Metrics
Publication
523
Open Access
52
UN Sustainable Development Goals
Announcements & Documents
Download File
Education
2005 - 2008
2005 - 2008Post Doctorate of Medicine
Dokuz Eylul University, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Turkey
2000 - 2005
2000 - 2005Expertise In Medicine
Dokuz Eylul University, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Turkey
1994 - 2000
1994 - 2000Undergraduate
Ege University, Faculty Of Medicine, Tıp Pr., Turkey
Research Areas
Health Sciences
Academic Positions
2011 - Present
2011 - PresentProfessor
Dokuz Eylul University, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü
2011 - Present
2011 - PresentProfessor
Dokuz Eylul University, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü
2011 - 2016
2011 - 2016Associate Professor
Dokuz Eylul University, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü
Managerial Experience
2025 - Present
2025 - PresentTürkiye Çocuk Nörolojisi Dernek Başkanı
Dokuz Eylul University, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü
2020 - Present
2020 - PresentHead of Department
Dokuz Eylul University, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü
Supervised Theses
2020
2020Expertise 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
2019Expertise 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
2015Expertise In Medicine
Evaluation of autonomic dysfunction in pediatric migraine patients
YİŞ U. (Advisor)
D.ELİTEZ(Student)
Articles
All (265)
SCI-E, SSCI, AHCI (215)
SCI-E, SSCI, AHCI, ESCI (237)
ESCI (23)
Scopus (233)
TRDizin (47)
Other Indexes (5)
2025
20251. 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)
2025
20252. 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)
2025
20253. 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
, 2025 (SCI-Expanded)
2025
20254. 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)
2025
20255. 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)
2025
20256. 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)
2025
20257. 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)
2025
20258. 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)
2025
20259. 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)
2025
202510. 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)
2025
202511. 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)
2025
202512. 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)
2025
202513. 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)
2025
202514. 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)
2025
202515. 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)
2025
202516. 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
, 2025 (SCI-Expanded)
2025
202517. 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
, 2025 (SCI-Expanded)
2025
202518. 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)
2024
202419. 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)
2024
202420. 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)
2024
202421. 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)
2024
202422. 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)
2024
202423. 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)
2024
202424. 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)
2024
202425. 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)
2024
202426. 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)
2024
202427. 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)
2024
202428. Periferik Sinir Hastalıkları: Herediter Nöropatiler
Yiş U., Paketçi C.
Türkiye Klinikleri Pediatri Dergisi , pp.37-41, 2024 (Peer-Reviewed Journal)
2024
202429. 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 (Peer-Reviewed Journal)
2024
202430. 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)
2024
202431. 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)
2024
202432. 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)
2023
202333. 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)
2023
202334. 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)
2023
202335. 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)
2023
202336. 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)
2023
202337. 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)
2023
202338. 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)
2023
202339. 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)
2023
202340. 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 (Peer-Reviewed Journal)
2023
202341. 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
202342. 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)
2023
202343. 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)
2023
202344. 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)
2023
202345. 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)
2023
202346. 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)
2023
202347. 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)
2023
202348. 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)
2023
202349. 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)
2023
202350. 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)
2023
202351. 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)
2023
202352. 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)
2023
202353. 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)
2023
202354. 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)
2023
202355. 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)
2023
202356. 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)
2023
202357. 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)
2023
202358. 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)
2023
202359. 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)
2023
202360. 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 (Peer-Reviewed Journal)
2023
202361. 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)
2022
202262. 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)
2022
202263. 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)
2022
202264. 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)
2022
202265. 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 (Peer-Reviewed Journal)
2022
202266. 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)
2022
202267. 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)
2022
202268. 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)
2022
202269. 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)
2022
202270. 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)
2022
202271. 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)
2022
202272. 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)
2022
202273. 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)
2022
202274. 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)
2022
202275. 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)
2022
202276. 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
202277. 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)
2022
202278. 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)
2022
202279. 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
202280. 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)
2021
202181. 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)
2021
202182. 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)
2021
202183. 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
202184. 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)
2021
202185. 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)
2021
202186. 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)
2021
202187. 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)
2021
202188. 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)
2021
202189. 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)
2021
202190. 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 (Peer-Reviewed Journal)
2021
202191. 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)
2021
202192. 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)
2021
202193. 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)
2021
202194. 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 (Peer-Reviewed Journal)
2021
202195. 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 (Peer-Reviewed Journal)
2021
202196. 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)
2021
202197. 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)
2021
202198. 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)
2020
202099. 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)
2020
2020100. 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)
2020
2020101. 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)
2020
2020102. 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)
2020
2020103. 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)
2020
2020104. 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)
2020
2020105. 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)
2020
2020106. 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)
2020
2020107. 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)
2020
2020108. 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)
2020
2020109. 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)
2020
2020110. 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)
2020
2020111. 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)
2020
2020112. 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)
2019
2019113. 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)
2019
2019114. 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)
2019
2019115. 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)
2019
2019116. 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)
2019
2019117. 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)
2019
2019118. 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)
2019
2019119. 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)
2019
2019120. 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)
2019
2019121. 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)
2019
2019122. 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)
2018
2018123. 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)
2018
2018124. Hypertrophic Neuropathy of the Sciatic Nerve
YİŞ U., Arslan M., Gulleryuz H.
PEDIATRIC NEUROLOGY
, vol.87, pp.77, 2018 (SCI-Expanded)
2018
2018125. 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)
2018
2018126. 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
2018127. 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)
2018
2018128. 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)
2018
2018129. 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)
2018
2018130. A boy with neck weakness
YİŞ U., Becker K., Cirak S.
NEUROMUSCULAR DISORDERS
, vol.28, no.3, pp.236-237, 2018 (SCI-Expanded)
2018
2018131. 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
2017132. 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)
2017
2017133. 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)
2017
2017134. 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)
2017
2017135. 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)
2017
2017136. 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)
2017
2017137. 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)
2017
2017138. 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)
2017
2017139. 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)
2017
2017140. 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)
2017
2017141. 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)
2017
2017142. 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)
2017
2017143. 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)
2016
2016144. 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)
2016
2016145. 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)
2016
2016146. 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)
2016
2016147. 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)
2016
2016148. 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)
2016
2016149. 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)
2016
2016150. 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)
2016
2016151. 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)
2015
2015152. 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)
2015
2015153. 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)
2015
2015154. 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)
2015
2015155. 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)
2015
2015156. 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)
2015
2015157. 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)
2015
2015158. 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)
2015
2015159. 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)
2015
2015160. 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)
2015
2015161. 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)
2015
2015162. 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)
2015
2015163. 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)
2015
2015164. 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)
2015
2015165. 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 (Peer-Reviewed Journal)
2015
2015166. 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
2015167. 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)
2015
2015168. 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)
2014
2014169. 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 (Peer-Reviewed Journal)
2014
2014170. 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)
2014
2014171. 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)
2014
2014172. 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)
2014
2014173. 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)
2014
2014174. 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)
2014
2014175. 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)
2014
2014176. 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)
2014
2014177. 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)
2014
2014178. 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)
2014
2014179. 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)
2014
2014180. 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)
2014
2014181. 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
2014182. 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 (Peer-Reviewed Journal)
2014
2014183. 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 (Peer-Reviewed Journal)
2014
2014184. 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)
2014
2014185. 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)
2014
2014186. 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)
2014
2014187. 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)
2014
2014188. 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)
2014
2014189. 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)
2014
2014190. 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
2014191. 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)
2014
2014192. 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)
2013
2013193. 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)
2013
2013194. 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)
2013
2013195. 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)
2013
2013196. 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)
2013
2013197. 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)
2013
2013198. 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)
2013
2013199. 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 (Peer-Reviewed Journal)
2013
2013200. 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)
2013
2013201. 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)
2013
2013202. 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 (Peer-Reviewed Journal)
2013
2013203. 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)
2013
2013204. 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)
2013
2013205. 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 (Peer-Reviewed Journal)
2013
2013206. 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)
2013
2013207. 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)
2013
2013208. 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)
2013
2013209. 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)
2013
2013210. 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)
2013
2013211. 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)
2013
2013212. 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)
2012
2012213. 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)
2012
2012214. 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)
2012
2012215. 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)
2012
2012216. 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 (Peer-Reviewed Journal)
2012
2012217. 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)
2011
2011218. 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)
2011
2011219. 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)
2011
2011220. 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)
2010
2010221. 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)
2010
2010222. 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)
2010
2010223. 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)
2010
2010224. 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)
2010
2010225. 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)
2010
2010226. 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)
2009
2009227. 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)
2009
2009228. 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)
2009
2009229. 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)
2009
2009230. 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)
2009
2009231. 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
2009232. 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)
2009
2009233. 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)
2009
2009234. 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)
2009
2009235. 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)
2009
2009236. 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)
2009
2009237. 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)
2009
2009238. 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)
2009
2009239. Nonketotic Hyperglycinemia and Acquired Hydrocephalus
Yis U., Kurul S. H., Dirik E.
PEDIATRIC NEUROLOGY
, vol.40, no.2, pp.138-140, 2009 (SCI-Expanded)
2009
2009240. 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)
2009
2009241. 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)
2008
2008242. 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)
2008
2008243. 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)
2008
2008244. 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)
2008
2008245. 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)
2008
2008246. 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)
2008
2008247. 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)
2008
2008248. 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)
2008
2008249. 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)
2008
2008250. 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)
2008
2008251. 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)
2008
2008252. 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)
2007
2007253. 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)
2007
2007254. 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)
2007
2007255. 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)
2007
2007256. 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)
2007
2007257. 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)
2006
2006258. 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)
2006
2006259. 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)
2005
2005260. Recurrent parotitis in a seven year-old boy
Yis U., Unal N.
INDIAN PEDIATRICS
, vol.42, no.9, pp.958-959, 2005 (SCI-Expanded)
2005
2005261. 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)
2005
2005262. 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)
2005
2005263. Primary lymphedema in a four-year-old boy
Yis U., Dirik E.
INDIAN PEDIATRICS
, vol.42, no.7, pp.726-728, 2005 (SCI-Expanded)
2005
2005264. 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)
2005
2005265. 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
2024
20241. 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
20242. 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
20243. 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
20244. 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
20245. 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)
2024
20246. 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)
2023
20237. 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
20238. 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
20239. 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
202210. 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
202211. 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
202212. 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
202213. 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
202214. 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
202215. 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
202216. 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
202217. 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
202218. 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
202219. 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
202220. 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
202221. 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
202222. 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
202223. 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
202224. 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
202225. 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
202126. 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
202127. 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
202128. 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
202129. 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
202130. 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
202131. 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
202132. 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
202133. 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
202134. 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
202135. 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
201336. 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
202137. 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
202138. 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
202239. 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
202140. 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
202141. 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)
2021
202142. 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)
2020
202043. 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
202044. 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
202045. 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
202046. 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
202047. 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
202048. 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
202049. 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
202050. 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
202051. 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
201952. 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
201953. 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)
2019
201954. 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)
2022
202255. 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
201956. 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
201957. 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
201958. 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
201959. 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
201960. 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
201961. 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
201962. 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
201963. 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
201964. 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
201965. 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
201966. 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
201967. 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
201968. 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
201969. 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
201970. 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
201971. 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
201972. 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
201973. 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
201874. 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
201875. 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
201876. 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
201877. 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
201878. 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
201879. 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
201880. 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
201881. 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
201882. 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)
2018
201883. 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
201884. 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
201885. 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
201886. 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
201887. 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)
2017
201788. 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
201789. 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
201790. 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
201791. 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
201792. 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
201793. 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
201794. 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
201795. 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
201796. 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
201797. 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
201798. 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
201799. 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
2017100. 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
2017101. 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
2017102. 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
2017103. 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
2017104. 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
2017105. 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
2017106. 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
2017107. 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
2017108. 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
2017109. 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
2017110. 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)
2016
2016111. 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
2016112. 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
2016113. 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
2016114. 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
2016115. 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
2016116. 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
2016117. 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
2016118. 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
2016119. 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
2016120. 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
2016121. 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
2016122. 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
2016123. 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
2016124. 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
2016125. 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
2016126. 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
2016127. 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
2015128. 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
2015129. 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
2015130. 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
2015131. 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
2015132. 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
2015133. 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
2015134. 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
2015135. 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
2015136. 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
2015137. 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
2015138. 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
2015139. 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)
2015
2015140. 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
2015141. 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
2015142. 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
2015143. 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
2015144. 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
2015145. 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
2015146. 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)
2019
2019147. 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
2015148. 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
2015149. 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
2015150. 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
2015151. intrakraniyal enfeksiyonlar
YİŞ U.
16. DEÜTF Pediatri Günleri, Turkey, 12 - 13 March 2015
2015
2015152. 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
2015153. 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)
2015
2015154. 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)
2014
2014155. 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
2014156. 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
2014157. 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
2014158. 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
2014159. 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
2014160. 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
2014161. 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
2014162. 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
2014163. 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
2014164. 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
2014165. 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
2014166. 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
2014167. 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
2014168. 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
2014169. 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
2014170. 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
2014171. 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
2014172. 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
2014173. 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
2014174. 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
2013175. 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
2013176. 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
2013177. 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
2013178. 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
2013179. 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
2013180. 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
2013181. 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
2013182. 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
2013183. 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
2013184. 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
2013185. 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
2013186. 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
2013187. 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
2013188. 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
2013189. 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
2013190. 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
2012191. 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
2012192. 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
2012193. 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
2012194. 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
2012195. 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
2012196. 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
2012197. 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
2012198. 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
2012199. 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
2022200. 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
2012201. 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
2010202. 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
2010203. 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
2008204. 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
2008205. 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
2007206. 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)
2007
2007207. 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)
2005
2005208. 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
2014209. 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
2023
20231. 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
20232. 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
20233. 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
20224. 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
20225. "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
20226. 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
20227. 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
20228. 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
20229. 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
202210. 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
202211. 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
2022 - 2024
2022 - 2024Duchenne 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
2020 - 2024International 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
2019 - 2024International 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
2020 - 2023Katanin-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
2019 - 2021An 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
2016 - 2020Türkiye’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
2018 - 2019Hiperoksi ilişkili apoptoz oluşturulan rat beyinlerinde Olesoxime (TRO19622) tedavisinin nöroprotektif etkisinin araştırılması
Project Supported by Higher Education Institutions , BAP Other
YİŞ U. (Executive)
2012 - 2014
2012 - 2014SUBAKUT 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
2012 - 2013Çocukluk 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)
Memberships and Roles in Scientific Organizations
2021 - Present
2021 - PresentTürkiye Çocuk Nöroloji Derneği
Member
Scientific Consultations
2021 - Present
2021 - PresentScientific Consultancy
T.C Sağlık Bakanlığı
Dokuz Eylul University, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Turkey
2016 - Present
2016 - PresentScientific 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
May 20241. Uluslarası Katılımlı İzmir Çocuk Kongresi
Scientific Congress
Yiş U., Hız A. S., Aydın A.
İzmir, Turkey
May 2024
May 2024Nörolojik Aciller Kursu
Scientific Congress
Yiş U., Hız A. S., Aydın A.
İzmir, Turkey
March 2024
March 2024Genç Meraklılar için Pediatrik Nöromusküler Hastalıklar Kursu
Scientific Congress
Yiş U.
İstanbul, Turkey
January 2024
January 2024Çocuk 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
September 2023International Pediatric Neurology Online Symposium
Scientific Congress
Yiş U., Hız A. S., Aydın A., Polat A. İ.
Turkey
March 2023
March 2023Genç Meraklılar İçin Pediatrik Nöromusküler Hastalıklar Kursu
Scientific Congress
Yiş U.
Turkey
Awards
October 2022
October 2022Neuromuscular 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
October 2022
October 2022ICNA Best E-Poster Presentation Award inNeuromuscular
International Child Neurology Assosication
Congress and Symposium Activities
20 November 2024 - 20 November 2024
20 November 2024 - 20 November 202468. Türkiye Milli Pediatri Kongresi ve 1. Uluslararası Türkiye Milli Pediatri Derneği Kongresi,
Invited Speaker
Antalya-Turkey
24 October 2024 - 24 October 2024
24 October 2024 - 24 October 2024Nörolojik Hastalıklar ve Görülen beslenme Sorunları
Invited Speaker
İzmir-Turkey
08 October 2024 - 12 October 2024
08 October 2024 - 12 October 202429 th Annual Congress of World Muscle Society
Audience
Praha-Czech Republic
05 October 2024 - 05 October 2024
05 October 2024 - 05 October 20247. PEDİATRİK NÖROİMMÜNOLOJİ SEMPOZYUMU
Invited Speaker
Ankara-Turkey
24 September 2024 - 24 September 2024
24 September 2024 - 24 September 20245 yıllık klinik çalışma sonuçları ışığında risdiplam
Attendee
İstanbul-Turkey
19 September 2024 - 21 September 2024
19 September 2024 - 21 September 20247. nöromusküler hastalıklar kongresi
Invited Speaker
Nevşehir-Turkey
11 September 2024 - 11 September 2024
11 September 2024 - 11 September 2024Duchenne musküler distrofi konuşuyoruz
Invited Speaker
İzmir-Turkey
20 June 2023 - 24 June 2023
20 June 2023 - 24 June 2023EPNS Congress 2023
Audience
Praha-Czech Republic
28 March 2023 - 31 March 2023
28 March 2023 - 31 March 2023UK Neuromuscular Translational Research Conference
Attendee
London-England
15 March 2023 - 19 March 2023
15 March 2023 - 19 March 2023