., Wiethoff S., Schoels L., Sonmezler E., et al.

JOURNAL OF NEUROMUSCULAR DISEASES , vol.7, no.3, pp.301-308, 2020 (SCI-Expanded, Scopus)

2019

133. Polygenic burden in focal and generalized epilepsies

Leu C., Stevelink R., Smith A. W., Goleva S. B., Kanai M., Ferguson L., et al.

Brain , vol.142, no.11, pp.3473-3481, 2019 (SCI-Expanded, Scopus)

2019

134. Bi-allelic mutations in PRUNE lead to neurodegeneration with spinal motor neuron involvement and hyperCKaemia

Okur D., Daimaguler H. S., Danyeli A. E., TEKGÜL H., Wang H., Wunderlich G., et al.

TURKISH JOURNAL OF PEDIATRICS , vol.61, no.6, pp.931-936, 2019 (SCI-Expanded, Scopus, TRDizin)

2019

135. Impact of next-generation sequencing panels in the evaluation of limb-girdle muscular dystrophies

Ozyilmaz B., Kirbiyik O., Ozdemir T. R., Ozer O. K., Kutbay Y. B., Erdogan K. M., et al.

ANNALS OF HUMAN GENETICS , vol.83, no.5, pp.331-347, 2019 (SCI-Expanded, Scopus)

2019

136. Biallelic variant in AGTPBP1 causes infantile lower motor neuron degeneration and cerebellar atrophy

Karakaya M., Paketci C., Altmueller J., Thiele H., Hoelker I., YİŞ U., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.179, no.8, pp.1580-1584, 2019 (SCI-Expanded, Scopus)

2019

137. Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

Feng Y. A., Howrigan D. P., Abbott L. E., Tashman K., Cerrato F., Singh T., et al.

AMERICAN JOURNAL OF HUMAN GENETICS , vol.105, no.2, pp.267-282, 2019 (SCI-Expanded, Scopus)

2019

138. Awareness and knowledge levels of osteoporosis in patients with neuromuscular diseases: a multicentre study

Dilek B., Şahin E., Sertpoyraz F. M., Erdinc Gunduz N., Dikici A., Engin O., et al.

NEUROLOGICAL SCIENCES AND NEUROPHYSIOLOGY , vol.36, no.2, pp.120-124, 2019 (SCI-Expanded, Scopus, TRDizin)

2019

139. Giant axonal neuropathy: A differential diagnosis of consideration

Edem P., Karakaya M., Wirth B., Okur T. D., YİŞ U.

TURKISH JOURNAL OF PEDIATRICS , vol.61, no.2, pp.275-278, 2019 (SCI-Expanded, Scopus, TRDizin)

2019

140. Dihydropyridine Receptor Congenital Myopathy In A Consangineous Turkish Family

YİŞ U., Hiz S., Gunes S., Diniz G., Baydan F., Topf A., et al.

JOURNAL OF NEUROMUSCULAR DISEASES , vol.6, no.3, pp.377-384, 2019 (SCI-Expanded, Scopus)

2019

141. Spinal Muscular Atrophy Results and Comparison of Commonly Used Methods

Koc A., Bora E., Yiş U., Giray Bozkaya Ö., Ülgenalp A.

GAZI MEDICAL JOURNAL , vol.30, no.4, pp.381-383, 2019 (ESCI, Scopus)

2019

142. Family functioning and child behavioral problems with Duchenne/Becker muscular dystrophy: A cross-sectional study

TURAN S., ÜLGENALP A., MEMİŞ H., YİŞ U., AKAY A.

Journal of Surgery and Medicine , vol.3, no.7, pp.515-519, 2019 (Peer-Reviewed Journal)

2018

143. Acanthocytosis and HyperCKemia

YİŞ U., Becker K., YILMAZ Ş., Cirak S.

TURKISH JOURNAL OF HEMATOLOGY , vol.35, no.4, pp.296-297, 2018 (SCI-Expanded, Scopus, TRDizin)

2018

144. Hypertrophic Neuropathy of the Sciatic Nerve

YİŞ U., Arslan M., Gulleryuz H.

PEDIATRIC NEUROLOGY , vol.87, pp.77, 2018 (SCI-Expanded, Scopus)

2018

145. Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome

Ghosh S. G., Becker K., Huang H., Salazar T. D., Chai G., Salpietro V., et al.

AMERICAN JOURNAL OF HUMAN GENETICS , vol.103, no.3, pp.431-439, 2018 (SCI-Expanded, Scopus)

2018

146. Targeted sequencing with expanded gene profile enables high diagnostic yield in non-5q-spinal muscular atrophies

Karakaya M., Storbeck M., Strathmann E. A., Delle Vedove A., Hoelker I., Altmueller J., et al.

HUMAN MUTATION , vol.39, no.9, pp.1284-1298, 2018 (SCI-Expanded, Scopus)

2018

147. Childhood onset limb-girdle muscular dystrophies in the Aegean part of Turkey.

YİŞ U., Diniz G., Hazan F., Daimagüler H. S., Baysal B. T., Baydan F., et al.

Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology , vol.37, no.3, pp.210-220, 2018 (Scopus)

2018

148. Changes of primary headache related white matter lesions in pediatric patients

Bayram E., YİŞ U., Paketci G., Okur D., Polat I., Cakmakci H., et al.

TURKISH JOURNAL OF PEDIATRICS , vol.60, no.4, pp.380-384, 2018 (SCI-Expanded, Scopus, TRDizin)

2018

149. Evaluation of the body composition with bioelectrical impedence analysia in epileptic patients treated with valproic acid

Bayram E., TORUN BAYRAM M., YİŞ U., Kurul S. H.

NEUROLOGY ASIA , vol.23, no.2, pp.131-136, 2018 (SCI-Expanded, Scopus)

2018

150. A boy with neck weakness

YİŞ U., Becker K., Cirak S.

NEUROMUSCULAR DISORDERS , vol.28, no.3, pp.236-237, 2018 (SCI-Expanded, Scopus)

2018

151. Genotype-phenotype correlation in novel form of PYROXD1-related congenitalmyopathy

GÜNGÖR S., YİŞ U., ASLAN M., DAİMAGÜLER H. S., BECKER K., TALİM B., et al.

Acta miyologica , 2018 (Peer-Reviewed Journal)

2017

152. Characteristics of pediatric multiple sclerosis: The Turkish pediatric multiple sclerosis database

Yılmaz Ü., Anlar B., GÜCÜYENER K., Yaramış A., CANSU A., Ünalp A., et al.

EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.21, no.6, pp.864-872, 2017 (SCI-Expanded, Scopus)

2017

153. Common and variable clinical, histological, and imaging findings of recessive RYR1-related centronuclear myopathy patients

Neto O. A., Martins Moreno C. d. A., Malfatti E., Donkervoort S., Bohm J., Guimaraes J. B., et al.

NEUROMUSCULAR DISORDERS , vol.27, no.11, pp.975-985, 2017 (SCI-Expanded, Scopus)

2017

154. Neurodevelopmental Disorders Caused by De Novo Variants in KCNB1 Genotypes and Phenotypes

de Kovel C. G. F., Syrbe S., Brilstra E. H., Verbeek N., Kerr B., Dubbs H., et al.

JAMA NEUROLOGY , vol.74, no.10, pp.1228-1236, 2017 (SCI-Expanded, Scopus)

2017

155. Biallelic MCM3AP mutations cause Charcot-Marie-Tooth neuropathy with variable clinical presentation

Karakaya M., Mazaheri N., Polat I., Bharucha-Goebel D., Donkervoort S., Maroofian R., et al.

BRAIN , vol.140, 2017 (SCI-Expanded, Scopus)

2017

156. PRUNE1: a disease-causing gene for secondary microcephaly

Karakaya M., Yilmaz S., Storbeck M., Hoelker I., Heller R., Serdaroglu G., et al.

BRAIN , vol.140, 2017 (SCI-Expanded, Scopus)

2017

157. Association of a synonymous SCN1B variant affecting splicing efficiency with Benign Familial Infantile Epilepsy (BFIE)

Usluer S., Kayserili M. A., Eken A. G., YİŞ U., Leu C., Altmueller J., et al.

EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.21, no.5, pp.773-782, 2017 (SCI-Expanded, Scopus)

2017

158. Expanding spectrum of SCN1A-related phenotype with novel mutations

Hiz-Kurul S., Gursoy S., Ayanoglu M., YİŞ U., Ercal D.

TURKISH JOURNAL OF PEDIATRICS , vol.59, no.5, pp.570-575, 2017 (SCI-Expanded, Scopus, TRDizin)

2017

159. Genetic Landscape of Congenital Myasthenic Syndromes From Turkey: Novel Mutations and Clinical Insights

YİŞ U., Becker K., Kurul S. H., Uyanik G., Bayram E., Haliloglu G., et al.

JOURNAL OF CHILD NEUROLOGY , vol.32, no.8, pp.759-765, 2017 (SCI-Expanded, Scopus)

2017

160. Occipital cortex dysgenesis with white matter changes due to mutations in Laminin alpha 2

YİŞ U., Dixit V., Isikay S., Karakaya M., Baydan F., Diniz G., et al.

TURKISH JOURNAL OF PEDIATRICS , vol.59, no.3, pp.338-341, 2017 (SCI-Expanded, Scopus, TRDizin)

2017

161. Recessive mutations in SLC35A3 cause early onset epileptic encephalopathy with skeletal defects

Marini C., Hardies K., Pisano T., May P., Weckhuysen S., Cellini E., et al.

American Journal of Medical Genetics, Part A , vol.173, no.4, pp.1119-1123, 2017 (SCI-Expanded, Scopus)

2017

162. Dropped head congenital muscular dystrophy caused by de novo mutations in LMNA

KARAOĞLU P., Quizon N., Pergande M., Wang H., Polat A. İ., Ersen A., et al.

BRAIN & DEVELOPMENT , vol.39, no.4, pp.361-364, 2017 (SCI-Expanded, Scopus)

2017

163. A novel mutation in the glycine decarboxylase gene in patient with non-ketotic hyperglycinemia

Kose E., YİŞ U., HIZ A. S., ARSLAN N.

NEUROSCIENCES , vol.22, no.2, pp.131-133, 2017 (SCI-Expanded, Scopus)

2016

164. Increased Wnt and Notch signaling: a clue to the renal disease in Schimke immuno-osseous dysplasia?

Morimoto M., Myung C., Beirnes K., Choi K., Asakura Y., Bokenkamp A., et al.

ORPHANET JOURNAL OF RARE DISEASES , vol.11, 2016 (SCI-Expanded, Scopus)

2016

165. Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy

Mignot C., von Stuelpnagel C., Nava C., Ville D., Sanlaville D., Lesca G., et al.

JOURNAL OF MEDICAL GENETICS , vol.53, no.8, pp.511-522, 2016 (SCI-Expanded, Scopus)

2016

166. SCN1A gene sequencing in 46 Turkish epilepsy patients disclosed 12 novel mutations

Usluer S., Salar S., Arslan M., YİŞ U., KARA B., Tekturk P., et al.

SEIZURE-EUROPEAN JOURNAL OF EPILEPSY , vol.39, pp.34-43, 2016 (SCI-Expanded, Scopus)

2016

167. Schwartz-Jampel syndrome with gastroduodenal bleeding

Polat I., KARAOĞLU P., YİŞ U., Kurul S. H.

JOURNAL OF PEDIATRIC NEUROSCIENCES , vol.11, no.3, pp.255-257, 2016 (ESCI, Scopus)

2016

168. Myelin Oligodendrocyte Glycoprotein Antibody Persistency in a Steroid-Dependent ADEM Case

Polat I., YİŞ U., KARAOĞLU P., Ayanoglu M., Ozturk T., GÜLERYÜZ UÇAR H., et al.

PEDIATRICS , vol.137, no.5, 2016 (SCI-Expanded, Scopus)

2016

169. Posterior reversible leukoencephalopathy syndrome with spinal cord involvement in a 9-year-old girl

YİŞ U., KARAOĞLU P., Kurul S. H., SOYLU A., Cakmakci H., KAVUKÇU S.

BRAIN & DEVELOPMENT , vol.38, no.1, pp.154-157, 2016 (SCI-Expanded, Scopus)

2016

170. Importance of Skin Changes in the Differential Diagnosis of Congenital Muscular Dystrophies

YİŞ U., Baydan F., Karakaya M., Kurul S. H., Cirak S.

BIOMED RESEARCH INTERNATIONAL , vol.2016, 2016 (SCI-Expanded, Scopus)

2016

171. Nerve Conduction Studies in Children with Subclinical Hypothyroidism

Catli G., YİŞ U., Tuhan H. U., Ayanoglu M., HIZ A. S., BÖBER E., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.86, pp.493, 2016 (SCI-Expanded, Scopus)

2015

172. Quality of Life and Sleep in Children Diagnosed with Duchenne Muscular Dystrophy and Their Mothers' Level of Anxiety: a Case-Control Study

Ozyurt G., Bayram E., Karaoglu P., Kurul S. H., YİŞ U.

DUSUNEN ADAM-JOURNAL OF PSYCHIATRY AND NEUROLOGICAL SCIENCES , vol.28, no.4, pp.362-368, 2015 (ESCI, Scopus, TRDizin)

2015

173. An infant with hypomotor seizures and cutaneous lesions

YİŞ U., Ayanoglu M., Polat A. İ., GÜLERYÜZ UÇAR H., Kurul S. H.

ACTA NEUROLOGICA BELGICA , vol.115, no.4, pp.687-688, 2015 (SCI-Expanded, Scopus)

2015

174. A Multinational Survey on Actual Diagnostics and Treatment of Subacute Sclerosing Panencephalitis

Haeusler M., Aksoy A., Alber M., ALTUNBAŞAK Ş., Angay A., Arsene O. T., et al.

NEUROPEDIATRICS , vol.46, no.6, pp.377-384, 2015 (SCI-Expanded, Scopus)

2015

175. Lack of IL7R alpha expression in T cells is a hallmark of T-cell immunodeficiency in Schimke immuno-osseous dysplasia (SIOD)

Sanyal M., Morimoto M., Baradaran-Heravi A., Choi K., Kambham N., Jensen K., et al.

CLINICAL IMMUNOLOGY , vol.161, no.2, pp.355-365, 2015 (SCI-Expanded, Scopus)

2015

176. An 11-Year-Old Boy with Headache, Fever, and Neck Pain

YİŞ U., Polat I., KARAOĞLU P., Ayanaoglu M., Unsal E., ÖZKÜTÜK A. A., et al.

PEDIATRIC ANNALS , vol.44, no.10, pp.426-432, 2015 (SCI-Expanded, Scopus)

2015

177. A novel NTRK1 mutation in a patient with congenital insensitivity to pain with anhidrosis

YİŞ U., Mademan I., KAVUKÇU S., Baets J.

ACTA NEUROLOGICA BELGICA , vol.115, no.3, pp.509-511, 2015 (SCI-Expanded, Scopus)

2015

178. Importance of neurologic and cutaneous signs in the diagnosis of Schimke immuno-osseous dysplasia

Polat A. İ., YİŞ U., Ayanoglu M., HIZ A. S., GÜLERYÜZ UÇAR H., Ozturk-Atasoy T., et al.

TURKISH JOURNAL OF PEDIATRICS , vol.57, no.5, pp.509-513, 2015 (SCI-Expanded, Scopus, TRDizin)

2015

179. Williams Syndrome with Infantile Spasms

Polat I., KARAOĞLU P., Ayanoglu M., YİŞ U., HIZ A. S.

INDIAN JOURNAL OF PEDIATRICS , vol.82, no.8, pp.757-758, 2015 (SCI-Expanded, Scopus)

2015

180. Juvenile Myasthenia Gravis: A Report of Three Cases and Literature Review

Yilmaz U., YİŞ U.

JOURNAL OF CLINICAL AND ANALYTICAL MEDICINE , vol.6, no.4, pp.473-478, 2015 (ESCI, Scopus, TRDizin)

2015

181. Life-Threatening and Rare Adverse Effects of Phenytoin

Polat I., KARAOĞLU P., Ayanoglu M., YİŞ U., HIZ A. S.

PEDIATRIC EMERGENCY CARE , vol.31, no.7, 2015 (SCI-Expanded, Scopus)

2015

182. Cytomegalovirus associated diffuse encephalomyelitis in a healthy child

Yis R., YİŞ U., ÇARMAN K. B., Gunes N., Akar E., Derundere U.

IZMIR DR BEHCET UZ COCUK HASTANESI DERGISI , vol.5, no.1, pp.69-74, 2015 (ESCI, TRDizin)

2015

183. Parieto-occipital encephalomalacia in children; clinical and electrophysiological features of twenty-seven cases

KARAOĞLU P., Polat A. I., YİŞ U., Hiz S.

JOURNAL OF PEDIATRIC NEUROSCIENCES , vol.10, no.2, pp.103-107, 2015 (ESCI, Scopus)

2015

184. Lissencephaly With Brainstem and Cerebellar Hypoplasia and Congenital Cataracts

YİŞ U.

JOURNAL OF CHILD NEUROLOGY , vol.30, no.5, pp.625-626, 2015 (SCI-Expanded, Scopus)

2015

185. A Novel Mutation in the Mitochondrial DNA Cytochrome b Gene (MTCYB) in a Patient with Prader Willi Syndrome

YİŞ U., EZGÜ F. S., Karakaya P., Polat I., ARSLAN N., Çankaya T., et al.

JOURNAL OF CHILD NEUROLOGY , vol.30, no.3, pp.378-381, 2015 (SCI-Expanded, Scopus)

2015

186. Importance of acrocyanosis in delayed walking

YİŞ U., Polat I., Karakaya P., Ayanoglu M., HIZ A. S.

JOURNAL OF PEDIATRIC NEUROSCIENCES , vol.10, no.1, pp.80-81, 2015 (ESCI, Scopus)

2015

187. Sağlikli Bir Çocukta Sitomegalovirüs İlişkili Diffüz Ensefalomyelit

reyhan y., YİŞ U., ÇARMAN K. B., necibe g., akar e., ümit d.

İzmir Dr. Behçet Uz Çocuk Hastanesi Dergisi , 2015 (TRDizin)

2015

188. Expression Patterns of Micro-RNAs 146a, 181a, and 155 in Subacute Sclerosing Panencephalitis

YİŞ U., Tufekci U. K., GENÇ Ş., ÇARMAN K. B., Bayram E., Topcu Y., et al.

JOURNAL OF CHILD NEUROLOGY , vol.30, no.1, pp.69-74, 2015 (SCI-Expanded, Scopus)

2015

189. Klippel Treunanay Syndrome in differential diagnosis of cerebral palsy

pakize k., yasemin t., BAYRAM E., YİŞ U., GÜLERYÜZ H., HIZ A. S.

Journal of Dr. Behcet Uz Children's Hospital , 2015 (Peer-Reviewed Journal)

2015

190. Quality of Life and Sleep in Children Diagnosed with Duchenne Muscular Dystrophy and Their Mothers’xx Level of Anxiety: a Case-Control Study

ÖZYURT G., BAYRAM E., KARAOĞLU P., HIZ A. S., YİŞ U.

JOURNAL OF PSYCHIATRY AND NEUROLOGICAL SCIENCES , 2015 (Scopus, TRDizin)

2014

191. Evaluation of vitamin D status in children with refractory epilepsy

KARAOĞLU P., POLAT A. İ., AYANOĞLU M., YİŞ U., HIZ A. S.

IZMIR DR BEHCET UZ COCUK HASTANESI DERGISI , vol.4, no.3, pp.167-170, 2014 (ESCI, TRDizin)

2014

192. Fisher-Bickerstaff syndrome with negative anti-ganglioside antibody test results associated with mycoplasma pneumoniae infection

YİŞ U., KARAOĞLU P., POLAT A. İ., AYANOĞLU M., GÜLERYÜZ UÇAR H., HIZ A. S.

IZMIR DR BEHCET UZ COCUK HASTANESI DERGISI , vol.4, no.3, pp.218-222, 2014 (TRDizin)

2014

193. A case of acute post-streptococcal glomerulonephritis that developed posterior reversible encephalopathy syndrome

Kasap B., ÇARMAN K. B., YİŞ U.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , vol.49, no.4, pp.348-352, 2014 (ESCI, Scopus, TRDizin)

2014

194. The Paediatric migraine disability assessment score is a useful tool for evaluating prophylactic migraine treatment

Topcu Y., Kurul S. H., Bayram E., Sozmen K., YİŞ U.

ACTA PAEDIATRICA , vol.103, no.11, 2014 (SCI-Expanded, Scopus)

2014

195. Zonisamide attenuates hyperoxia-induced apoptosis in the developing rat brain

Topcu Y., Bayram E., ÖZBAL S., YİŞ U., TUĞYAN K., KARAOĞLU P., et al.

NEUROLOGICAL SCIENCES , vol.35, no.11, pp.1769-1775, 2014 (SCI-Expanded, Scopus)

2014

196. Capillary Malformation-Arteriovenous Malformation Syndrome with Spinal Involvement

YİŞ U., Kurul S. H., GÜLERYÜZ UÇAR H., MEN S.

PEDIATRIC DERMATOLOGY , vol.31, no.6, pp.744-746, 2014 (SCI-Expanded, Scopus)

2014

197. Importance of acylcarnitine profile analysis for disorders of lipid metabolism in adolescent patients with recurrent rhabdomyolysis: Report of two cases

Topcu Y., Bayram E., KARAOĞLU P., YİŞ U., Kurul S. H.

ANNALS OF INDIAN ACADEMY OF NEUROLOGY , vol.17, no.4, pp.437-440, 2014 (SCI-Expanded, Scopus)

2014

198. Transient striatal involvement with frequent seizures and fast recovery associated with Mycoplasma pneumoniae infection

YİŞ U., KARAOĞLU P., POLAT A. İ., GÜLERYÜZ UÇAR H., HIZ A. S.

IZMIR DR BEHCET UZ COCUK HASTANESI DERGISI , vol.4, no.2, pp.135-138, 2014 (ESCI, TRDizin)

2014

199. Effects of Hyperglycemia on the Developing Brain in Newborns

Tayman C., YİŞ U., Hirfanoglu I., Oztekin O., GÖKTAŞ G., Bilgin B. C.

PEDIATRIC NEUROLOGY , vol.51, no.2, pp.239-245, 2014 (SCI-Expanded, Scopus)

2014

200. The efficacy and safety of levetiracetam in paediatric patients treated with chemotherapeutic agents for haematologic disorders

Bayram E., Topcu Y., TÜFEKÇİ Ö., KARAOĞLU P., YİŞ U., ÖREN H., et al.

JOURNAL OF PAEDIATRICS AND CHILD HEALTH , vol.50, no.7, pp.553-556, 2014 (SCI-Expanded, Scopus)

2014

201. Clinical, Radiological, and Genetic Survey of Patients With Muscle-Eye-Brain Disease Caused by Mutations in POMGNT1

YİŞ U., Uyanik G., Rosendahl D. M., ÇARMAN K. B., Bayram E., Heise M., et al.

PEDIATRIC NEUROLOGY , vol.50, no.5, pp.491-497, 2014 (SCI-Expanded, Scopus)

2014

202. Carnitine Palmitoyl Transferase II Deficiency in an Adolescent Presenting With Rhabdomyolysis and Acute Renal Failure

Topcu Y., Bayram E., KARAOĞLU P., YİŞ U., Bayram M., Kurul S. H.

PEDIATRIC EMERGENCY CARE , vol.30, no.5, pp.343-344, 2014 (SCI-Expanded, Scopus)

2014

203. A novel activating ABCC8 mutation underlying neonatal diabetes mellitus in an infant presenting with cerebral sinovenous thrombosis

Anik A., Catli G., ABACI A., YİŞ U., ÖREN H., GÜLERYÜZ UÇAR H., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.27, pp.533-537, 2014 (SCI-Expanded, Scopus)

2014

204. Severe Neurologic Involvement of Degos Disease in a Pediatric Patient

KARAOĞLU P., Topcu Y., Bayram E., YİŞ U., AKARSU S., Atalay E., et al.

JOURNAL OF CHILD NEUROLOGY , vol.29, no.4, pp.550-554, 2014 (SCI-Expanded, Scopus)

2014

205. Folik asit eksikliğine bağlı ciddi aksonal nöropati gelişen restriktif tip anoreksiya nervoza tanılı bir olgu

BAYRAM E., YİŞ U., ÖZTURA İ., AKDOĞAN Ö., TOPÇU Y., KARAOĞLU P., et al.

Journal of Dr. Behcet Uz Children's Hospital , vol.4, no.1, pp.72-74, 2014 (TRDizin)

2014

206. Frank-Ter Haar Sendromlu Bir Olgu

POLAT A. İ., KARAOĞLU P., AYANOĞLU M., YİŞ U., HIZ A. S.

Pediatri Uzmanlık Akademisi Dergisi , vol.2, no.2, pp.11-13, 2014 (Peer-Reviewed Journal)

2014

207. Poor Clinical Outcome In A Good Controlled Neonatal Citrullinemia Patient

BAYRAM E., SEVER A. H., KARAOĞLU P., TOPÇU Y., YİŞ U., GÜLERYÜZ UÇAR H., et al.

Dokuz Eylül Üniversitesi Tıp Fakültesi Dergisi , vol.28, no.1, pp.31-36, 2014 (TRDizin)

2014

208. Comparison of Cranial Magnetic Resonance Imaging Findings and Clinical Features in Patients with Corpus Callosum Abnormalities

Bayram E., Topcu Y., YİŞ U., Cakmaci H., Kurul S. H.

NEUROPEDIATRICS , vol.45, no.1, pp.30-35, 2014 (SCI-Expanded, Scopus)

2014

209. Measurement of the apparent diffusion coefficient in paediatric mitochondrial encephalopathy cases and a comparison of parenchymal changes associated with the disease using follow-up diffusion coefficient measurements

Uysal F., Cakmakci H., YİŞ U., ELLİDOKUZ H., HIZ A. S.

EUROPEAN JOURNAL OF RADIOLOGY , vol.83, no.1, pp.212-218, 2014 (SCI-Expanded, Scopus)

2014

210. Chronic Spinal Epidural Hematoma

YİŞ U., KALEMCİ O., Polat I., KARAOĞLU P., ÖZTURA İ., GÜLERYÜZ UÇAR H., et al.

JOURNAL OF PEDIATRICS , vol.164, no.1, pp.215-216, 2014 (SCI-Expanded, Scopus)

2014

211. Clinical features and psychomotor development at one year of age in infants born from a mother with chorioamnionitis

HIZ A. S., YİŞ U., ÖZER E., KARAOĞLU P., POLAT A. İ.

IZMIR DR BEHCET UZ COCUK HASTANESI DERGISI , vol.4, no.1, pp.15-19, 2014 (ESCI, TRDizin)

2014

212. Importance of Diazepam Administration During Electroencephalography in the Differential Diagnosis of Cortical Visual Loss

YİŞ U., Topcu Y., Bayram E., Karakaya P., Cakmakci H., Kurul S. H.

JOURNAL OF CHILD NEUROLOGY , vol.29, no.1, pp.114-117, 2014 (SCI-Expanded, Scopus)

2014

213. Rotavirüs gastroenteriti ile ilişkili süt çocuğunun benign afebril konvülziyonları: olguların değerlendirilmesi

TOPÇU Y., BAYRAM E., KARAOĞLU P., YİŞ U., HIZ A. S.

Pediatri Uzmanlık Akademisi Dergisi , vol.2, no.1, pp.12-16, 2014 (Peer-Reviewed Journal)

2014

214. Clinical syndromes or ciliopathies associated with molar tooth sign

YİŞ U., Dirik M. A., Dirik E.

Pediatric Neurology , vol.50, no.6, 2014 (SCI-Expanded, Scopus)

2014

215. Psychomotor Retardation Caused by a Defective Thyroid Hormone Transporter: Report of Two Families with Different MCT8 Mutations

Anik A., Kersseboom S., DEMİR K., Catli G., YİŞ U., BÖBER E., et al.

HORMONE RESEARCH IN PAEDIATRICS , vol.82, no.4, pp.261-271, 2014 (SCI-Expanded, Scopus)

2014

216. Do antispasmodics affect the body composition and basal metabolic rate in patients with cerebral palsy?

Bayram E., Topcu Y., ŞAHİN E., YİŞ U., Peker O., ARSLAN N., et al.

Paediatria Croatica , vol.58, no.2, pp.95-100, 2014 (SCI-Expanded, Scopus)

2013

217. Molar Tooth Sign Is Not Pathognomonic for Joubert Syndrome

Dirik M. A., YİŞ U., Dirik E.

PEDIATRIC NEUROLOGY , vol.49, no.6, pp.515-516, 2013 (SCI-Expanded, Scopus)

2013

218. Involuntary Movements Misdiagnosed as Seizure During Vitamin B₁₂ Treatment

ÇARMAN K. B., Belgemen T., YİŞ U.

PEDIATRIC EMERGENCY CARE , vol.29, no.11, pp.1223-1224, 2013 (SCI-Expanded, Scopus)

2013

219. Caffeic acid phenethyl ester prevents apoptotic cell death in the developing rat brain after pentylenetetrazole-induced status epilepticus

YİŞ U., Topcu Y., ÖZBAL S., TUĞYAN K., Bayram E., Karakaya P., et al.

EPILEPSY & BEHAVIOR , vol.29, no.2, pp.275-280, 2013 (SCI-Expanded, Scopus)

2013

220. The Utility of Head Up Tilt Test with Video Electroencephalography in Children with Recurrent Loss of Consciousness

Bayram E., Topcu Y., Yilmaz N., Karakaya P., Kir M., Yis U., et al.

HONG KONG JOURNAL OF PAEDIATRICS , vol.18, no.4, pp.217-222, 2013 (SCI-Expanded, Scopus)

2013

221. The combination of thermal dysregulation and agenesis of corpus callosum: Shapiro's or/and reverse Shapiro's syndrome

Topcu Y., Bayram E., KARAOĞLU P., YİŞ U., Kurul S. H.

ANNALS OF INDIAN ACADEMY OF NEUROLOGY , vol.16, no.4, pp.716-719, 2013 (SCI-Expanded, Scopus)

2013

222. Polysomnographic and long-term video electroencephalographic evaluation of cases presenting with parasomnias

YİŞ U., Kurul S. H., ÖZTURA İ., ECEVİT M. C., Dirik E.

ACTA NEUROLOGICA BELGICA , vol.113, no.3, pp.285-289, 2013 (SCI-Expanded, Scopus)

2013

223. Kabuki syndrome and perisylvian cortical dysplasia in a Turkish girl

Topcu Y., Bayram E., KARAOĞLU P., YİŞ U., Kurul S. H.

JOURNAL OF PEDIATRIC NEUROSCIENCES , vol.8, no.3, pp.259-260, 2013 (ESCI, Scopus)

2013

224. Reply to the author: The measurement of carotid intima media thickness precisely and accurately for evaluating epileptic children treated with oxcarbazepine

YİŞ U., Dogan M.

BRAIN & DEVELOPMENT , vol.35, no.7, pp.695-696, 2013 (SCI-Expanded, Scopus)

2013

225. Phrenic Nerve Palsy Associated With Brachial Plexus Avulsion in a Pediatric Patient With Multitrauma

KARAOĞLU P., YİŞ U., ÖZTURA İ., Akdogan O., Bayram E., Topcu Y., et al.

PEDIATRIC EMERGENCY CARE , vol.29, no.8, pp.922-923, 2013 (SCI-Expanded, Scopus)

2013

226. Rolandik Epilepsi Her Zaman Selim Bir Hastalık mıdır?

BAYRAM E., TOPÇU Y., KARAOĞLU P., YİŞ U., HIZ A. S.

Dokuz Eylül Üniversitesi Tıp Fakültesi Dergisi , vol.27, no.2, pp.91-94, 2013 (TRDizin)

2013

227. Epilepsi tanısıyla izlenen hastalar ve annelerinde uyku kalitesinin değerlendirilmesi

BAYRAM E., TOPÇU Y., KARAOĞLU P., YİŞ U., HIZ A. S.

IZMIR DR BEHCET UZ COCUK HASTANESI DERGISI , vol.3, no.2, pp.87-92, 2013 (TRDizin)

2013

228. Correlation between motor performance scales, body composition, and anthropometry in patients with duchenne muscular dystrophy

Bayram E., Topcu Y., Karakaya P., Torun Bayram M., Şahin E., Erdinc Gunduz N., et al.

ACTA NEUROLOGICA BELGICA , vol.113, no.2, pp.133-137, 2013 (SCI-Expanded, Scopus)

2013

229. Incidental White Matter Lesions in Children Presentng With Headache

Bayram E., Topcu Y., KARAOĞLU P., YİŞ U., GÜLERYÜZ UÇAR H., Kurul S. H.

HEADACHE , vol.53, no.6, pp.970-976, 2013 (SCI-Expanded, Scopus)

2013

230. Hepatitis A infection presenting with recurrent seizures and widespread cerebral white matter lesions

YİŞ U., Çarman K. B., Yilmaz-Çiftdoǧan D., Yildirim C., Yiş R., Akar E.

Turkish Journal of Pediatrics , vol.55, no.1, pp.118-120, 2013 (SCI-Expanded, Scopus)

2013

231. Van der Knaap hastalığı: Olgu sunumu

BAYRAM E., TOPÇU Y., KARAOĞLU P., YİŞ U., GÜLERYÜZ UÇAR H., HIZ A. S.

Journal of Dr. Behcet Uz Children's Hospital , vol.3, no.1, pp.60-62, 2013 (TRDizin)

2013

232. A novel mutation in the sodium channel alpha 1 subunit gene in a child with Dravet syndrome in Turkey

Arslan M., YİŞ U., Caglayan H., Akin R.

NEURAL REGENERATION RESEARCH , vol.8, no.10, pp.955-958, 2013 (SCI-Expanded, Scopus)

2013

233. A case of atypical Miller Fisher syndrome with negative anti-GQ1b immunoglobulin G and importance of H reflex

YİŞ U., Bayram E., Topcu Y., Karakaya P., Hiz-Kurul S.

TURKISH JOURNAL OF PEDIATRICS , vol.55, no.2, pp.235-236, 2013 (SCI-Expanded, Scopus)

2013

234. Coexistence of myositis, transverse myelitis, and Guillain Barré syndrome following Mycoplasma pneumoniae infection in an adolescent

Topcu Y., Bayram E., KARAOĞLU P., YİŞ U., Guleryuz H., Kurul S. H.

Journal of Pediatric Neurosciences , vol.8, no.1, pp.59-63, 2013 (SCI-Expanded, Scopus)

2013

235. Evaluation of the cases with Friedreich ataxia

Kurul S. H., YİŞ U., Güzel A. i., KASAP H., Başak N., Dirik E.

Gulhane Medical Journal , vol.55, no.2, pp.123-127, 2013 (Scopus, TRDizin)

2013

236. Evaluation of awake electroencephalography findings in children with attention deficit hyperactivity disorder before psychostimulant treatment

Bayram E., Topcu Y., Karaarslan D., Akinci G., YİŞ U., AKAY A., et al.

Paediatria Croatica , vol.57, no.1, pp.57-60, 2013 (SCI-Expanded, Scopus)

2013

237. Molybdenum cofactor deficiency: Review of 12 cases (MoCD and review)

Bayram E., Topcu Y., Karakaya P., YİŞ U., Cakmakci H., Ichida K., et al.

EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.17, no.1, pp.1-6, 2013 (SCI-Expanded, Scopus)

2013

238. Acute Cervical Dystonia After the First Dose of Butamirate Citrate

Bayram E., Karakaya P., Topcu Y., YİŞ U., HIZ A. S.

PEDIATRIC EMERGENCY CARE , vol.29, no.1, pp.80-81, 2013 (SCI-Expanded, Scopus)

2012

239. Brain magnetic resonance imaging findings suggestive of widespread white matter involvement in children with Streptococcus mitis meningitis

YİŞ U., Çarman K. B., Yiş R., Derundere Ü.

Turkish Journal of Pediatrics , vol.54, no.4, pp.425-428, 2012 (SCI-Expanded, Scopus)

2012

240. Pneumatosis intestinalis due to rotavirus infection in a child with Prader-Willi syndrome

Yis U., Topcu Y., Bayram E., Karakaya P., Cakmakci H., Hiz-Kurul S.

TURKISH JOURNAL OF PEDIATRICS , vol.54, no.6, pp.679-681, 2012 (SCI-Expanded, Scopus)

2012

241. MYOPATHIC CHANGES IN MUSCLE BIOPSY OF A PATIENT WITH INFANTILE SYSTEMIC HYALINOSIS

Bayram E., Topcu Y., Karakaya P., Firat C., YİŞ U., ÖZER E., et al.

PAEDIATRIA CROATICA , vol.56, no.4, pp.301-304, 2012 (SCI-Expanded, Scopus)

2012

242. Ring chromosome 21 in the differential diagnosis of waddling gait

Arslan M., YİŞ U., Vurucu S., Tunca Y., Unay B., Akin R.

BRAIN & DEVELOPMENT , vol.34, no.9, pp.792-795, 2012 (SCI-Expanded, Scopus)

2012

243. Silent cerebral infarct in child patients with beta thalassaemia intermedia

Leblebisatan G., Bay A., Sirikci A., Kilincaslan H., Sonmezisik S., Leblebisatan S., et al.

Blood Coagulation and Fibrinolysis , vol.23, no.7, pp.608-613, 2012 (SCI-Expanded, Scopus)

2012

244. Acquired epileptiform opercular syndrome: F-18 fluorodeoxyglucose positron emission tomography (FDG-PET) findings and efficacy of levetiracetam therapy

Arslan M., YİŞ U., Vurucu S., Ince S., Unay B., Akin R.

EPILEPSY & BEHAVIOR , vol.25, no.1, pp.50-53, 2012 (SCI-Expanded, Scopus)

2012

245. Makrosefali ayırıcı tanısında Canavan hastalığı: Olgu sunumu

BAYRAM E., TOPÇU Y., KARAOĞLU P., YİŞ U., GÜLERYÜZ UÇAR H., HIZ A. S.

Journal of Dr. Behcet Uz Children's Hospital , vol.2, no.2, pp.107-110, 2012 (TRDizin)

2012

246. Evaluation of cases with impaired state of consciousness: Gaziantep Children's Hospital experience

YİŞ U., Yüksel Ç. N., Köse A., Erdoǧan S.

Turkish Journal of Pediatrics , vol.54, no.1, pp.30-34, 2012 (SCI-Expanded, Scopus)

2012

247. Sjögren-Larsson syndrome: Report of monozygote twins and a case with a novel mutation

YİŞ U., Terrinoni A.

Turkish Journal of Pediatrics , vol.54, no.1, pp.64-66, 2012 (SCI-Expanded, Scopus)

2012

248. Status dystonicus and rhabdomyolysis in a patient with subacute sclerosing panencephalitis

YİŞ U.

Turkish Journal of Pediatrics , vol.54, no.1, pp.90-91, 2012 (SCI-Expanded, Scopus)

2012

249. Neuroprotective effects of recombinant human erythropoietin in the developing brain of rat after lithium-pilocarpine induced status epilepticus

Sozmen S. C., Kurul S. H., Yis U., TUĞYAN K., BAYKARA B., YILMAZ O.

BRAIN & DEVELOPMENT , vol.34, no.3, pp.189-195, 2012 (SCI-Expanded, Scopus)

2012

250. Effects of oxcarbazepine treatment on serum lipids and carotid intima media thickness in children

YİŞ U., Dogan M.

BRAIN & DEVELOPMENT , vol.34, no.3, pp.185-188, 2012 (SCI-Expanded, Scopus)

2011

251. Heterogeneity of Marinesco-Sjogren Syndrome: Report of Two Cases

Yis U., Cirak S., HIZ A. S., Cakmakci H., Dirik E.

PEDIATRIC NEUROLOGY , vol.45, no.6, pp.409-411, 2011 (SCI-Expanded, Scopus)

2011

252. Acute motor axonal neuropathy and H1N1 influenza a infection

Yiş R., YİŞ U., Yüksel Ç. N., Erdoǧan S., YILMAZ M.

Turkish Journal of Pediatrics , vol.53, no.6, pp.715-716, 2011 (SCI-Expanded, Scopus)

2011

253. Fibromuscular dysplasia as a cause of stroke in a 9-year-old girl

Yis U., MEN S., Cakmakci H., Demircioglu F., Kurul S. H., ÖREN H., et al.

TURKISH JOURNAL OF PEDIATRICS , vol.53, no.5, pp.567-570, 2011 (SCI-Expanded, Scopus)

2011

254. Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy and PEHO-like syndrome: Report of two cases

Yis U., Hiz S., Anal O., Dirik E.

JOURNAL OF PEDIATRIC NEUROSCIENCES , vol.6, no.2, pp.165-168, 2011 (ESCI, Scopus)

2011

255. Obstructive hydrocephalus resulting from cerebral venous thrombosis

Leblebisatan G., YİŞ U., Dogan M., Derundere U.

JOURNAL OF PEDIATRIC NEUROSCIENCES , vol.6, no.2, pp.129-130, 2011 (ESCI, Scopus)

2011

256. Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation

Rohrbach M., Vandersteen A., YİŞ U., Serdaroglu G., Ataman E., Chopra M., et al.

ORPHANET JOURNAL OF RARE DISEASES , vol.6, 2011 (SCI-Expanded, Scopus)

2011

257. Defects in amphiphysin 2 (BIN1) and triads in several forms of centronuclear myopathies

Toussaint A., Cowling B. S., Hnia K., Mohr M., Oldfors A., Schwab Y., et al.

ACTA NEUROPATHOLOGICA , vol.121, no.2, pp.253-266, 2011 (SCI-Expanded, Scopus)

2011

258. Fukutin mutations in non-Japanese patients with congenital muscular dystrophy: Less severe mutations predominate in patients with a non-Walker-Warburg phenotype

Yis U., Uyanik G., Heck P. B., Smitka M., Nobel H., Ebinger F., et al.

NEUROMUSCULAR DISORDERS , vol.21, no.1, pp.20-30, 2011 (SCI-Expanded, Scopus)

2011

259. [Meningitis and white matter lesions due to Streptococcus mitis in a previously healthy child]. Önceden Saǧlikli Bir Çocukta Streptococcus mitis'e Baǧli Menenjit ve Beyaz Cevher Lezyonlari

Yiş R., Yüksel C. N., Derundere U., YİŞ U.

Mikrobiyoloji bülteni , vol.45, no.4, pp.741-745, 2011 (SCI-Expanded, Scopus, TRDizin)

2010

260. Case report of intrafamilial variability in autosomal recessive centronuclear myopathy associated to a novel BIN1 stop mutation

Boehm J., Yis U., Ortac R., Cakmakci H., Kurul S. H., Dirik E., et al.

ORPHANET JOURNAL OF RARE DISEASES , vol.5, 2010 (SCI-Expanded, Scopus)

2010

261. Late infantile neuronal ceroid lipofuscinosis: A case reports

Yis U., Kurul S. H., Ozogul C., Dirik E.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , vol.45, no.2, pp.155-157, 2010 (SCI-Expanded, Scopus, TRDizin)

2010

262. Diagnostic value of proton MR spectroscopy and diffusion-weighted MR imaging in childhood inherited neurometabolic brain diseases and review of the literature

Cakmakci H., Pekcevik Y., YİŞ U., Unalp A., Kurul S.

EUROPEAN JOURNAL OF RADIOLOGY , vol.74, no.3, 2010 (SCI-Expanded, Scopus)

2010

263. Evaluation of cases with subacute sclerosing panencephalitis

YİŞ U., Erdogan S., Bastemir M.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , vol.45, no.1, pp.49-52, 2010 (SCI-Expanded, Scopus, TRDizin)

2010

264. Two cases with megalencephalic leukoencephalopathy with subcortical cysts and MLC1 mutations in the Turkish population

Yis U., Scheper G. C., Uran N., Unalp A., Cakmakci H., Hiz-Kurul S., et al.

TURKISH JOURNAL OF PEDIATRICS , vol.52, no.2, pp.179-183, 2010 (SCI-Expanded, Scopus)

2010

265. The relation of serum ghrelin, leptin and insulin levels to the growth patterns and feeding characteristics in breast-fed versus formula-fed infants

YİŞ U., ÖZTÜRK Y., Sisman A., UYSAL S., Soylu O. B., BÜYÜKGEBİZ B.

TURKISH JOURNAL OF PEDIATRICS , vol.52, no.1, pp.35-41, 2010 (SCI-Expanded, Scopus)

2010

266. Late infantile neuronal ceroid lipofuscinosis: A case report Geç infantil nöronal seroid lipofusinoz: Bir olgu sunumu

YİŞ U., HIZ A. S., Özoǧul C., Dirik E.

Turk Pediatri Arsivi , vol.45, no.2, pp.155-157, 2010 (Scopus, TRDizin)

2010

267. Evaluation of cases with subacute sclerosing panencephalitis Subakut sklerozan panansefalit tanisi ile izlenen hastalarimizin deǧerlendirilmesi

YİŞ U., Erdoǧan S., Baştemir M.

Turk Pediatri Arsivi , vol.45, no.1, pp.49-52, 2010 (Scopus, TRDizin)

2010

268. Rhabdomyolysis Associated With Olanzapine Treatment in a Child With Autism

Karakaya P., YİŞ U., Kurul S. H., Tuerkmen M. A.

PEDIATRIC EMERGENCY CARE , vol.26, no.1, pp.41-42, 2010 (SCI-Expanded, Scopus)

2009

269. Metabolic Alterations During Valproic Acid Treatment: A Prospective Study

ABACI A., Saygi M., YİŞ U., DEMİR K., Dirik E., BÖBER E.

PEDIATRIC NEUROLOGY , vol.41, no.6, pp.435-439, 2009 (SCI-Expanded, Scopus)

2009

270. Evaluation of serum lipids and carotid artery intima media thickness in epileptic children treated with valproic acid

Erdemir A., Cullu N., YİŞ U., Demircioglu F., KIR M., Cakmakci H., et al.

BRAIN & DEVELOPMENT , vol.31, no.10, pp.713-716, 2009 (SCI-Expanded, Scopus)

2009

271. Dentatorubral pallidoluysian atrophy in a Turkish family

Yis U., Dirik E., Gundogdu-Eken A., Basak A. N.

TURKISH JOURNAL OF PEDIATRICS , vol.51, no.6, pp.610-612, 2009 (SCI-Expanded, Scopus)

2009

272. Unusual findings in Leigh syndrome caused by T8993C mutation

YİŞ U., Seneca S., Dirik E., Kurul S. H., ÖZER E., Cakmakci H., et al.

EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.13, no.6, pp.550-552, 2009 (SCI-Expanded, Scopus)

2009

273. Clinical, pathological and radiological survey of patients with Leigh syndrome.

YİŞ U., Hiz Kurul S., Dirik E., Çakmakçi H., ÖZER E.

Minerva pediatrica , vol.61, no.4, pp.371-8, 2009 (Scopus)

2009

274. Temporary Diazepam Responsive Apneic Attacks and Congenital Myasthenic Syndrome

Yis U., Kurul S. H., ÖZTURA İ., Ozden O., Akinci G., Dirik E.

JOURNAL OF CHILD NEUROLOGY , vol.24, no.7, pp.895-898, 2009 (SCI-Expanded, Scopus)

2009

275. The relationship of neonatal subclinical electrographic seizures to neurodevelopmental outcome at 1 year of age

Kurul S. H., Sutcuoglu S., YİŞ U., DUMAN N., KUMRAL A., ÖZKAN H.

JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE , vol.22, no.7, pp.584-588, 2009 (SCI-Expanded, Scopus)

2009

276. Two Young Sisters with Spinocerebellar Ataxia Type 2 Showing Different Clinical Progression of Disease

Yis U., Dirik E., Kurul S. H., Eken A. G., Basak A. N.

CEREBELLUM , vol.8, no.2, pp.127-129, 2009 (SCI-Expanded, Scopus)

2009

277. Effects of epilepsy and valproic acid on oxidant status in children with idiopathic epilepsy

YİŞ U., Seckin E., Kurul S. H., Kuralay F., Dirik E.

EPILEPSY RESEARCH , vol.84, no.2-3, pp.232-237, 2009 (SCI-Expanded, Scopus)

2009

278. Benign paroxysmal torticollis

Demirpence S., YİŞ U., Kurul S. H.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , vol.44, no.1, pp.35-37, 2009 (SCI-Expanded, Scopus, TRDizin)

2009

279. Evaluation of cases with congenital muscular dystrophy

Yis U., Uyanik G., Kurul S. H., Cakmakci H., Ozer E., Dirik E., et al.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , vol.44, no.1, pp.23-28, 2009 (SCI-Expanded, Scopus, TRDizin)

2009

280. Nonketotic Hyperglycinemia and Acquired Hydrocephalus

Yis U., Kurul S. H., Dirik E.

PEDIATRIC NEUROLOGY , vol.40, no.2, pp.138-140, 2009 (SCI-Expanded, Scopus)

2009

281. Protective Effects of Topiramate against Hyperoxic Brain Injury in the Developing Brain

Kurul S. H., Yis U., Kumral A., Tugyan K., Cilaker S., KOLATAN H. E., et al.

NEUROPEDIATRICS , vol.40, no.1, pp.22-27, 2009 (SCI-Expanded, Scopus)

2009

282. Congenital Perislyvian Syndrome; Report Of Three Cases

YİŞ U., Batemir M.

EUROPEAN JOURNAL OF THERAPEUTICS , vol.15, no.3, pp.23-25, 2009 (ESCI)

2009

283. Oxidant Status in Children After Febrile Seizures

Gunes S., Dirik E., YİŞ U., Seckin E., Kuralay F., Kose S., et al.

PEDIATRIC NEUROLOGY , vol.40, no.1, pp.47-49, 2009 (SCI-Expanded, Scopus)

2009

284. Diffuse myelitis in a 9-month-old infant: case report and review of the literature.

Hüdaoglu O., YİŞ U., Kurul S., Çakmakçi H., Saygi M., Dirik E.

Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit , vol.15, no.1, pp.230-4, 2009 (Scopus)

2008

285. Effect of erythropoietin on oxygen-induced brain injury in the newborn rat

YİŞ U., Kurul S. H., KUMRAL A., TUĞYAN K., CİLAKER MIÇILI S., YILMAZ O., et al.

NEUROSCIENCE LETTERS , vol.448, no.3, pp.245-249, 2008 (SCI-Expanded, Scopus)

2008

286. Dystrophin knockdown mice suggest that early, transient dystrophin expression might be enough to prevent later pathology Response

Giunta C., YİŞ U., Steinmann B.

NEUROMUSCULAR DISORDERS , vol.18, no.11, pp.907, 2008 (SCI-Expanded, Scopus)

2008

287. Hyperoxic exposure leads to cell death in the developing brain

YİŞ U., Kurul S. H., KUMRAL A., CİLAKER MIÇILI S., TUĞYAN K., GENÇ Ş., et al.

BRAIN & DEVELOPMENT , vol.30, no.9, pp.556-562, 2008 (SCI-Expanded, Scopus)

2008

288. Mycoplasma pneumoniae: nervous system complications in childhood and review of the literature

YİŞ U., Kurul S. H., Cakmakci H., Dirik E.

EUROPEAN JOURNAL OF PEDIATRICS , vol.167, no.9, pp.973-978, 2008 (SCI-Expanded, Scopus)

2008

289. Acute Cerebellitis with Cerebellar Swelling Successfully Treated with Standard Dexamethasone Treatment

YİŞ U., Kurul S. H., Cakmacki H., Dirik E.

CEREBELLUM , vol.7, no.3, pp.430-432, 2008 (SCI-Expanded, Scopus)

2008

290. Cetirizine-induced dystonic reaction in a 6-year-old boy

Esen I., Demirpence S., YİŞ U., Kurul S.

PEDIATRIC EMERGENCY CARE , vol.24, no.9, pp.627-628, 2008 (SCI-Expanded, Scopus)

2008

291. Vertebral artery dissection in a patient with Wildervanck syndrome

Dirik E., YİŞ U., Dirik M. A., Cakmakci H., Men S.

PEDIATRIC NEUROLOGY , vol.39, no.3, pp.218-220, 2008 (SCI-Expanded, Scopus)

2008

292. Long-standing fever and Angelman syndrome: Report of two cases

YİŞ U., Giray Ö., Kurul S. H., BORA E., ÜLGENALP A., Ercal D., et al.

JOURNAL OF PAEDIATRICS AND CHILD HEALTH , vol.44, no.5, pp.308-310, 2008 (SCI-Expanded, Scopus)

2008

293. Multiple sulfatase deficiency in a Turkish family resulting from a novel mutation

YİŞ U., Pepe S., Kurul S. H., Ballabio A., Cosma M. P., Dirik E.

BRAIN & DEVELOPMENT , vol.30, no.5, pp.374-377, 2008 (SCI-Expanded, Scopus)

2008

294. Recurrent attacks of status epilepticus as predominant symptom in 3-methylcrotonyl-CoA carboxylase deficiency

Dirik E., YİŞ U., Pasaoglu G., Chambaz C., Baumgartner M. R.

BRAIN & DEVELOPMENT , vol.30, no.3, pp.218-220, 2008 (SCI-Expanded, Scopus)

2008

295. Differential diagnosis of muscular hypotonia in infants: The kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VI)

YİŞ U., Dirik E., Chambaz C., Steinmann B., Giunta C.

NEUROMUSCULAR DISORDERS , vol.18, no.3, pp.210-214, 2008 (SCI-Expanded, Scopus)

2007

296. Homocysteine levels in epileptic children receiving antiepileptic drugs

Kurul S., Uenalp A., YİŞ U.

JOURNAL OF CHILD NEUROLOGY , vol.22, no.12, pp.1389-1392, 2007 (SCI-Expanded, Scopus)

2007

297. Serum and urine cystatin C levels in children with post-pyelonephritic renal scarring: a pilot study

İŞLEKEL G. H., SOYLU A., ALTUN Z. S., Yis U., Turkmen M., Kavukcu S.

INTERNATIONAL UROLOGY AND NEPHROLOGY , vol.39, no.4, pp.1241-1250, 2007 (SCI-Expanded, Scopus)

2007

298. Spinocerebellar ataxia type 2 in a Turkish family

Dirik E., Yis U., Basak N., Soydan E., Huedaoglu O., Oezgoenuel F.

JOURNAL OF CHILD NEUROLOGY , vol.22, no.7, pp.891-894, 2007 (SCI-Expanded, Scopus)

2007

299. Basilar artery thrombosis in a child heterozygous for prothrombin gene G20210A mutation

Hudaoglu O., Kurul S., Yis U., Dirik E., Cakmakci H., Men S.

JOURNAL OF CHILD NEUROLOGY , vol.22, no.3, pp.329-331, 2007 (SCI-Expanded, Scopus)

2007

300. A case of Walker-Warburg syndrome resulting from a homozygous POMT1 mutation

Yis U., Uyanik G., Kurul S., Dirik E., Ozer E., Gross C., et al.

EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , vol.11, no.1, pp.46-49, 2007 (SCI-Expanded, Scopus)

2006

301. Nonconvulsive status epilepticus and neurodevelopmental delay

Dirik E., Yis U., Hudaoglu O., Kurul S.

PEDIATRIC NEUROLOGY , vol.35, no.3, pp.209-212, 2006 (SCI-Expanded, Scopus)

2006

302. Parental attitude of mothers, iron deficiency anemia, and breath-holding spells

Hudaoglu O., Dirik E., Yis U., Kurul S.

PEDIATRIC NEUROLOGY , vol.35, no.1, pp.18-20, 2006 (SCI-Expanded, Scopus)

2006

303. Aorta coarctation presenting with intracranial aneurysm rupture

Huedaoglu O., Kurul S., Cakmakci H., Men S., Yis U., Dirik E.

JOURNAL OF PAEDIATRICS AND CHILD HEALTH , vol.42, no.7-8, pp.477-479, 2006 (SCI-Expanded, Scopus)

2006

304. **Multiple erythematous nodules and ecthyma gangrenosum as a manifestation of Pseudomonas aeruginosa sepsis in a previously healthy infant**

Duman M., Ozdemir D., Yis U., Koroglu T., Oren O., Berktas S.

PEDIATRIC DERMATOLOGY , vol.23, no.3, pp.243-246, 2006 (SCI-Expanded, Scopus)

2006

305. Diabetic neuropathic cachexia in a girl with type 1 diabetes mellitus

Atas A., ABACI A., Unuvar T., Uluc Y., Bober E., Buyukgebiz A.

HORMONE RESEARCH , vol.65, pp.60, 2006 (SCI-Expanded)

2005

306. Recurrent parotitis in a seven year-old boy [5]

YİŞ U., Ünal N.

Indian Pediatrics , vol.42, no.9, pp.958-959, 2005 (SCI-Expanded, Scopus)

2005

307. Recurrent parotitis in a seven year-old boy

Yis U., Unal N.

INDIAN PEDIATRICS , vol.42, no.9, pp.958-959, 2005 (SCI-Expanded, Scopus)

2005

308. Primary lymphedema in a four- year-old boy [5]

YİŞ U., Dirik E.

Indian Pediatrics , vol.42, no.7, pp.726-728, 2005 (SCI-Expanded, Scopus)

2005

309. Primary lymphedema in a four-year-old boy

Yis U., Dirik E.

INDIAN PEDIATRICS , vol.42, no.7, pp.726-728, 2005 (SCI-Expanded, Scopus)

2005

310. Metoclopramide induced dystonia in children: two case reports

YİŞ U., Ozdemir D., DUMAN M., Unal N.

EUROPEAN JOURNAL OF EMERGENCY MEDICINE , vol.12, no.3, pp.117-119, 2005 (SCI-Expanded, Scopus)

2005

311. Ghrelin: A new hormon in energy metabolism Ghrelin: Enerji metabolizmasinin düzenlenmesinde yeni bir hormon

YİŞ U., Öztürk Y., Büyükgebiz B.

Cocuk Sagligi ve Hastaliklari Dergisi , vol.48, no.2, pp.196-201, 2005 (Scopus)

Papers Presented at Peer-Reviewed Scientific Conferences

2025

1. Uncovering hidden causes in developmental epileptic encephalopathy: high resolution structural variant detection with optical genome mapping

Yilmaz S. K., Durmusalioglu E. A., Dogan D. E. T., Kanmaz S., Atik T., Mutlu M. B., et al.

58th Conference of the European-Society-of-Human-Genetics (ESHG), Milan, Italy, 24 - 27 May 2025, vol.33, pp.791, (Summary Text)

2025

2. FRAGILE X SYNDROME IN CHILDREN WITH DEVELOPMENTAL DELAY: A SIX-YEAR SINGLE-CENTER EXPERIENCE

SÜNCAK S., GÜRSOY S., ÇAĞLAYAN A. O., YİŞ U., HIZ A. S., ÖZTÜRK YILMAZ Ş., et al.

2. Uluslararası Katılımlı İzmir Pediatri Kongresi, İzmir, Turkey, 11 - 13 September 2025, pp.109, (Summary Text)

2024

3. A national plan of action to raise awareness and improve medical care of Duchenne muscular Dystrophy (AIM-DMD)

Akinci G., Coskun A., Koken O., Ardicli D., Cinar E., Okur T., et al.

29th International Congress of the World-Muscle-Society (WMS), Prague, Czech Republic, 8 - 12 October 2024, vol.43, (Summary Text)

2024

4. PIEZO2-associated distal arthrogryposis: phenotypic spectrum and genotypephenotype correlations in a multicenter case series

Akinci G., Cinar E., Gunay C., Ardicli D., Degerliyurt A., Ozyilmaz B., et al.

29th International Congress of the World-Muscle-Society (WMS), Prague, Czech Republic, 8 - 12 October 2024, vol.43, (Summary Text)

2024

5. WITH 10 YEARS OF EXPERIENCE: THE ROLE OF ANTIEPILEPTIC TREATMENT AND LEVETIRACETAM IN VLBW INFANTS

ARMAĞAN C., NİŞANCI B., HALK M., YİŞ U., HIZ A. S., ERDOĞAN F., et al.

Best Practice in Neonatology, 1st joint UENPS and EFCNI congress, Ljubljana, Slovenia, 3 - 05 July 2024, (Summary Text)

2024

6. Nadir Bir Hipotoni Nedeni; S-Adenosilhomosistein Hidrolaz Eksikliği

KULU B., TEKE KISA P., KARALAR PEKUZ Ö. K., HALK M., YİŞ U., ARSLAN N.

XVII. ULUSLARARASI KATILIMLI METABOLİK HASTALIKLAR VE BESLENME KONGRESİ, Antalya, Turkey, 28 April 2024, (Summary Text)

2024

7. 10 YILLIK DENEYİMLE: VLBW BEBEKLERDE ANTİEPİLEPTİK TEDAVİ VE LEVETİRASETAMIN ROLÜ

ARMAĞAN C., NİŞANCI B., HALK M., ERDOĞAN F., YİŞ U., HIZ A. S., et al.

31. Ulusal Neonatoloji Kongresi, Antalya, Turkey, 24 April 2024, (Summary Text)

2024

8. NEONATAL HİPOKSİK İSKEMİK ENSEFALOPATİ: HAFİF EVRE HASTALARIN NÖROLOJİK PROGNOZU VE TEDAVİ STRATEJİLERİNİN ANALİZİ

CANBELDEK M., ARMAĞAN C., ŞENOL H. B., BAYKARA H. B., BAYKARA A. B., GÜLERYÜZ UÇAR H., et al.

31. Ulusal Neonatoloji Kongresi, Antalya, Turkey, 24 April 2024, (Summary Text)

2023

9. A new nationwide initiative to explore genetic variants in a large Turkish hereditary neuropathy cohort

Akinci G., Ozyilmaz B., Parlar O., Unalp A., Polat I., Baydan F., et al.

28th International Annual Congress of the World-Muscle-Society (WMS), Charlestown, Saint Kitts And Nevis, 3 - 07 October 2023, vol.33, (Summary Text)

2023

10. MALİGN ORTA SEREBRAL ARTER ENFARKTÜSÜ İÇİN ERKEN DEKOMPRESİF KRANİEKTOMİ: İKİ PEDİATRİK OLGU

Gök A., Soydemir D., Arslan G., Erişik N. Ö., Yılmaz M., Kızmazoğlu C., et al.

Türk Nöroradyoloji Derneği Ulusal 32. Yıl Kongresi, İstanbul, Turkey, 24 - 26 March 2023, pp.90-91, (Summary Text)

2023

11. AKUT GÖRME KAYBI OLAN ÇOCUKLARIN NÖROLOJİK AÇIDAN DEĞERLENDİRİLMESİ: TEK MERKEZLİ BEŞ YILLIK DENEYİM

Gök A., Üstebay D. Ü., Aykol D., Öztürk A. T., Aydın A., Hız A. S., et al.

IX. Erciyes Pediatri Akademisi Kongresi ve I. Uluslararası Katılımlı Erciyes Türk Dünyası Çocuk Nörolojisi Kongresi, Kayseri, Turkey, 15 - 19 March 2023, pp.131-132, (Full Text)

2022

12. Evaluation of Sleep with “Brief Infant Sleep Questionnaire” in Children with Cerebral Palsy

Günay Ç., Hız A. S., Yiş U., Aydın A.

3rd International Eurasian Social Pediatrics Annual Congress and the 7th National Social Pediatrics Annual Congress, İzmir, Turkey, 16 - 20 November 2022, pp.130, (Summary Text)

2022

13. Vinkristin Tedavisi Gören Kanserli Çocuklarda Vinkristin ile İlişkili Periferal Nöropatinin Değerlendirilmesi: Türkçe Geçerlik Güvenirlik Çalışması

ÖZDEMİR B., ÖZALP GERÇEKER G., ÖZDEMİR E. Z., Yıldırım B. G., YİŞ U., GÜNAY Ç., et al.

3. Uluslararası Akdeniz Pediatri Hemşireliği Kongresi, Ankara, Turkey, 12 - 15 October 2022, (Summary Text)

2022

14. Vinkristin Alan Çocuklarda Vinkristin ile İlişkili Periferal Nöropatinin Değerlendirilmesi: Türkçe Geçerlik Güvenirlik Çalışması

Özdemir B., Özalp Gerçeker G., Özdemir E. Z., Yıldırım B. G., Yiş U., Günay Ç., et al.

3rd International Mediterranean Pediatric Nursing Congress, Antalya, Turkey, 12 - 15 October 2022, (Unpublished)

2022

15. A rare dual pathology: Idiopathic intracranial hypertension presenting with isolated unilateral facial nerve palsy

Gök A., Üstebay D. Ü., Hız A. S., Yiş U.

17th International Child Neurology Congress, Antalya, Turkey, 3 - 07 October 2022, pp.737, (Summary Text)

2022

16. Cases with Seizures During Routine Video Electroencephalography: Clinical and Electroencephalographic Characteristics

Gök A., Günay Ç., Aykol D., Yeşilmen M. C., Hız A. S., Yiş U.

17th International Child Neurology Congress, Antalya, Turkey, 3 - 07 October 2022, pp.550, (Summary Text)

2022

17. Electromyography in Pediatric Population, A Single Center Experience

Aykol D., Üstebay D. Ü., Günay Ç., Gök A., Karakaya Ö., Hız A. S., et al.

17th international child neurology congress, ICNC2022, Antalya, Turkey, 3 - 07 October 2022, pp.20-21, (Full Text)

2022

18. CASE REPORT: DOCK7 MUTATION AS A RARE CAUSE OF EPILEPTIC ENCEPHALOPATHY, CORTICAL BLINDNESS, DYSMORPHIC FINDINGS

Özsoy Ö., Soydemir D., Günay Ç., Sarıkaya Uzan G., Yeşilmen M. C., Hız A. S., et al.

17th International Child Neurology Congress , Antalya, Turkey, 3 - 07 October 2022, pp.20-30, (Summary Text)

2022

19. A case of first pediatric pseudotumor cerebri syndrome secondary to superior sagittal sinus thrombosis associated with SARS-CoV-2

Yeşilmen M. C., Günay Ç., Sarıkaya Uzan G., Özsoy Ö., Hız A. S., Yiş U.

17th International Child Neurology Congress, Antalya, Turkey, 2 October - 07 November 2022, pp.26-27, (Summary Text)

2022

20. Levetiracetam Monotherapy For The Treatment Of Febrile and Febrile Induced Seizures

Sarıkaya Uzan G., Paketçi C., Hız A. S., Yiş U.

17th International Chil Neurology Congress, Antalya, Turkey, 2 October - 07 November 2022, pp.27-28, (Summary Text)

2022

21. Pontocerebellar Hypoplasia Associated With TTC 1 Mutation: Case Series

Sarıkaya Uzan G., Sönmezler E., Hız A. S., Günay Ç., Oktay Y., Hovarth R., et al.

17th International Child Neurology Congress, Antalya, Turkey, 2 - 07 October 2022, pp.25-26, (Summary Text)

2022

22. A SYSTEMATIC APPROACH IN DIAGNOSIS OF HYPOTONIC INFANT: REPORT OF 7 CASE

Gök A., Özsoy Ö., Çinleti T., Hız A. S., Yiş U.

2.Doğu Pediatri Kongresi, Diyarbakır, Turkey, 29 September - 02 October 2022, pp.239, (Summary Text)

2022

23. PEDİATRİK OPTİK NÖRİT TANILI HASTALARIN DEĞERLENDİRİLMESİ- ON YILLIK TEK MERKEZ DENEYİMİ

Özsoy Ö., Hız A. S., Yiş U.

4. Uluslararası Dr. Behçet Uz Çocuk Kongresi, İzmir, Turkey, 22 - 24 September 2022, pp.46, (Full Text)

2022

24. Dikkat Eksikliği ve Hiperaktivite Bozukluğu Tanılı Olgularda Nörolojik Komorbiditelerinin Değerlendirilmesi

Yeşilmen M. C., Sarıkaya Uzan G., Hız A. S., Yiş U.

4. Uluslararası Dr. Behçet Uz Çocuk Kongresi, İzmir, Turkey, 22 - 24 September 2022, pp.1-2, (Summary Text)

2022

25. Juvenil miyoklonik epilepsi tanılı hastaların demografik, klinik ve elektroensefalografik değerlendirilmesi- Tek merkez deneyimi

Yeşilmen M. C., Özsoy Ö., Günay Ç., Sarıkaya Uzan G., Hız A. S., Yiş U.

23. Dokuz Eylül Pediatri Günleri, İzmir, Turkey, 14 - 16 September 2022, pp.14-15, (Summary Text)

2022

26. Sekonder mitokondriyal disfonksiyon ile giden polinöropatili olgularımızın değerlendirilmesi

Yeşilmen M. C., Günay Ç., Hız A. S., Yiş U.

16. Uluslararası katılımlı metabolik hastalıklar ve beslenme kongresi, Hatay, Turkey, 28 April - 01 June 2022, pp.378, (Summary Text)

2022

27. The investigation of the effects of a novel missense mutation in the KATNAL2 gene in patient fibroblasts and fibroblast-derived cells using functional analysis methods

Hız A. S., Sönmezler Adalı E., Ekinci B., Yaraş T., Yiş U., Yaramış A., et al.

4. Uluslararsı Katılımlı Hücre Ölümü Araştırma Derneği Kongresi, 17 - 19 March 2022, pp.1, (Full Text)

2021

28. Pediatrik Modifiye Total Nöropati Skoru: Kanserli Çocuklarda Kemoterapi ile İlişkili Periferik Nöropati Skalasının Psikometrik Özellikleri

Özalp Gerçeker G., Özdemir B., Özdemir E. Z., Yıldırım B. G., Yiş U., Günay Ç., et al.

65. Türkiye Milli Pediatri Kongresi, 20. Milli Çocuk Hemşireliği Kongresi, Antalya, Turkey, 3 - 07 November 2021, (Unpublished)

2021

29. Çocukluk çağının sentrotemporal dikenli epilepsisinde başlangıç hemogram parametreleri prognoz üzerine etkili olabilir mi?

Günay Ç., Özsoy Ö., Sarıkaya Uzan G., Hız A. S., Yiş U.

23. Ulusal Çocuk Nörolojisi Kongresi, İzmir, Turkey, 27 - 31 October 2021, pp.101, (Summary Text)

2021

30. Olgu Sunumu: Serebellar Atrofinin Nadir Bir Nedeni PTPMT1 Gen Mutasyonu Olabilir mi?

Sönmezler E., Özsoy Ö., Sarıkaya Uzan G., Günay Ç., Yiş U., Oktay Y., et al.

23. Ulusal Çocuk Nörolojisi Kongresi, İzmir, Turkey, 27 - 31 October 2021, (Unpublished)

2021

31. Tip 3 Spinal Muskuler Atrofi (SMA) ‘li Olguda Genotip - Fenotip İlişkisi

Üstebay D. Ü., Aykol D., Gök A., Yılmaz Uzman C., Ülgenalp A., Hız A. S., et al.

23. ulusal çocuk nöroloji kongresi, İzmir, Turkey, 27 - 31 October 2021, pp.118, (Full Text)

2021

32. Limb-Girdle Müsküler Distrofi Tanısında Genetik Panel

Sarıkaya Uzan G., Yılmaz Uzman C., Çinleti T., Ülgenalp A., Hız A. S., Yiş U.

5. NÖROMÜSKÜLER HASTALIKLAR KONGRESİ, Samsun, Turkey, 24 - 26 September 2021, pp.11-12, (Summary Text)

2021

33. Miyastenia Gravis Hastalarımızın Değerlendirilmesi

Özsoy Ö., Günay Ç., Sarıkaya Uzan G., Hız A. S., Yiş U.

V. Nöromusküler Hastalıklar Kongresi, Samsun, Turkey, 24 - 26 September 2021, pp.14, (Summary Text)

2021

34. Bir Olgu Üzerinden Sıcak Su Epilepsisi ve Tedavisi

Günay Ç., Özsoy Ö., Sarıkaya Uzan G., Hız A. S., Yiş U.

3. Uluslarası Dr Behçet Uz Çocuk Kongresi, İzmir, Turkey, 23 - 25 September 2021, (Unpublished)

2021

35. Başağrısı Nedeniyle Çocuk Nöroloji Polikliniğine Başvuran Olguların B12 Düzeylerinin Değerlendirilmesi

Özsoy Ö., Sarıkaya Uzan G., Günay Ç., Hız A. S., Yiş U.

3. Uluslararası Dr Behçet Uz Çocuk Kongresi, İzmir, Turkey, 23 - 25 September 2021, pp.130, (Summary Text)

2021

36. Kırmızı Kulak Sendromu - Üç Pediyatrik Olgu

Günay Ç., Sarıkaya Uzan G., Özsoy Ö., Hız A. S., Erdağ T. K., Olgun Y., et al.

3. Uluslararası Dr. Behçet Uz Çocuk Kongresi, İzmir, Turkey, 23 - 25 September 2021, pp.1, (Summary Text)

2021

37. SANTRAL SİNİR SİSTEMİ EDİNSEL DEMİYELİNİZAN HASTALIK TANILI HASTALARIMIZIN DEĞERLENDİRİLMESİ

Aykol D., Üstebay D. Ü., Gök A., Hız A. S., Yiş U.

Aydın Pediatri Derneği 1. Pediatri Çevrimiçi Sempozyumu, Aydın, Turkey, 29 May 2021, pp.54-55, (Full Text)

2013

38. Konvülziyon ile başvuran infantil diyabet olgusunda serebral iskemi ve venöz sinüs trombozu

KARAOĞLU P., ANIK A., ÇATLI G., ABACI A., YİŞ U., BÖBER E., et al.

15. Ulusal Çocuk Nörolojisi Kongresi, Sivas, Turkey, 22 May 2013, pp.108-109, (Summary Text)

2021

39. Komplike Febril Nöbette Elektroensefalografi Ne Kadar Gerekli?

Sarıkaya Uzan G., Günay Ç., Hız A. S., Yiş U.

Cerrahpaşa Pediatri Günleri - Semptomdan Tanıya, İstanbul, Turkey, 15 - 18 April 2021, pp.121, (Summary Text)

2021

40. Nöbet mi, Değil mi?

Günay Ç., Sarıkaya Uzan G., Özsoy Ö., Hız A. S., Yiş U.

7. Erciyes Pediatri Akademisi Kış Kongresi, Kayseri, Turkey, 26 - 27 March 2021, pp.218-222, (Full Text)

2022

41. Çocuk Nöroloji Polikliniğinde Kreatin Kinaz Yüksekliği Saptanan Hastaların İncelenmesi

Gök A., Soydemir D., Günay Ç., Gürsoy Doruk Ö., Hız A. S., Yiş U.

Dokuz Eylül Üniversitesi Tıp Fakültesi, 22. Pediatri Günleri ve 3. Pediatri Hemşireliği Günleri, İzmir, Turkey, 25 - 27 March 2022, pp.1-2, (Summary Text)

2021

42. Pediatrik Psödotümör Serebri Tanılı Hastalarımızın Değerlendirilmesi

Aykol D., Üstebay D. Ü., Sarıkaya Uzan G., Özsoy Ö., Hız A. S., Yiş U.

22. pediatri günleri ve 3. pediatri hemşireliği günleri, İzmir, Turkey, 25 - 27 March 2021, pp.31-32, (Full Text)

2021

43. Bayılma: Ne sıklıkta nörolojik?

Günay Ç., Sarıkaya Uzan G., Hız A. S., Yiş U.

6. Genç Pediatristler Kongresi, İstanbul, Turkey, 5 - 07 March 2021, pp.103, (Summary Text)

2021

44. Nöromusküler Tutulum Gösteren Mitokondrial Hastalıklar: 16 Genetik Tanılı Olgunun Retrospektif Değerlendirilmesi

GÜNAY Ç., SOYDEMİR D., SARIKAYA UZAN G., EDEM P., HIZ A. S., YİŞ U., et al.

22. Ulusal Çocuk Nörolojisi Kongresi, Turkey, 27 October 2021 - 01 November 2020, pp.109, (Summary Text)

2020

45. Pediyatrik Nörolojik Aciller: Tek merkez deneyimimiz

Günay Ç., Sarıkaya Uzan G., Soydemir D., Karakaya Ö., Aykol D., Paketçi C., et al.

Sağlıklı Büyüyen Çocuk Kongresi, İzmir, Turkey, 18 - 20 December 2020, pp.175-176, (Summary Text)

2020

46. Nadir bir dual patoloji: Rasmussen Ensefaliti ve Sistemik Lupus Eritematozus Birlikteliği

Gök A., Edem P., Soydemir D., Sarıkaya Uzan G., Günay Ç., Türkuçar S., et al.

22. Ulusal Çocuk Nöroloji Kongresi, İzmir, Turkey, 28 October - 01 November 2020, pp.108, (Summary Text)

2020

47. Tekrarlayan ağrılı oftalmoplejik nöropati: İki olgu

Günay Ç., Soydemir D., Edem P., Sarıkaya Uzan G., Hız A. S., Yiş U., et al.

22. Ulusal Çocuk Nöroloji Kongresi, İzmir, Turkey, 28 October - 01 November 2020, pp.110, (Summary Text)

2020

48. Nadir Bir Erken İnfantil Epileptik Ensefalopati Nedeni; {Gnao1} Gen Mutasyonu

Aykol D., Edem P., Soydemir D., Sarıkaya Uzan G., Günay Ç., Yılmaz Uzman C., et al.

22. Ulusal Çocuk Nöroloji Kongresi, İzmir, Turkey, 28 October - 01 November 2020, pp.107, (Summary Text)

2020

49. IQSEC2 spektrum bozukluğu: Dirençli epileptik nöbet ile seyreden iki olgu

Edem P., Soydemir D., Sarıkaya Uzan G., Günay Ç., Yılmaz Uzman C., Ülgenalp A., et al.

22. Ulusal Çocuk Nöroloji Kongresi, İzmir, Turkey, 28 October - 01 November 2020, pp.111, (Summary Text)

2020

50. Nöromusküler tutulum gösteren mitokondriyal hastalıklar: 16 genetik tanılı olgunun retrospektif değerlendirilmesi

Günay Ç., Soydemir D., Sarıkaya Uzan G., Edem P., Hız A. S., Yiş U., et al.

22. Ulusal Çocuk Nöroloji Kongresi, İzmir, Turkey, 28 October - 01 November 2020, pp.109, (Summary Text)

2020

51. Nadir Bir Dual Patoloji: Rasmusen Ensefaliti Ve Sistemik Lupus Eritematozus Birlikteliği

Gök A., Soydemir D., Sarıkaya Uzan G., Günay Ç., Türkuçar S., Hız A. S., et al.

22.Ulusal Çocuk Nörolojisi Kongresi, İzmir, Turkey, 28 October - 01 November 2020, pp.108, (Summary Text)

2020

52. Persistan miyelin oligodendrosit glikoprotein antikoru pozitifliği olan olgu

POLAT A. İ., AYANOĞLU M., YİŞ U., HIZ A. S.

17. Ulusal Çocuk Nöroloji Kongresi, Turkey, 6 - 09 May 2020, (Summary Text)

2020

53. Çocukluk Çağı Nöropsikiyatrik Komorbiditelerinin Değerlendirilmesi: 5 Yıllık Tek Merkez Deneyimi

Sarıkaya Uzan G., Paketçi C., Yiş U.

2. Uluslararası Dr.Behçet Uz 2.Çocuk Kongresi 4-7 Mart 2020 Swissotel Büyük Efes, İzmir, İzmir, Turkey, 05 March 2020, pp.12, (Full Text)

2019

54. BECKER MUSKULER DİSTROFİLİ BİR OLGUDA STİMÜLAYONLUBİOFEEDBACK EĞİTİMİNİN FONKSİYONEL SEVİYE VE DENGEÜZERİNE ETKİSİ

KURT M., savaş d., TARSUSLU ŞİMŞEK T., YİŞ U.

5. Uluslararası Pediatrik Fizyoterapi Kongresi, 21 - 23 November 2019, (Summary Text)

2019

55. DUCHENNE MUSKULER DISTROFILI BIR OLGUDA SANALGERÇEKLİK EĞİTİMİNİN FONKSİYONEL SEVİYE, KAS KUVVETİ VEDENGE ÜZERİNE ETKİSİ

KURT M., savaş d., TARSUSLU ŞİMŞEK T., YİŞ U.

5. Uluslararası Pediatrik Rehabilitasyon Kongresi, 21 - 23 November 2019, (Summary Text)

2022

56. Pontoserebellar Hipoplazi Nedeni Olarak Cask Gen Mutasyonu

Sarıkaya Uzan G., Paketçi C., Edem P., Soydemir D., Yiş U., Oktay Y., et al.

II. Mersin Çocuk Nörolojisi Kış Sempozyumu, Mersin, Turkey, 8 - 09 November 2022, pp.34, (Summary Text)

2019

57. Pontoserebellar Hipoplazi Nedeni Olarak Cask Gen Mutasyonu

SARIKAYA UZAN G., PAKETÇİ C., EDEM P., SOYDEMİR D., YİŞ U., OKTAY Y., et al.

II. Mersin Çocuk Nörolojisi Kış Sempozyumu, Mersin, Turkey, 8 - 09 November 2019, pp.34, (Summary Text)

2019

58. Nusinersen Tedavisi Alan Spinal Müsküler Atrofi Tanılı Hastalarımızın Değerlendirilmesi

Sarıkaya Uzan G., Edem P., Soydemir D., Paketçi C., Alataş Ö., Men S., et al.

3. Nöromüsküler Hastalıklar Kongresi, 1-3 Kasım 2019 Çeşme/İzmir, İzmir, Turkey, 1 - 03 November 2019, pp.32, (Summary Text)

2019

59. NÖROFİBROMATOSİS OLGULARININ KLİNİK, GENETİK ÖZELLİKLERİVE 2 YENİ VARYANTIN TANIMLANMASI

YILMAZ C., KOÇ A., YİŞ U., HIZ A. S., GİRAY BOZKAYA Ö., ÜLGENALP A., et al.

4. Ulusal Çocuk Genetik Kongresi, 25 - 27 September 2019, (Full Text)

2019

60. **Severe neurodevelopmental disease caused by a homozygous TLK2 variant**

Topf A., Oktay Y., Balaraju S., Yilmaz E., Sonmezler E., Yis U., et al.

52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg, Sweden, 15 - 18 June 2019, vol.27, pp.1850-1851, (Summary Text)

2019

61. Hypertrophic neuropathy of the sciatic nerve

Yis U., Arslan M., Guleryuz H.

24th International Annual Congress of the World-Muscle-Society (WMS), Copenhagen, Denmark, 1 - 05 October 2019, vol.29, (Summary Text)

2019

62. Identification and characterization of disease-causing genes in non-5q-SMA by next-generation sequencing technology: Lessons learned from NeurOmics study

Karakaya M., Storbeck M., Strathmann E., Delle Vedove A., Hoelker I., Altmueller J., et al.

52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg, Sweden, 15 - 18 June 2019, vol.27, pp.1483-1484, (Summary Text)

2019

63. DCX Heterozigot Mutasyonu İlişkili Nadir Bir Subkortikal Band Heterotopi Olgusu

KOCABEY M., USLUER E., KOÇ A., PAKETÇİ C., YİŞ U., GİRAY BOZKAYA Ö.

4. Ulusal Çocuk Genetik Kongresi, Ankara, Turkey, 25 - 27 September 2019, pp.22, (Summary Text)

2019

64. Acute flaccid Myelitis outbreak through 2016-2018: multicentre experience from Turkey,

ÜNVER O., TÜRKDOĞAN D., GÜLER S., KİPOĞLU O., GÜNGÖR M., PAKETÇİ C., et al.

13th European Paediatric Neurology Society (EPNS) Congress, ATİNA, Greece, 17 - 21 September 2019, (Summary Text)

2019

65. Poretti Boltshauser Syndrome: A Novel Variant in LAMA1 Gene

EDEM P., SARIOĞLU F. C., PAKETÇİ C., BAYRAM E., HIZ A. S., YİŞ U.

13th European Paediatric Neurology Society (EPNS) Congress, Atina, Greece, 17 - 22 September 2019, pp.167, (Summary Text)

2019

66. Herpes Simplex Virus-1 as a Rare Aetiology of Isolated Acute Cerebellitis

PAKETÇİ C., EDEM P., OKUMUŞ C., SARIOĞLU F. C., BAYRAM E., HIZ A. S., et al.

13th European Paediatric Neurology Society (EPNS) Congress, Atina, Greece, 17 - 21 September 2019, pp.211, (Summary Text)

2019

67. Analysis of stroke in neonates and children: Single center experience

ÖREN H., TÜFEKÇİ Ö., YILMAZ Ş., YİŞ U., POLAT A. İ.

XXVII Congress of the International Society on Thrombosis and Haemostasis, 6 - 10 July 2019, (Summary Text)

2019

68. 2016-2018 Akut Flask Myelit Olgular: Çok Merkez Deneyimi,

ÜNVER O., TÜRKDOĞAN D., GÜLER S., KİPOĞLU O., GÜNGÖR M., PAKETÇİ C., et al.

21.Uluslararası Katılımlı Ulusal Çocuk Nörolojisi Kongresi, Muğla, Turkey, 1 - 05 May 2019, (Summary Text)

2019

69. Hipomiyelinizasyon ile birlikte bazal ganglion ve serebellum atrofisi-olgu sunumu

KARAOĞLU P., POLAT A. İ., AYANOĞLU M., GÜLERYÜZ UÇAR H., HIZ A. S., YİŞ U.

21. Uluslararası Katılımlı Ulusal Çocuk Nörolojisi Kongresi, Muğla, Turkey, 01 May 2019, pp.213-214, (Summary Text)

2019

70. Ege Bölgesinde Çocukluk Çağı Başlangıçlı Limb-Girdle Müsküler Distrofilerin İncelenmesi.

ÜNALP A., YİŞ U., TOKLU BAYSAL B., Hazan F., HIZ A. S., AKINCI G.

21. Uluslararası Katılımlı Ulusal Çocuk Nörolojisi Kongresi, 1-5 Mayıs 2019, Hilton Dalaman Sarıgerme Hotel, Muğla., 1 - 05 May 2019, (Summary Text)

2019

71. 2016-2018 Akut flask miyelit olguları: çok merkez deneyimi

ÜNVER O., TÜRKDOĞAN D., GÜLER S., KİPOĞLU O., GÜNGÖR M., PAKETÇİ C., et al.

21. Uluslararası Katılımlı Ulusal Çocuk Nörolojisi Kongresi, Muğla, Turkey, 1 - 05 May 2019, pp.74-75, (Summary Text)

2019

72. Evaluation of Clinical Characteristics of Patients with Glutaric Aciduria Type IIc.

TEKE KISA P., Öztürk Hişmi B., Gülten Arslan z., YİŞ U., ARSLAN N.

Uluslarası Metabolik Hastalıklar ve Beslenme Kongresi, İstanbul, Turkey, 10 - 14 April 2019, (Summary Text)

2019

73. Akut Flask Miyelit Tanili Olgularimizin Değerlendirilmesi

Edem P., Paketçi C., Soydemir D., Sarıkaya Uzan G., Bayram E., Hız A. S., et al.

5. Pediatrik Nöroimmünoloji Sempozyumu, Ankara, Turkey, 30 March 2019, pp.30, (Summary Text)

2019

74. Akut Flask Miyelit Tanili Olgularimizin Değerlendirilmesi

EDEM P., PAKETÇİ C., SOYDEMİR D., SARIKAYA UZAN G., BAYRAM E., HIZ KURUL S., et al.

5. Pediatrik Nöroimmünoloji Sempozyumu, Ankara, Turkey, 30 March 2019, (Summary Text)

2019

75. Çocukluk Çağı Başlangıçlı Multipl Skleroz

PAKETÇİ C., YİŞ U.

Dr. Behçet Uz Çocuk Kongresi, İzmir, Turkey, 28 February - 02 March 2019, vol.9, pp.35, (Summary Text)

2018

76. Children With Disabilities: Experiences From the Health Board of University Hospital

UĞUR BAYSAL S., İNCE O. T., YİŞ U., AYDIN A.

1st International Eurasian Congress of Social Pediatrics, İstanbul, Turkey, 28 November - 01 December 2018, (Summary Text)

2018

77. Glutaric Aciduria Type IIc: L377P Mutation Should Be Kept in Mind in Turkish Origine

TEKE KISA P., YİŞ U., cirak s., KÖSE E., ARSLAN N.

Society for the study of Inborn Error of Metabolism 2018, Atina, 04 September 2018, (Summary Text)

2018

78. Awereness and knowledge level of osteoporosis in patients with neuromuscular diseases- multicentre stduy

DİLEK B., ŞAHİN E., SERTPOYRAZ F., ERDİNÇ GÜNDÜZ N., DİKİCİ A., ENGİN O., et al.

13. Meeting of the Mediterranean Society of Myology, 27 - 29 June 2018, (Summary Text)

2018

79. Awareness and Knowledge Level of Osteoporosis in Patients with Neuromuscular Disease-Multicenter Study

DİLEK B., ŞAHİN E., SERTPOYRAZ F. M., ERDINC GUNDUZ N., DIKICI A., ENGIN O., et al.

13.Meeting of the Mediterranean Society of Myology ,2.Congress of the Turkish Neuromuscular Society, Nevşehir, Turkey, 27 - 29 June 2018, (Summary Text)

2018

80. Awereness and knowledge level of osteoporosis in patients with neuromuscular diseases- multicentre study

Dilek B., Şahin E., Sertpoyraz F. M., Erdinç Gündüz N., Dikici A., Engin O., et al.

13. Meeting of the Mediterranean Society of Myology, Nevşehir, Turkey, 27 June 2018, vol.37, pp.169, (Summary Text)

2018

81. NDUFA12 Gen Mutasyonu Saptanan İki Kardeşte Farklı Fenotipik Prezentasyon

YİŞ U., HIZ A. S., OKUR T. D., MANYAS H., PAKETÇİ C., BAYRAM E., et al.

20. Ulusal Çocuk Nörolojisi Kongresi, Cyprus (Kktc), 2 - 06 May 2018, pp.172, (Summary Text)

2018

82. Çocukluk Çağı Polinöropatileri: Dokuz Eylül Üniversitesi Çocuk Nörolojisi Deneyimi

PAKETÇİ C., MANYAS H., OKUR T. D., ÖZTURA İ., BAYDAN F., KARAKAYA M., et al.

20. Ulusal Çocuk Nörolojisi Kongresi, Cyprus (Kktc), 2 - 06 May 2018, pp.183, (Summary Text)

2018

83. Anti-NMDA Reseptör Ensefaliti

SÖNMEZ A., PAKETÇİ C., MANYAS H., OKUR D., BAYRAM E., YİŞ U., et al.

20. Ulusal Çocuk Nörolojisi Kongresi, Cyprus (Kktc), 2 - 06 May 2018, pp.129, (Summary Text)

2018

84. Çocuklarda Primer Başağrısı ile İlişkili Beyaz Cevher Lezyonlarının 2 Yıllık İzlem Sonuçları

BAYRAM E., YİŞ U., PAKETÇİ C., OKUR T. D., POLAT A. İ., ÇAKMAKÇI H., et al.

20. Ulusal Çocuk Nörolojisi Kongresi, Cyprus (Kktc), 2 - 06 May 2018, pp.135, (Summary Text)

2018

85. NDUFS3 Gen Mutasyonu İlişkili Atipik Bir Leigh Sendromu

HIZ A. S., YİŞ U., OKUR T. D., MANYAS H., PAKETÇİ C., BAYRAM E., et al.

20. Ulusal Çocuk Nörolojisi Kongresi, Cyprus (Kktc), 2 - 06 May 2018, pp.169, (Summary Text)

2018

86. HİPEROKSİK BEYİN HASARINDA MEMANTİNİN NÖROPROTEKTİF ETKİSİNİN ARAŞTIRILMASI

POLAT A. İ., CİLAKER MIÇILI S., ÇALIŞIR M., OKUR D., BAYRAM E., TUĞYAN K., et al.

20. Ulusal Çocuk Nörolojisi Kongresi, Cyprus (Kktc), 2 - 06 May 2018, vol.10, pp.81, (Summary Text)

2018

87. Rotavirüs İlişkili Ensefalopati ve Serebellit

PEKTANÇ M., PAKETÇİ C., MANYAS H., OKUR D., BAYRAM E., YİŞ U., et al.

20. Ulusal Çocuk Nörolojisi Kongresi, Cyprus (Kktc), 2 - 06 May 2018, pp.129, (Summary Text)

2018

88. Tip 1 diyabetli olguların sinir iletim çalışmalarının sonuçlarının değerlendirilmesi

AYANOĞLU M., YİŞ U., ÜNVER TUHAN H., POLAT A. İ., Okur D., EDEM P., et al.

20. Ulusal Çocuk Nöroloji kongresi, Turkey, 2 - 06 May 2018, (Summary Text)

2018

89. Tip 1 Diyabetli Olguların Sinir İletim Çalışmalarının Sonuçlarının Değerlendirilmesi

AYANOĞLU M., YİŞ U., ÜNVER TUHAN H., POLAT A. İ., OKUR T. D., EDEM P., et al.

20. Ulusal Çocuk Nörolojisi Kongresi, Cyprus (Kktc), 2 - 06 May 2018, pp.92, (Summary Text)

2017

90. KCNB1 MUTATIONS ARE CAUSING A NEURODEVELOPMENTAL DISORDER INCLUDING EPILEPSY AND AUTISM

Moller R. S., de Kovel C. G. F., Syrbe S., Schonewolf-Greulich B., Rokkjaer M., Svaneby D., et al.

32nd International Epilepsy Congress, Barcelona, Spain, 2 - 06 September 2017, vol.58, (Summary Text)

2017

91. Genetic Landscape of congenital myasthenic syndroms from Turkey: novel mutations and clinical insights

Yis U., Becker K., Kurul S., Uyanik G., Bayram E., Haliloglu G., et al.

22nd International Annual Congress of the World-Muscle-Society (WMS), Saint-Lo, France, 3 - 07 October 2017, vol.27, (Summary Text)

2017

92. Neronal Ceroid Lipofuscinosis :Two Families, Two forms, Two New Mutations

Yazıcı H., Canda E., Uçar S. K., POLAT M., YİŞ U., Aykut A., et al.

Journal of Inborn Errors of Metabolism and Screening, 5 - 08 September 2017, (Summary Text)

2017

93. Contribution of the Values of mean diffusion and anisotropic diffusion to diagnosis in patients with childhood absence epilepsy

BAYRAM E., ÇAYLAK H., ÖZTÜRK T., POLAT A. İ., YİŞ U., GÜLERYÜZ H., et al.

32nd INTERNATIONAL EPILEPSY CONGRESS, 2 - 06 September 2017, (Summary Text)

2017

94. Clinical characteristics and electroencephalographical evaluation of pediatric patients with autistic spectrum disorders

POLAT A. İ., HIZ A. S., YİŞ U., BAYRAM E., ayanoğlu m., OKUR T. D., et al.

32nd INTERNATIONAL EPILEPSY CONGRESS, 2 - 06 September 2017, (Summary Text)

2017

95. Neuronal ceroid lipofuscinosis: Twofamilies, two forms, two new mutations.

YAZICI H., CANDA E., KALKAN UÇAR S., POLAT M., YİŞ U., Aykut A., et al.

ICIEM 2017 13th International Congress of Inborn Errors of Metabolism, Brazil, 5 - 08 September 2017, vol.5, pp.342, (Summary Text)

2017

96. Nerve Conduction Studies in Type 1 Diabetes Mellitus

AYANOĞLU M., YİŞ U., ÜNVER TUHAN H., POLAT A. İ., OKUR T. D., EDEM P., et al.

12th European Paediatric Neurology Society (EPNS) Congress, Lyon, France, 20 - 24 June 2017, vol.21, pp.225, (Summary Text)

2017

97. Riboflavin Responsive Neuromusculary Disorders Broadphenotypic Spectrum and Importance of Genetic Analyses

POLAT İ., YİŞ U., ÇIRAK S., BECKER K., KARAKAYA M., ALTMÜLLER J., et al.

12th European Paediatric Neurology Society (EPNS) Congress, Lyon, France, 20 - 24 June 2017, vol.21, pp.156, (Summary Text)

2017

98. Nerve conduction study findings in children with cystic fibrosis

Polat I., YİŞ U., Köse S., Ayanoglu M., Okur D., Edem P., et al.

12th EPNS CONGRESS, 20 - 24 June 2017, vol.21, pp.228, (Summary Text)

2017

99. Anti-MOG positive pediatric cases with diverse clinical spectrum in demyelinating disorders

OKUR T. D., POLAT A. İ., KARAKAYA P., ÖZTÜRK T., AYANOĞLU M., EDEM P., et al.

12th EPNS CONGRESS, Lyon, France, 20 - 24 June 2017, (Summary Text)

2017

100. Nerve conduction study findings in children with cystic fibrosis

POLAT A. İ., YİŞ U., ŞİRİN KÖSE S., AYANOĞLU M., OKUR T. D., EDEM P., et al.

12th EPNS CONGRESS, Lyon, France, 20 - 24 June 2017, (Summary Text)

2017

101. Alternative medications for epilepsy of infancy with migrating focal seizures Potassium bromide and ketogenic diet

POLAT A. İ., AYANOĞLU M., OKUR T. D., EDEM P., PAKETÇİ C., BAYRAM E., et al.

12th EPNS CONGRESS, 20 - 24 June 2017, (Summary Text)

2017

102. Riboflavin responsive neuromusculary disorders broad phenotypic spectrum and importance of genetic analysis

POLAT A. İ., YİŞ U., sebahattin Ç., becker k., karakaya m., altmüller j., et al.

12th EPNS CONGRESS, 20 - 24 June 2017, (Summary Text)

2017

103. Alternative Medications for Epilepsy of Infancy with Migrating Focal Seizures; Potassium Bromide and Ketogenic Diet

POLAT A. İ., Ayanoglu M., Okur D., Edem P., PAKETÇİ C., BAYRAM E., et al.

12th European Paediatric Neurology Society (EPNS) Congress, Lyon, France, 20 - 24 June 2017, vol.21, pp.36-37, (Summary Text)

2017

104. Alternative medication for epilepsy of infancy with migrating focal seizures potassium bromide and ketogenic diet

POLAT A. İ., AYANOĞLU M., Okur D., YİŞ U., HIZ A. S.

12th EPNS Congress, Lyon, France, 20 - 24 June 2017, (Summary Text)

2017

105. Nöronal seroid lipofusinoz iki aile-iki form-iki yeni mutasyon

YAZICI H., CANDA E., KALKAN UÇAR S., POLAT M., YİŞ U., AYKUT A., et al.

XIV. Ulusal Metabolik Hastalıklar ve Beslenme Kongresi (Uluslararası Katılımlı)Bodrum, Turkey, 26 - 30 April 2017, (Summary Text)

2017

106. ESES tanılı olgularımızın değerlendirilmesi

EDEM P., BAYRAM E., AYANOĞLU M., POLAT A. İ., Okur D., PAKETÇİ C., et al.

19. Ulusal Çocuk Nöroloji Kongresi, Turkey, 19 - 23 April 2017, (Summary Text)

2017

107. İnfantil dönemde epileptik ensefalopati ile prezente olan bileşik heterozigot MTHFR mutasyonu saptanan bir olgu

AYANOĞLU M., YİŞ U., EDEM P., Okur D., POLAT A. İ., BAYRAM E., et al.

19. Ulusal Çocuk Nöroloji Kongresi, Turkey, 19 - 23 April 2017, (Summary Text)

2017

108. Ciddi difüzyon kısıtlılığı gözlenen bir LTBL olgusu

AYANOĞLU M., YİŞ U., GÜLERYÜZ H., POLAT A. İ., Karaoğlu P., Okur D., et al.

19. Ulusal Çocuk Nöroloji Kongresi, Turkey, 19 - 23 April 2017, (Summary Text)

2017

109. Herediter aksonal polinöropati tanısında yeni jenerasyon sekanslama tekniklerinin önemi

Okur D., YİŞ U., POLAT A. İ., Karakaya M., Altmüller J., Nürnberg P., et al.

19. Ulusal Çocuk Nöroloji Kongresi, Turkey, 19 - 23 April 2017, (Summary Text)

2017

110. İskemik inme olgularında epilepsi gelişimi açısından risk faktörlerinin tanımlanması

POLAT A. İ., AYANOĞLU M., Okur D., EDEM P., PAKETÇİ C., BAYRAM E., et al.

19. Ulusal Çocuk Nöroloji Kongresi, Turkey, 19 - 23 April 2017, (Summary Text)

2017

111. Ciddi Diffüzyon Kısıtlılığı Gözlenen Bir LTBL Olgusu

AYANOĞLU M., YİŞ U., GÜLERYÜZ UÇAR H., POLAT A. İ., KARAOĞLU P., OKUR T. D., et al.

19. Ulusal Çocuk Nörolojisi Kongresi, Antalya, Turkey, 19 - 23 April 2017, pp.192, (Summary Text)

2017

112. İnfantil Dönemde Epileptik Ensefalopati ile Prezente Olan Bileşik Heterozigot MTHFR Mutasyonu Saptanan Bir Olgu

AYANOĞLU M., YİŞ U., EDEM P., OKUR T. D., PAKETÇİ C., POLAT A. İ., et al.

19. Ulusal Çocuk Nörolojisi Kongresi, Antalya, Turkey, 19 - 23 April 2017, pp.191, (Summary Text)

2017

113. Antikoagülan ve/veya Antiplatelet Tercihlerinin İskemik İnme Seyrindeki Etkileri

POLAT A. İ., ÖZDENER M., AYANOĞLU M., OKUR T. D., EDEM P., PAKETÇİ C., et al.

19. Ulusal Çocuk Nörolojisi Kongresi, Antalya, Turkey, 19 - 23 April 2017, pp.163, (Summary Text)

2017

114. Antikoagulan ve/veya antiplatelet tercihlerinin iskemik inme seyrindeki etkileri

POLAT A. İ., Erdener M., AYANOĞLU M., Okur D., EDEM P., PAKETÇİ C., et al.

19. Ulusal Çocuk Nöroloji Kongresi, Turkey, 19 - 23 April 2017, (Summary Text)

2017

115. ESES Tanılı Olgularımızın Değerlendirilmesi

EDEM P., BAYRAM E., AYANOĞLU M., POLAT A. İ., OKUR D., PAKETÇİ C., et al.

19. Ulusal Çocuk Nörolojisi Kongresi, Antalya, Turkey, 19 - 23 April 2017, pp.113, (Summary Text)

2017

116. Streptococcus constellatus’a Bağlı Dissemine Enfeksiyon: Olgu Sunumu. 5-9 Nisan, 2017, Antalya

BELVERENLİ H., BELET N., ÖZLÜ C., Yiş U., GÜLERYÜZ H.

10. Ulusal Çocuk Enfeksiyon Hastalıkları Kongresi, Turkey, 5 - 09 April 2017, (Summary Text)

2016

117. Clinical, radiological, and genetic survey of patients with muscle eye brain disease caused by mutations in POMGNT1

Yis U., Uyamk G., Rosendahl D., ÇARMAN K. B., Bayram E., Heise M., et al.

21st International Congress of the World-Muscle-Society, Granada, Nicaragua, 4 - 08 October 2016, vol.26, (Summary Text)

2016

118. Nerve Conduction Studies in Children with Subclinical Hypothyroidism

ÇATLI G., YİŞ U., ÜNVER TUHAN H., AYANOĞLU M., HIZ A. S., BÖBER E., et al.

55rd Annual Meeting of the European Society for Paediatric Endocrinology (ESPE)., 10 - 12 September 2016, (Summary Text)

2016

119. Nadir görülen bir lipid depo hastalığı: Chanarin Dorfman Sendromu

AYANOĞLU M., KUYUM P., POLAT A. İ., OKUR T. D., YİŞ U., BAYRAM E., et al.

52. Türk Pediatri Kongresi, Turkey, 15 May 2016, (Summary Text)

2016

120. Nöropsikiyatrik ilaç kullanımı seyrinde karşılaşılan ilaç kesimini gerektiren yan etkiler ve olguların değerlendirilmesi

POLAT A. İ., AYANOĞLU M., OKUR T. D., BAYRAM E., YİŞ U., HIZ A. S.

52. Türk Pediatri Kongresi, Turkey, 16 May 2016, (Summary Text)

2016

121. Frontal lob epilepsisi için lokalize edici bir iktal fenomen “Chapeau de Gendarme

POLAT A. İ., AYANOĞLU M., Okur D., BAYRAM E., YİŞ U., HIZ A. S.

10. Ulusal Epilepsi Kongresi, Turkey, 12 - 15 May 2016, (Summary Text)

2016

122. West sendromu tanılı olguların klinik özelliklerinin değerlendirilmesi

POLAT A. İ., AYANOĞLU M., Okur D., BAYRAM E., YİŞ U., HIZ A. S.

10. Ulusal Epilepsi Kongresi, Turkey, 12 - 15 May 2016, (Summary Text)

2016

123. Serum pentraxin 3 levels in pediatric migraine patients

POLAT A. İ., ayanoğlu m., okur d., YİŞ U., HIZ A. S.

14th international child neurology congress, 1 - 05 May 2016, (Summary Text)

2016

124. Evaluation of autonomic dysfunction in pediatric migraine patients

Elitez D., YİŞ U., Demir N., ÖZTURA İ., POLAT A. İ., Ayanoğlu M., et al.

14th International Child Neurology Congress, 1 - 05 May 2016, (Full Text)

2016

125. Evaluation of Autonomic Dysfunction in pediatric migraine patients

elitez d., YİŞ U., demir n., ÖZTURA İ., POLAT A. İ., ayanoğlu m., et al.

14th international child neurology congress, 1 - 05 May 2016, (Summary Text)

2016

126. Pediatric multiple sclerosis MS is well studied clinically and radiologically but age related characteristics are not well described in early onset groups

öztürk z., KONUŞKAN B., CANPOLAT M., KUMANDAŞ S., KILIÇ B., DUMAN Ö., et al.

14th international child neurology congress, 1 - 05 May 2016, (Summary Text)

2016

127. Demyelinizan hastalık tanısı alan olgularımızın klinik, laboratuvar ve tedavi yanıtları yönünden değerlendirilmesi

OKUR T. D., POLAT A. İ., AYANOĞLU M., YİŞ U., BAYRAM E., HIZ A. S.

18. Ulusal çocuk nöroloji kongresi, Turkey, 20 April 2016, (Summary Text)

2016

128. Kistik fibrozis ile izlenen ve tedavi altındaki olgularda ENMG bulguları

POLAT A. İ., YİŞ U., AYANOĞLU M., OKUR T. D., BAYRAM E., HIZ A. S.

18. ulusal çocuk nöroloji kongresi, Turkey, 20 April 2016, (Summary Text)

2016

129. Otistik spektrum bozuklugu olgularında epilepsi gelişimi açısından risk faktörleri nelerdir

POLAT A. İ., HIZ A. S., YİŞ U., AYANOĞLU M., OKUR T. D., BAYRAM E., et al.

18. Ulusal Çocuk Nöroloji Kongresi, Turkey, 20 April 2016, (Summary Text)

2016

130. Anti-MOG antikor seropozitifliği saptanan farklı klinik karakterde demiyelizan hastalıklar

Okur D., POLAT A. İ., AYANOĞLU M., YİŞ U., BAYRAM E., HIZ A. S.

18. Ulusal Çocuk Nöroloji Kongresi, Turkey, 20 - 24 April 2016, (Summary Text)

2016

131. Çocuk Hematoloji ve Onkoloji Hastalarına yapılan ENMG sonuçlarının retrospektif olarak incelenmesi

AYANOĞLU M., YİŞ U., KIZMAZOĞLU D., POLAT A. İ., Okur D., BAYRAM E., et al.

18. Ulusal Çocuk Nöroloji Kongresi, Turkey, 20 - 24 April 2016, (Summary Text)

2016

132. Çocuk Acil servisten Çocuk Nöroloji Konsültasyonu istenen olguların değerlendirilmesi

POLAT A. İ., YİŞ U., AYANOĞLU M., Okur D., BAYRAM E., HIZ A. S.

18. Ulusal Çocuk Nöroloji Kongresi, Turkey, 20 - 24 April 2016, (Summary Text)

2016

133. Menkes Sendromu: ATP7A Mutasyonlu Nadir Bir Olgu

Gürsoy S., Ayanoğlu M., Köse E., Okur Altınyaprak D., Koç A., Giray Bozkaya Ö., et al.

3. Nörometabolik Dismorfoloji Sempozyumu, İstanbul, Turkey, 10 - 12 March 2016, pp.57, (Summary Text)

2015

134. Expression patterns of microRNAs 146A 34A 132 134 and in pediatric epilepsy patients

POLAT A. İ., Ayanoğlu M., Uğur T., GENÇ Ş., YİŞ U., HIZ A. S.

31. International Epilepsy Congress, 5 - 09 September 2015

2015

135. expression patterns of micrornas 146a 34a 132 184 in pediatric epilepsy patients

POLAT A. İ., müge a., kemal t., GENÇ Ş., YİŞ U., semra hız k.

31. international epilepsy congress, 5 - 09 September 2015, vol.56, pp.176, (Summary Text)

2015

136. effectiviness of methylprednisolone and diazepam for continous spike waves during slow wave sleep

POLAT A. İ., müge a., YİŞ U., semra hız k.

31 international epilepsy congress, 5 - 09 September 2015, vol.56, pp.176, (Summary Text)

2015

137. CLINICAL PREDICTORS OF INTRACTABLE EPILEPSY IN CHILDHOOD

Karaoğlu P., Yiş U., Polat İ., Ayanoğlu M., Hız A. S.

31st International Epilepsy Congress, İstanbul, Turkey, 5 - 09 September 2015, pp.98-99, (Summary Text)

2015

138. M.Pneumoniae ile ilişkili meningoensefalit ve transvers myelit olgusu

AYANOĞLU M., POLAT A. İ., Aykol D., Durmuş Yılmaz S., YİŞ U., HIZ A. S.

17. Ulusal Çocuk Nöroloji Kongresi, İzmir, Turkey, 06 June 2015, (Summary Text)

2015

139. Korpus kallozum Anormalliği Saptanan Olguların Klinik Bulgular ve Kromozomal Değişiklikler Açısından Değerlendirilmesi

BAYRAM E., Agilkaya S., Yasemin T., Pakize k., uluc y., CİNGÖZ S., et al.

16. Ulusal Çocuk Nörolojisi Kongresi, Turkey, 22 - 27 June 2015

2015

140. Ring Kromozom 20 Karyotipi Saptanan Olgu

Çankaya T., Ayanoğlu M., Bora E., Gürsoy S., Polat A. İ., Onur Cura D., et al.

17. Ulusal Çocuk Nöroloji Kongresi, İzmir, Turkey, 6 - 09 May 2015, pp.136, (Summary Text)

2015

141. Expression patterns of micro RNAs 146a 181a and 155 insubacute sclerosing panencephalitis

YİŞ U., uğur kemal t., GENÇ Ş., ÇARMAN K. B., BAYRAM E., yasemin t., et al.

11. European Pediatric Neurology Congress, 27 - 30 May 2015, vol.19, pp.27, (Summary Text)

2015

142. Simvastatin alleviates cell death and apoptosis in the developing brain of rat after pentylenetetrazole induced status epilepticus

yasemin t., BAYRAM E., ÖZBAL S., YİŞ U., TUĞYAN K., pakize k., et al.

11. european pediatric neurology congress, Turkey, 27 - 30 May 2015, (Summary Text)

2015

143. Expression patterns of microRNAs 146A 181A and 155 in subacute sclerosing panencephalitis

YİŞ U., Uğur T., GENÇ Ş., Çarman B., BAYRAM E., Yasemin T., et al.

11. European Pediatric Neurology Society Congress, 27 - 30 May 2015

2015

144. Simvastatin alleviates cell detah and apoptosis in the developing brain of rat after pentylenetetrazole induced status epilepticus

TOPÇU Y., BAYRAM E., ÖZBAL S., YİŞ U., TUĞYAN K., KARAOĞLU P., et al.

11th EPNS Congress, 27 - 30 May 2015, vol.19, pp.56

2015

145. Çocukluk çağında dirençli epilepsi gelişimini öngören faktörler

KARAOĞLU P., YİŞ U., POLAT A. İ., AYANOĞLU M., HIZ A. S.

17. Ulusal Çocuk Nörolojisi Kongresi, İzmir, Turkey, 06 May 2015, pp.46, (Summary Text)

2015

146. Miyastenia Gravis nedeniyle takip edilen vakalarımızın değerlendirilmesi

YİŞ U., KARAOĞLU P., POLAT A. İ., AYANOĞLU M., YILMAZ Ü., TOSUN A., et al.

17. Ulusal Çocuk Nörolojisi Kongresi, İzmir, Turkey, 06 May 2015, pp.86, (Summary Text)

2015

147. MowatWilson sendromlu bir olgu

Polat A. İ., Gürsoy S., Ayanoğlu M., Yiş U., Giray Bozkaya Ö., Ataman E., et al.

17. Ulusal Çocuk Nöroloji Kongresi, İzmir, Turkey, 6 - 09 May 2015, pp.137, (Summary Text)

2015

148. Çok uzun zincirli Açil KoA dehidrogenaz eksikliği saptanan bir olgu

AYANOĞLU M., POLAT A. İ., KARAOĞLU P., YİŞ U., HIZ A. S.

17. Ulusal Çocuk Nörolojisi Kongresi, İzmir, Turkey, 06 May 2015, pp.142, (Summary Text)

2019

149. Ailesel Akdeniz Ateşi ile ilişkili uzamış miyalji ve akut duysal motor aksonal polinöropati: 2 olgu

YİŞ U., AYANOĞLU M., POLAT A. İ., HIZ A. S.

17. Ulusal Çocuk Nöroloji Kongresi, Turkey, 06 May 2019 - 09 May 2015, (Summary Text)

2015

150. Mikrosefali kapiller malformasyon sendromu

pakize k., POLAT A. İ., müge a., YİŞ U., semra hız k.

17. ulusal çocuk nöroloji kongresi, Turkey, 6 - 09 May 2015, (Summary Text)

2015

151. Solunum sıkıntısı geliştiren ailesel hipokalemik periyodik paralizi olgusu

POLAT A. İ., AYANOĞLU M., YİŞ U., HIZ A. S.

17. Ulusal Çocuk Nöroloji Kongresi, Turkey, 6 - 09 May 2015, (Summary Text)

2015

152. Çocukluk çağı epilepsi olgularında MikroRNA 146a, 34a, 132, 134, 184 ekspresyonu

POLAT A. İ., AYANOĞLU M., YİŞ U., HIZ A. S.

17. Ulusal Çocuk Nöroloji Kongresi, Turkey, 6 - 09 May 2015, (Summary Text)

2015

153. megakonial konjenital musküler disrofi

YİŞ U., figen b., müge a., POLAT A. İ., semra hız k.

17. ulusal çocuk nöroloji kongresi, Turkey, 6 - 09 May 2015, (Summary Text)

2015

154. Tek merkezde çocukluk çağı inme olgularının değerlendirlmesi ve altı aylık izlem sonuçları

POLAT A. İ., AYANOĞLU M., YİŞ U., HIZ A. S.

17. Ulusal Çocuk Nöroloji Kongresi, Turkey, 6 - 09 May 2015, (Summary Text)

2015

155. Ender bir fakomatoz olgusu: Nörokutanöz Melanozis

YİŞ U., AYANOĞLU M., POLAT A. İ., GÜLERYÜZ H., HIZ A. S.

17. Ulusal Çocuk Nöroloji Kongresi, Turkey, 6 - 09 May 2015, (Summary Text)

2015

156. Epileptik nistagmus, vizüel, vertigo ve jelastik nöbetleri olan bir olgu

AYANOĞLU M., POLAT A. İ., YİŞ U., HIZ A. S.

17. Ulusal Çocuk Nöroloji Kongresi, Turkey, 06 May 2015 - 09 May 2019, (Summary Text)

2015

157. Megakonial Konjenital Muskuler Distrofi

YİŞ U., Baydan F., AYANOĞLU M., POLAT A. İ., HIZ A. S., Çırak S.

17. Ulusal Çocuk Nöroloji Kongresi, Turkey, 6 - 09 May 2015, (Summary Text)

2015

158. Aminotransferaz Yüksekliğinin Karaciğer Dışı Nedeni- Musküler Distrofi: Olgu Sunumu

Erbağcı O., Kuyum P., Aksoy B., Altekin E., Ayanoğlu M., Yiş U., et al.

XV. Ulusal Klinik Biyokimya Kongresi, Muğla, Turkey, 23 - 26 April 2015, pp.20-21, (Summary Text)

2015

159. intrakraniyal enfeksiyonlar

YİŞ U.

16. DEÜTF Pediatri Günleri, Turkey, 12 - 13 March 2015

2015

160. EFFECTIVENESS OF METHYLPREDNISOLONE AND DIAZEPAM FOR CONTINUOUS SPIKE WAVES DURING SLOW WAVE SLEEP

Polat I., Ayanoglu M., Yis U., Kurul S. H.

31st International Epilepsy Congress, İstanbul, Turkey, 5 - 09 September 2015, vol.56, pp.176, (Summary Text)

2015

161. EXPRESSION PATTERNS OF MICRORNAS-146A,-34A,-132,-134 AND-184 IN PEDIATRIC EPILEPSY PATIENTS

Polat I., Ayanoglu M., Tufekci U., GENÇ Ş., Yis U., Kurul S. H.

31st International Epilepsy Congress, İstanbul, Turkey, 5 - 09 September 2015, vol.56, pp.176, (Summary Text)

2015

162. CLINICAL PREDICTORS OF INTRACTABLE EPILEPSY IN CHILDHOOD

Karaoglu P., Yis U., Polat A. I., Ayanoglu M., HIZ A. S.

31st International Epilepsy Congress, İstanbul, Turkey, 5 - 09 September 2015, vol.56, pp.98-99, (Summary Text)

2014

163. Intravenous Levetiracetam for Treatment of Seizures in Term and Preterm Neonates

KARAOĞLU P., HIZ A. S., İŞCAN B., POLAT A. İ., AYANOĞLU M., DUMAN N., et al.

The16th Annual Meeting of Infantile Seizure SocietyISES 2014, Nevşehir, Turkey, 22 June 2014, (Summary Text)

2014

164. Çocukluk çağı dirençli epilepsi olgularında D vitamini düzeyinin değerlendirilmesi

KARAOĞLU P., POLAT A. İ., AYANOĞLU M., YİŞ U., HIZ A. S.

16. Ulusal Çocuk Nörolojisi Kongresi, Nevşehir, Turkey, 22 June 2014, pp.26, (Summary Text)

2014

165. Inflammation and anemia in simple febrile seizures and complex febrile seizures

POLAT A. İ., KARAOĞLU P., AYANOĞLU M., YİŞ U., HIZ A. S.

The 16th Annual Meeting of the Infantile Seizure Society ISES 2014 (Joint Meeting of the Infantile Seizure Society and the Turkish Child Neurology Association), Nevşehir, Turkey, 22 June 2014, pp.35-36, (Summary Text)

2014

166. Spinocerebellar ataxia type 2 with electrical status epilepticus during slow-wave sleep (ESES)

POLAT A. İ., KARAOĞLU P., AYANOĞLU M., ÖZTÜRK T., YİŞ U., GÜLERYÜZ UÇAR H., et al.

The 16th Annual Meeting of the Infantile Seizure Society ISES 2014 (Joint Meeting of the Infantile Seizure Society and the Turkish Child Neurology Association), Nevşehir, Turkey, 22 June 2014, pp.72, (Summary Text)

2014

167. Görme bulanıklığı ve baş ağrısı bulguları olan bir olgu; Vogt-Koyanagi-Harada sendromu

POLAT A. İ., KARAOĞLU P., AYANOĞLU M., ÇATAL E., TAKEŞ Ö., YİŞ U., et al.

16. Ulusal Çocuk Nörolojisi Kongresi, Nevşehir, Turkey, 22 June 2014, pp.182, (Summary Text)

2014

168. Nadir bir paraenfeksiyöz patoloji; akut hemiserebellit

POLAT A. İ., KARAOĞLU P., AYANOĞLU M., ÖZTÜRK T., YİŞ U., GÜLERYÜZ UÇAR H., et al.

16. Ulusal Çocuk Nörolojisi Kongresi, Nevşehir, Turkey, 22 June 2014, pp.183, (Summary Text)

2014

169. Subakut sklerozan panensefalitli hastalarda mikroRNA 146a, 181a ve 155'in ekspresyon paterninin belirlenmesi

YİŞ U., TÜFEKÇİ U., GENÇ Ş., ÇARMAN K. B., TOPÇU Y., BAYRAM E., et al.

16. Ulusal Çocuk Nörolojisi Kongresi, Nevşehir, Turkey, 22 June 2014, pp.116, (Summary Text)

2014

170. Kas katılığı ve myopati nedeni olarak Schwartz Jampel sendromlu bir olgu

POLAT A. İ., KARAOĞLU P., AYANOĞLU M., ÖZTÜRK T., YİŞ U., GÜLERYÜZ UÇAR H., et al.

16. Ulusal Çocuk Nörolojisi Kongresi, Nevşehir, Turkey, 22 June 2014, pp.183, (Summary Text)

2014

171. Selenoprotein N1 ilişkili miyopati ve riboflavin tedavisi

KARAOĞLU P., POLAT A. İ., AYANOĞLU M., YİŞ U., ÇIRAK S., HIZ A. S.

16. Ulusal Çocuk Nörolojisi Kongresi, Nevşehir, Turkey, 22 June 2014, pp.151-152, (Summary Text)

2014

172. Dropped head konjenital musküler distrofi

KARAOĞLU P., POLAT A. İ., AYANOĞLU M., YİŞ U., ÇIRAK S., HIZ A. S.

16. Ulusal Çocuk Nörolojisi Kongresi, Nevşehir, Turkey, 22 June 2014, pp.151, (Summary Text)

2014

173. Schimke immunoosseoz displazi tanısında nörolojik ve kutanöz bulguların önemi

POLAT A. İ., KARAOĞLU P., AYANOĞLU M., ÖZTÜRK T., YİŞ U., GÜLERYÜZ UÇAR H., et al.

16. Ulusal Çocuk Nörolojisi Kongresi, Nevşehir, Turkey, 22 June 2014, pp.182, (Summary Text)

2014

174. Intravenous levetiracetam for the treatment of seizures in term and preterm neonates

KARAOĞLU P., HIZ A. S., İŞCAN B., POLAT A. İ., AYANOĞLU M., DUMAN N., et al.

The 16th Annual Meeting of the Infantile Seizure Society ISES 2014 (Joint Meeting of the Infantile Seizure Society and the Turkish Child Neurology Association), Nevşehir, Turkey, 22 June 2014, pp.49, (Summary Text)

2014

175. Radyolojik izole sendromlu adolesan olgu: multiple skleroz için risk faktörleri

UĞUZ H., POLAT A. İ., KARAOĞLU P., AYANOĞLU M., YİŞ U., HIZ A. S.

3. Pediatri Uzmanlık Akademisi Kongresi, Turkey, 30 April 2014, (Summary Text)

2014

176. Mycoplasma Pneumoniae enfeksiyonu ilişkili anti-gangliosidantikorlarının negatif olduğu Fisher-Bickerstaff sendromu olgu sunumu

YİŞ U., KARAOĞLU P., POLAT A. İ., AYANOĞLU M., GÜLERYÜZ UÇAR H., HIZ A. S.

3. Pediatri Uzmanlık Akademisi Kongresi, Turkey, 30 April - 04 May 2014, (Summary Text)

2014

177. Mycoplasma Pneumoniae enfeksiyonu ile ilişkili geçici striatal tutulum görülen, sık nöbet geçiren ve hızlı iyileşme gösteren bir olgu

YİŞ U., KARAOĞLU P., POLAT A. İ., GÜLERYÜZ UÇAR H., HIZ A. S.

3. Pediatri Uzmanlık Akademisi Kongresi, Antalya, Turkey, 30 April 2014, pp.100-101, (Summary Text)

2014

178. Mycoplasma pneumoniae enfeksiyonu ile ilişkili geçisi striaal tutulum görülen, sık nöbet geçiren ve hızlı iyileşme gösteren bir olgu

YİŞ U., KARAOĞLU P., POLAT A. İ., GÜLERYÜZ UÇAR H., HIZ A. S.

3. Pediatri uzmanlık akademisi kongresi, Turkey, 30 April 2014, (Summary Text)

2014

179. Mycoplasma Pneumoniae enfeksiyonu ile ilişkili, antigangliosid antikorların negatif olduğu Fisher-Bickerstaff sendromu-olgu sunumu

YİŞ U., KARAOĞLU P., POLAT A. İ., AYANOĞLU M., GÜLERYÜZ UÇAR H., HIZ A. S.

3. Pediatri Uzmanlık Akademisi Kongresi, Antalya, Turkey, 30 April 2014, pp.101-102, (Summary Text)

2014

180. Radyolojik izole sendromlu adölesan olgu: multipl skleroz için risk faktörleri

UĞUZ H., POLAT A. İ., KARAOĞLU P., AYANOĞLU M., YİŞ U., HIZ A. S.

3. Pediatri Uzmanlık Akademisi Kongresi, Antalya, Turkey, 30 April 2014, pp.110, (Summary Text)

2014

181. Mukopolisakkaridoz Ti3B: Uzun Süreli Nörolojik İzlem”

HIZ A. S., YİŞ U., Karaoğlu P., POLAT A. İ., AYANOĞLU M.

4th Uluslararası Katılımlı Lizozomal Hastalıklar Kongresi, 17 - 20 April 2014, (Summary Text)

2014

182. Travma sonrası kronik spinal epidural hematom gelişen pediatrik olgu

KALEMCİ O., UR K., AKYOLDAŞ G., YİŞ U., ÖZTURA İ., GÜLERYÜZ H., et al.

Türk Nöroşirurji Derneği 28. Bilimsel Kongresi, Antalya, Turkey, 4 - 08 April 2014, vol.24, pp.192

2013

183. Caffeic acid phenethyl ester blocks cell death and apoptosis in the developing brain after pentylenetetrazole induced status epilepticus

YİŞ U., TOPÇU Y., ÖZBAL S., TUĞYAN K., BAYRAM E., KARAOĞLU P., et al.

10the EPNS congress, 25 - 28 September 2013

2013

184. The efficacy and safety of levetiracetam in pediatric patients treated with chemotherapeutic agents for hematologic disorders

BAYRAM E., TOPÇU Y., TÜFEKÇİ Ö., KARAOĞLU P., YİŞ U., ÖREN H., et al.

10th European Pediatric Neurology Society (EPNS) Congress, Brüksel, Belgium, 25 September 2013, pp.76, (Summary Text)

2013

185. Caffeic acid phenethyl ester blocks cell death and apoptosis in the developing brain of rat after pentylenetetrazole induced status epilepticus

YİŞ U., TOPÇU Y., ÖZBAL S., TUĞYAN K., BAYRAM E., KARAOĞLU P., et al.

10th European Pediatric Neurology Society (EPNS) Congress, Brüksel, Belgium, 25 September 2013, pp.114, (Summary Text)

2013

186. Incidental white matter lesions in children presenting with headache

BAYRAM E., TOPÇU Y., KARAOĞLU P., YİŞ U., GÜLERYÜZ UÇAR H., HIZ A. S.

10th European Pediatric Neurology Society (EPNS) Congress, Brüksel, Belgium, 25 September 2013, pp.17-18, (Summary Text)

2013

187. EVALUATION OF THE EFFECTS OF HYPERGLYCEMIA ON DEVELOPING BRAIN IN PRETERM NEONATES

Tayman C., Yis U., Hirfanoglu I., Oztekin O., Goektas G., Bilgin B. C.

24th Annual Meeting of the European-Society-of-Paediatric-and-Neonatal-Intensive-Care, Rotterdam, Netherlands, 12 - 15 June 2013, vol.39, (Summary Text)

2013

188. Defektif distroglikan glikozilasyonu ve kollajen VI eksikliği tanıları ile takip edilen konjenital musküler distrofili hastalarımızın değerlendirilmesi

YİŞ U., UYANIK G., ROSENDAHL D. M., ÇIRAK S., KARAOĞLU P., ÇARMAN K. B., et al.

15. Ulusal Çocuk Nörolojisi Kongresi, Sivas, Turkey, 22 May 2013, pp.60, (Summary Text)

2013

189. Lipid metabolizma bozukluğuna bağlı rekürren rabdomiyoliz: iki olgu sunumu

TOPÇU Y., KARAOĞLU P., BAYRAM E., YİŞ U., HIZ A. S.

15. Ulusal Çocuk Nörolojisi Kongresi, Sivas, Turkey, 22 May 2013, pp.125-126, (Summary Text)

2013

190. Yenidoğan Sıçanlarda Hiperoksik Beyin Hasarında Zonisamid Tedavisinin Nöroprotektif Etkilerinin Değerlendirilmesi

TOPÇU Y., BAYRAM E., ÖZBAL S., YİŞ U., TUĞYAN K., KARAOĞLU P., et al.

XV. Ulusal Çocuk Nörolojisi Kongresi, Turkey, 22 - 25 May 2013

2013

191. Pentilentetrazol ile oluşturulmuş status epileptikus modelinde gelişen beyinde kafeik asit fenetil esterin nöroprotektif etkinliğinin araştırılması

YİŞ U., TOPÇU Y., ÖZBAL S., TUĞYAN K., BAYRAM E., KARAOĞLU P., et al.

15. Ulusal Çocuk Nörolojisi Kongresi, Sivas, Turkey, 22 May 2013, pp.81, (Summary Text)

2013

192. Degos Hastalığına Bağlı Nörolojik Tutulum-Olgu Sunumu

KARAOĞLU P., TOPÇU Y., BAYRAM E., YİŞ U., AKARSU S., ATALAY E., et al.

15. Ulusal Çocuk Nörolojisi Kongresi, Sivas, Turkey, 22 May 2013, pp.109, (Summary Text)

2013

193. DEÜ çocuk nöroloji polikliniğine son bir yılda başvuran pediatrik multipl skleroz olgularının değerlendirilmesi

KARAOĞLU P., TOPÇU Y., BAYRAM E., YİŞ U., HIZ A. S.

15. Ulusal Çocuk Nörolojisi Kongresi, Sivas, Turkey, 22 May 2013, (Summary Text)

2013

194. Çocukluk döneminde pentilentetrazol ile oluşturulan deneysel status epileptikus modelinde simvastatinin nöroprotektif etkinliğinin araştırılması

TOPÇU Y., BAYRAM E., ÖZBAL S., YİŞ U., TUĞYAN K., KARAOĞLU P., et al.

15. Ulusal Çocuk Nörolojisi Kongresi, Sivas, Turkey, 22 May 2013, pp.125, (Summary Text)

2013

195. Çocukluk Döneminde Pentilentetrazol ile Oluşturulan Deneysel Status Modelinde Simvastatinin Nöroprotektif Etkinliğinin Araştırılması

TOPÇU Y., BAYRAM E., ÖZBAL S., YİŞ U., TUĞYAN K., KARAOĞLU P., et al.

XV. Ulusal Çocuk Nörolojisi Kongresi, Turkey, 22 - 25 May 2013

2013

196. Pentilentetrazol ile Oluşturrulmuş Status Epileptikus Modelinde Gelişen Beyinde Kafeik Asit Fenetil Esterin Nöroprotektif Etkinliğinin Araştırılması

YİŞ U., TOPÇU Y., ÖZBAL S., TUĞYAN K., BAYRAM E., KARAOĞLU P., et al.

XV. Ulusal Çocuk Nörolojisi Kongresi, Turkey, 22 - 25 May 2013

2013

197. Yaygın Kortikal Displazili Bir Olgu

Çakmaklı S., ÇANKAYA T., Aksel Kılıçaslan Ö., Karaoğlu P., ONUR CURA D., YİŞ U., et al.

2. Nörometabolik Dismorfoloji Sempozyumu, Turkey, 8 - 09 March 2013, (Summary Text)

2013

198. Yaygın kortikal displazili olgu

ÇAKMAKLI S., ÇANKAYA T., AKSEL Ö., KARAOĞLU P., ONUR CURA D., YİŞ U., et al.

2. Nörometabolik Dismorfoloji Sempozyumu, İstanbul, Turkey, 08 March 2013, pp.22, (Summary Text)

2012

199. Nöbetle başvuran bir Ito Hipomelanozis olgusu

HIZ A. S., TOPÇU Y., BAYRAM E., KARAOĞLU P., YİŞ U.

8. Ulusal Epilepsi Kongresi, Muğla, Turkey, 24 May 2012, pp.54-55, (Summary Text)

2012

200. An infant with recurrent benign sixth nerve palsy

KARAOĞLU P., TOPÇU Y., BAYRAM E., YİŞ U., HIZ A. S.

24th Annual Meeting of European Academy of Childhood Disability, Joint of 14th National Pediatric Neurology Congress, İstanbul, Turkey, 16 May 2012, pp.149, (Summary Text)

2012

201. A rare disorder: Goltz Gorlin syndrome

KARAOĞLU P., BAYRAM E., TOPÇU Y., YİŞ U., HIZ A. S.

24th Annual Meeting of European Academy of Childhood Disability, Joint of 14th National Pediatric Neurology Congress, İstanbul, Turkey, 16 May 2012, pp.169, (Summary Text)

2012

202. Coexistence of myositis, transverse myelitis, and Guillain Barre syndrome following Mycoplasma pneumoniae infection

TOPÇU Y., BAYRAM E., KARAOĞLU P., YİŞ U., GÜLERYÜZ UÇAR H., HIZ A. S.

24th Annual Meeting of European Academy of Childhood Disability, Joint of 14th National Pediatric Neurology Congress, İstanbul, Turkey, 16 May 2012, pp.69, (Summary Text)

2022

203. Correlation Between Expanded Hammersmith Functional Motor Scale, Body Composition and Anthropometry in Patients with Duchenne Muscular Dystrophy

Bayram E., Şahin E., Karaoğlu P., Topçu Y., Torun Bayram M., Erdinç Gündüz N., et al.

24th Annual Meeting of European Academy of Childhood Disability, İstanbul, Turkey, 16 May 2022, pp.142, (Summary Text)

2012

204. Evaluation of serum lipids and carotid artery intima media thickness in children and adolescents with Duchenne muscular dystrophy

TOPÇU Y., BAYRAM E., KARAOĞLU P., UZ G., GÜLERYÜZ UÇAR H., YİŞ U., et al.

24th Annual Meeting of European Academy of Childhood Disability, Joint of 14th National Pediatric Neurology Congress, İstanbul, Turkey, 16 May 2012, pp.144, (Summary Text)

2012

205. Evaluation of epicardial adipose tissue and carotid intima-media thicknesses in children with migraine

TOPÇU Y., BAYRAM E., KARAOĞLU P., KIR M., UZ G., GÜLERYÜZ UÇAR H., et al.

24th Annual Meeting of European Academy of Childhood Disability, Joint of 14th National Pediatric Neurology Congress, İstanbul, Turkey, 16 May 2012, pp.177, (Summary Text)

2012

206. Myopathic changes in muscle biopsy of a case with infantile systemic hyalinosis

BAYRAM E., TOPÇU Y., KARAOĞLU P., FIRAT C., YİŞ U., ÖZER E., et al.

24th Annual Meeting of European Academy of Childhood Disability, Joint of 14th National Pediatric Neurology Congress, İstanbul, Turkey, 16 May 2012, pp.142, (Summary Text)

2012

207. Sleep disturbance in children with cerebral palsy

KARAOĞLU P., TOPÇU Y., BAYRAM E., YİŞ U., HIZ A. S.

24th Annual Meeting of European Academy of Childhood Disability, Joint of 14th National Pediatric Neurology Congress, İstanbul, Turkey, 16 May 2012, pp.103, (Summary Text)

2012

208. Clinical correlation between body composition and motor limitations in patients with cerebral palsy

BAYRAM E., TOPÇU Y., KARAOĞLU P., TORUN BAYRAM M., ŞAHİN E., YİŞ U., et al.

24th Annual Meeting of European Academy of Childhood Disability, Joint of 14th National Pediatric Neurology Congress, İstanbul, Turkey, 16 May 2012, pp.101, (Summary Text)

2012

209. Rotavirüs gastroenteriti ile ilişkili benign afebril konvülziyonlu olguların değerlendirilmesi

TOPÇU Y., BAYRAM E., KARAOĞLU P., YİŞ U., HIZ A. S.

1. Pediatri Uzmanlık Akademisi Kongresi, Antalya, Turkey, 23 April 2012, pp.191, (Summary Text)

2010

210. Amphiphysin 2 (BIN1) and triad defects in several forms of centronuclear myopathies

Toussaint A., Maurer M., Cowling B. S., Hnia K., Mohr M., Oldfors A., et al.

15th International Congress of the World-Muscle-Society, Kumamoto, Japan, 12 - 16 October 2010, vol.20, pp.611, (Summary Text)

2010

211. NEUROPROTECTIVE EFFECTS OF RECOMBINANT HUMAN ERYTHROPOIETIN IN THE DEVELOPING BRAIN OF RAT AFTER LITHIUM-PILOCARPIN INDUCED STATUS EPILEPTICUS

Kurul H. S., Sozmen C. S., Yis U., Tugyan K., Baykara B., Yilmaz O.

9th European Congress on Epileptology, Rhodes, Greece, 27 June - 01 July 2010, vol.51, pp.83, (Summary Text)

2008

212. THE RELATIONSHIP OF NEONATAL SUBCLINICAL ELECTROGRAPHIC SEIZURES TO NEURODEVELOPMENTAL OUTCOME AT ONE YEAR OF AGE

Kurul S. H., Sutcuoglu S., Yis U., Duman N., Kumral A., ÖZKAN H.

8th European Congress on Epileptology, Berlin, Germany, 21 - 25 September 2008, vol.50, pp.240, (Summary Text)

2008

213. Chronic inflammatory demyelinating polyneuropathy in an eight year old girl

Kurul S. H., Yis U., Senocak O.

International Conference on Diagnosis and Treatment in Pediatric Neurology, Warszawa, Poland, 14 - 17 May 2008, pp.45-46, (Full Text)

2007

214. Hyperoxia causes cell death in the hippocampus of the developing brain

HIZ KURUL S., YİŞ U., KUMRAL A., CİLAKER MIÇILI S., TUĞYAN K., GENÇ Ş., et al.

7th Paediatric Neurology Society (EPNS) Congress, Kuşadası, Turkey, 26 - 29 September 2007, vol.11, pp.52, (Full Text)

2007

215. Hyperoxia causes cell death in the prefrontal cortex of the developing brain

YİŞ U., HIZ KURUL S., KUMRAL A., CİLAKER MIÇILI S., TUĞYAN K., GENÇ Ş., et al.

7th Paediatric Neurology Society (EPNS) Congress, Kuşadası, Turkey, 26 - 29 September 2007, vol.11, pp.53, (Full Text)

2006

216. Walker-Warburg syndrome: case report

Yis U., Kurul S., Uyanik G., Dirik E.

11th International Congress on Neuromuscular Diseases, İstanbul, Turkey, 2 - 07 July 2006, vol.16, (Summary Text)

2005

217. Assessment of urinary and serum cystatin C in determination of renal function in children with renal scar

Islekel H., Yis U., ALTUN Z. S., Soylu A., Turkmen M., Kavukcu S.

IUBMB 50th Anniversary Symposium, Budapest, Hungary, 2 - 07 July 2005, vol.272, pp.495, (Summary Text)

2014

218. Pediatrik beyin sapı lezyonlarında MRG ile ayırıcı tanı nasıl yapılır?

Öztürk Atasoy T., BARIŞ M. M., GÜLERYÜZ H., POLAT A. İ., YİŞ U.

TÜRKRAD 2014, Turkey, 11 - 16 November 2014, (Summary Text)

Books

2025

1. Arthrogryposis

Polat A. İ., Yiş U., Topaloğlu H.

in: Encyclopedia of the Neurological Sciences, John D. England, Editor, Academic Press , Massachusetts, pp.43-71, 2025

2025

2. Multipl Sklerozun Patogenezi

Şenol H. B., Yiş U.

in: Pediatrik Multipl Skleroz, Mehmet Canpolat, Editor, Akademisyen Yayınevi Kitabevi, Ankara, pp.27-35, 2025

2025

3. Spinal Muscular Atrophy Drug Treatment Methods

Sönmezoğlu D., Yiş U.

in: Spinal Muskuler Atrofi, Prof.Dr. Kürşat Bora Çarman, Editor, Türkiye Klinikleri Yayınevi, Ankara, pp.59-64, 2025

2025

4. acquired disorders of the neuromuscular junction

topaloğlu h., YİŞ U.

in: Swaiman's pediatric neurology, ashwall stephan, pearl philip L., Editor, Elsevier, philedelphia, pp.1440-1148, 2025

2024

5. Diagnosis Methods of Metabolic Myopathies: Electrophysiological Evaluation (Electromyography and Nerve Conduction Studies)

Şenol H. B., Günay Ç., Yiş U.

in: Inherited Metabolic Myopathies, Prof. Dr. İlyas OKUR, Editor, Türkiye Klinikleri Yayınevi, Ankara, pp.71-76, 2024

2023

6. Congenital myopathies

Yiş U., Polat A. İ., Diniz G.

in: Clues for Differential Diagnosis of Neuromuscular Disorders, Diniz G., Editor, Springer Nature, Aarau, pp.219-248, 2023

2023

7. Musküler Distrofilerde Genetik Yaklaşım

Günay Ç., Yiş U., Per H.

in: Çocuk Nörolojisinde Genetik Yaklaşımlar, Ayşe Semra Hız,Sarenur Gökben, Editor, Türkiye Klinikleri Yayınevi, Ankara, pp.72-77, 2023

2023

8. Konjenital miyopatiler

soydemir d., YİŞ U.

in: Temel Pediatrik Nöroloji: Tanı ve Tedavi, Kumandaş Sefer, Canpolat Mehmet, Editor, Akademisyen, pp.3109-3128, 2023

2023

9. Yoğun bakım hastalarında Devamlı EEG monitorizasyon ve EEG bulguları

Aykol D., Üstebay D. Ü., Yiş U.

in: Pediatrik ve Neonatal EEG Atlası, SEFER KUMANDAŞ,MEHMET CANPOLAT, Editor, Akademisyen Yayınevi Kitabevi, Ankara, pp.120-130, 2023

2022

10. CK YÜKSEKLIĞINE TANISAL YAKLAŞIM- ALGORITMA

Sarıkaya Uzan G., Yiş U.

in: Pediatrik Nöroloji Algoritmalar ve İlaç Rehberi, Sefer Kumandaş,Mehmet Canpolat, Editor, Akademisyen Kitabevi, İstanbul, pp.423-425, 2022

2022

11. "Konjenital Miyopatiler"

Soydemir D., Yiş U.

in: "Temel Pediatrik Nöroloji: Tanı ve Tedavi", Sefer Kumandaş,Mehmet Canpolat, Editor, Akademisyen Yayınevi Kitabevi, Ankara, pp.3109-3128, 2022

2022

12. KREATİN KİNAZ YÜKSEKLİĞİNE TANISAL YAKLAŞIM

Sarıkaya Uzan G., Yiş U.

in: TEMEL PEDİATRİK NÖROLOJİ: TANI VE TEDAVİ, Sefer Kumandaş,Mehmet Canpolat, Editor, Akademisyen Yayınevi Kitabevi, İstanbul, pp.3059-3069, 2022

2022

13. Pediatrik Nöromusküler Hastalıklarda Tanı ve Tedavi Algoritması

Polat A. İ., Yiş U.

in: Pediatrik Nöroloji: Algoritmalar ve İlaç Rehberi, Kumandaş S.,Canpolat M., Editor, Akademisyen Kitabevi, Ankara, pp.485-496, 2022

2022

14. Juvenil Miyastenia Gravis Olgularında Tanı ve Tedaviye Yaklaşım Algoritmaları

Özsoy Ö., Yiş U.

in: Pediatrik Nöroloji Algoritmalar ve İlaç Rehberi, Sefer Kumandaş,Mehmet Canpolat, Editor, Akademisyen Kitabevi, Ankara, pp.535-538, 2022

2022

15. Konjenital Miyopatilerde Tanısal Algoritmik Yaklaşım

Soydemir D., Yiş U.

in: Pediatrik Nöroloji Algoritmalar ve İlaç Rehberi, Sefer Kumandaş,Mehmet Canpolat, Editor, Akademisyen Yayınevi Kitabevi, Ankara, pp.519-523, 2022

2022

16. Juvenil Miyastenia Gravis

Özsoy Ö., Yiş U.

in: Temel Pediatrik Nöroloji Tanı ve Tedavi, Sefer Kumandaş,Mehmet Canpolat, Editor, Akademisyen Kitabevi, Ankara, pp.3047-3062, 2022

2022

17. Nöromuskuler Hastalıklara Tanısal Yaklaşım

POLAT A. İ., YİŞ U.

in: Temel Pediatrik Nöroloji Tanı ve Tedavi, Kumandaş Sefer, Canpolat Mehmet, Editor, Akademisyen Yayınevi, Ankara, pp.3207-3244, 2022

Funded Projects

2024 - Present

Yeni Tanı Alan SeLECTS Kendini sınırlayıcı sentrotemporal dikenli epilepsi sendromu Hastalarında miRNA134ün Tanı Tedavi ve İzlemdeki Rolü

Project Supported by Higher Education Institutions , BAP Research Project

GÜRSOY S. (Executive), GİRAY BOZKAYA Ö., ULUSOY E., ER A., ÖZTÜRK YILMAZ Ş., HIZ A. S., et al.

2024 - Present

Spinal Müsküler Atrofi Hastalığında Periferik Kan Mononükleer Hücrelerinden Elde Edilen Uzun Kodlanmayan RNA İçeriklerinin İncelenmesi

Project Supported by Higher Education Institutions , BAP Research Project

POLAT A. İ. (Executive), YİŞ U., HIZ A. S., GÜNAY Ç., SOYDEMİR D., OKTAY Y., et al.

2024 - 2027

PYROXD2: Mitokondriyal Hastalık Nedeni Bir Gen Olabilir mi?

Project Supported by Other Official Institutions

Polat A. İ. (Executive), Hız A. S., Yiş U., Oktay Y.

2024 - 2026

Pediatrik Migren Hastalarında Vestibüler Rehabilitasyonun Uygulanabilirliği ve Semptom, Denge, Yaşam ve Uyku Kalitesi Üzerine Etkisi

TUBITAK Project , 1002 - Quick Support Program

Tarsuslu T. (Executive), Yiş U.

2022 - 2024

Duchenne Muskuler DistrofiliHastalarda İkili Görevin Fonksiyonel Mobilite Üzerine Etkisi ve İkili Görev PerformansınınFonksiyonel Seviye ve Denge ile İlişkisi

TUBITAK Project , 1002 - Quick Support Program

Tarsuslu T. (Executive), Yiş U., Kurt Aydın M.

2020 - 2024

International Center for Genomic Medicine in Neuromuscular Disorders

Other International Funding Programs

Polat A. İ., Yayıcı Köken Ö., Hız A. S., Ceylan A. C., Güleç Ceylan G., Ardıçlı D., et al.

2019 - 2024

International Centre for Genomic Medicine in Neuromuscular Diseases

Project Supported by Public Organizations in Other Countries

Oktay Y., Yiş U. (Executive), Hız A. S.

2020 - 2023

Katanin-A benzeri protein 2 (Katanin-like 2) KATNAL2 geninde ilk kez görülen bir yanlış anlam mutasyonunun etkilerinin hasta fibroblastları ve bunlardan türetilen hücrelerde işlevsel analiz yöntemleri ile incelenmesi

TUBITAK Project , 1001 - Program for Supporting Scientific and Technological Research Projects

(Project Abstract)

Hız A. S. (Executive), Oktay Y., Yiş U.

2019 - 2021

An Integrative Approach Towards Improving the Diagnostic Yield of NGS Analysis in Pediatric Neurogenetic Diseases

Newton Programme Project , Katip Çelebi-Newton Fund, Other Project

Oktay Y. (Executive), Yiş U., Hız A. S., Arslan N.

2016 - 2020

Türkiye’de Akraba Evliliklerine Bağlı Nörogenetik Hastalık Yükünün Araştırılmasında Yeni Genomik Yaklaşımlar

Newton Programme Project , Katip Çelebi-Newton Fund, Other Project

Hız A. S. (Executive), Oktay Y., Yiş U., Arslan N., Güngör S., Yaramış A., et al.

2018 - 2019

Hiperoksi ilişkili apoptoz oluşturulan rat beyinlerinde Olesoxime (TRO19622) tedavisinin nöroprotektif etkisinin araştırılması

Project Supported by Higher Education Institutions , BAP Other

YİŞ U. (Executive)

2012 - 2014

SUBAKUT SKLEROZAN PANENSEFALİTLİ HASTALARDA MikroRNA-155, MikroRNA-146 ve MikroRNA-181 EKSPRESYONUNUN DEĞERLENDİRİLMESİ

Project Supported by Higher Education Institutions , BAP Research Project

YİŞ U. (Executive)

2012 - 2013

Çocukluk döneminde pentilentetrazol ile oluşturulan deneysel status epileptikus modelinde L-asetil karnitin, kafeik asit fenetil ester ve simvastatinin nöroprotektif etkinliğinin araştırılması

Project Supported by Higher Education Institutions , BAP Research Project

YİŞ U. (Executive)

2012 - 2012

Çocukluk döneminde pentilentetrazol ile oluşturulan deneysel status epileptikus modelinde L-asetil karnitin, kafeik asit fenetil ester ve simvastatinin nöroprotektif etkinliğinin araştırılması

Project Supported by Higher Education Institutions , BAP Research Project

Yiş U. (Executive), Özbal S.

Memberships and Roles in Scientific Organizations

2021 - Present

Türkiye Çocuk Nöroloji Derneği

Member

Scientific Consultations

2021 - Present

Scientific Consultancy

T.C Sağlık Bakanlığı

Dokuz Eylul University, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Turkey

2016 - Present

Scientific Consultancy

Dokuz Eylül Üniversitesi Tıp Fakültesi Girişimsel Etik Kurul

Dokuz Eylul University, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Turkey

Roles in Event Organizations

May 2024

1. Uluslarası Katılımlı İzmir Çocuk Kongresi

Scientific Congress

Yiş U., Hız A. S., Aydın A.

İzmir, Turkey

May 2024

Nörolojik Aciller Kursu

Scientific Congress

Yiş U., Hız A. S., Aydın A.

İzmir, Turkey

March 2024

Genç Meraklılar için Pediatrik Nöromusküler Hastalıklar Kursu

Scientific Congress

Yiş U.

İstanbul, Turkey

January 2024

Çocuk Nöroloji Pratiğinde Klinik Önemi Bilinmeyen Varyantlar (VUS) Sorunu ve Çözüm Önerileri

Scientific Congress

Yiş U., Hız A. S., Polat A. İ., Aydın A.

İzmir, Turkey

September 2023

International Pediatric Neurology Online Symposium

Scientific Congress

Yiş U., Hız A. S., Aydın A., Polat A. İ.

Turkey

March 2023

Genç Meraklılar İçin Pediatrik Nöromusküler Hastalıklar Kursu

Scientific Congress

Yiş U.

Turkey

Awards

October 2022

ICNA Best E-Poster Presentation Award inNeuromuscular

International Child Neurology Assosication

October 2022

Neuromuscular Diseases In The Pediatric Intensive Care Unit: 11 Years Of Experience From A Tertiary Children's Hospital, ICNA Best Platform Presentation Award in Neuromuscular

International Child Neurology Association

April 2009

Araştırma Birincilik Ödülü

17. Ulusal Neonatoloji Kongresi (Uneko-17)

Congress and Symposium Activities

20 November 2024 - 20 November 2024

68. Türkiye Milli Pediatri Kongresi ve 1. Uluslararası Türkiye Milli Pediatri Derneği Kongresi,

Invited Speaker

Antalya-Turkey

24 October 2024 - 24 October 2024

Nörolojik Hastalıklar ve Görülen beslenme Sorunları

Invited Speaker

İzmir-Turkey

08 October 2024 - 12 October 2024

29 th Annual Congress of World Muscle Society

Audience

Praha-Czech Republic

05 October 2024 - 05 October 2024

7. PEDİATRİK NÖROİMMÜNOLOJİ SEMPOZYUMU

Invited Speaker

Ankara-Turkey

24 September 2024 - 24 September 2024

5 yıllık klinik çalışma sonuçları ışığında risdiplam

Attendee

İstanbul-Turkey

19 September 2024 - 21 September 2024

7. nöromusküler hastalıklar kongresi

Invited Speaker

Nevşehir-Turkey

11 September 2024 - 11 September 2024

Duchenne musküler distrofi konuşuyoruz

Invited Speaker

İzmir-Turkey

20 June 2023 - 24 June 2023

EPNS Congress 2023

Audience

Praha-Czech Republic

28 March 2023 - 31 March 2023

UK Neuromuscular Translational Research Conference

Attendee

London-England

15 March 2023 - 19 March 2023