Prof. Dr. KORCAN DEMİR

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Aromatase inhibitors: a useful additional therapeutic option for slowing down advanced bone age in boys with growth hormone deficiency

Akın Kağızmanlı G., Özalp Kızılay D., Besci Ö., Yüksek Acinikli K., Özen S., Demir K., et al.

JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , cilt.47, sa.5, ss.1227-1235, 2024 (SCI-Expanded)

Comprehensive Insights into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes with a Multicenter Approach.

Şıklar Z., Özsu E., Kızılcan Çetin S., Özen S., Çizmecioğlu-Jones F., Balkı H. G., et al.

Journal of clinical research in pediatric endocrinology , 2024 (SCI-Expanded)

High frequency of transient congenital hypothyroidism among infants referred for suspected congenital hypothyroidism from the Turkish National screening program: thyroxine dose may guide the prediction of transients.

Özer Y., Anık A., Sayılı U., Tercan U., Deveci Sevim R., Güneş S., et al.

Journal of endocrinological investigation , 2024 (SCI-Expanded)

Salivary Sex Steroid Levels in Infants and Their Relation with Infantile Colic.

Mete Kalaycı F., Gürsoy Doruk Ö., Erbaş İ. M., İnce O. T., Tan M. N., Aydın A., et al.

Journal of clinical research in pediatric endocrinology , 2024 (SCI-Expanded)

Aromatase Inhibitors May Increase the Risk of Cardiometabolic Complications in Adolescent Boys

Besci Ö., Akçura Y. D., Acinikli K., Kağızmanlı G. A., Demir K., Böber E., et al.

PEDIATRIC CARDIOLOGY , cilt.45, sa.2, ss.228-239, 2024 (SCI-Expanded)

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

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

Clinical endocrinology , 2023 (SCI-Expanded)

Atypical Presentation and Course of ACTH-independent Cushing's Syndrome in Two Families.

Yüksek Acinikli K., Acar S., Paketçi A., Kırbıyık Ö., Erbaş M., Besci Ö., et al.

Journal of clinical research in pediatric endocrinology , 2023 (SCI-Expanded)

Clinical Characteristics of Children with Combined Pituitary Hormone Deficiency and the Effects of Growth Hormone Treatment.

Besci Ö., Sevim R. D., Acinikli K. Y., Demir K., Çatlı G., Özhan B., et al.

Klinische Padiatrie , 2023 (SCI-Expanded)

Deciphering the Clinical Presentations in LMNA-related Lipodystrophy: Report of 115 Cases and a Systematic Review

Besci O., Foss de Freitas M. C., Guidorizzi N. R., Guler M. C., Gilio D., Maung J. N., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , 2023 (SCI-Expanded)

Long-term follow-up results and treatment outcomes of children and adults with resistance to thyroid hormone alpha

ERBAŞ İ. C., Çakır M., YENER A. S., DEMİR K.

JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , cilt.46, sa.9, ss.1855-1863, 2023 (SCI-Expanded)

A National Multicenter Study of Leptin and Leptin Receptor Deficiency and Systematic Review

Besci Ö., Firat S. N., Özen S., Çetinkaya S., Akın L., Kör Y., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , cilt.108, sa.9, ss.2371-2388, 2023 (SCI-Expanded) Sürdürülebilir Kalkınma

Aromatase inhibitors: an effective and safe option for height increment in boys with growth hormone deficiency?

AKIN KAĞIZMANLI G., Kizilay D. O., Besci O., Acinikli K. Y., Ozen S., DEMİR K., et al.

HORMONE RESEARCH IN PAEDIATRICS , ss.89, 2023 (SCI-Expanded)

Which method is more effective in predicting adult height in pubertal girls treated with gonadotropin-releasing hormone agonist?

Akın Kağızmanlı G., Deveci Sevim R., Besci Ö., Yüksek Acinikli K., Buran A. H., Erbaş İ. M., et al.

HORMONES-INTERNATIONAL JOURNAL OF ENDOCRINOLOGY AND METABOLISM , cilt.22, sa.3, ss.501-506, 2023 (SCI-Expanded)

Growth Hormone Dosing Estimations Based on Body Weight Versus Body Surface Area.

Besci Ö., Deveci Sevim R., Yüksek Acinikli K., Akın Kağızmanlı G., Ersoy S., Demir K., et al.

Journal of clinical research in pediatric endocrinology , cilt.15, sa.3, ss.268-275, 2023 (SCI-Expanded)

Decline in the Age of Menarche in Istanbul Schoolgirls Over the Last 12 Years

Guran T., Helvacioglu D., Gurpinar Tosun B., Yavas Abali Z., Alir F., Arslan Y. T., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.15, sa.2, ss.154-159, 2023 (SCI-Expanded)

Positive effects of ketogenic diet on weight control in children with obesity due to Prader-Willi syndrome

Teke Kısa P., Güzel O., ARSLAN N., DEMİR K.

CLINICAL ENDOCRINOLOGY , cilt.98, sa.3, ss.332-341, 2023 (SCI-Expanded)

Adverse Events Associated with COVID-19 Vaccination in Adolescents with Endocrinological Disorders: A Cross-Sectional Study

Erbaş İ. M., Erbaş İ. C., Kağızmanlı G. A., Yüksek Acinikli K., Besci Ö., Demir K., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.15, sa.3, ss.248-256, 2023 (SCI-Expanded)

Efficacy of aromatase inhibitor therapy in a case with large cell calcifying Sertoli cell tumour-associated prepubertal gynaecomastia

AKIN KAĞIZMANLI G., BESCİ Ö., YÜKSEK ACİNİKLİ K., ŞEKER G., YAŞAR E., ÖZTÜRK Y., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , sa.12, ss.1565-1570, 2022 (SCI-Expanded)

Hemoglobin A(1C) can differentiate subjects with GCK mutations among patients suspected to have MODY.

Yılmaz Uzman C., Erbaş İ. M., Giray Bozkaya Ö., Paketçi A., Çağlayan A. O., Abacı A., et al.

Journal of pediatric endocrinology & metabolism : JPEM , cilt.35, sa.12, ss.1528-1536, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

Biochemical indicators of euthyroid sick syndrome in critically ill children.

Besci T., Besci Ö., Arslan G., Ilgaz H., Prencuva P., Özdemir G., et al.

Journal of pediatric endocrinology & metabolism : JPEM , cilt.35, sa.10, ss.1285-1292, 2022 (SCI-Expanded)

A Rare and Treatable Cause of Prepubertal Gynecomastia: Large Cell Calcifying Sertoli Cell Tumor

AKIN KAĞIZMANLI G., BESCİ Ö., YÜKSEK ACİNİKLİ K., ŞEKER G., YAŞAR E., ÖZTÜRK Y., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.95, sa.SUPPL 2, ss.393-394, 2022 (SCI-Expanded)

Genotype, phenotype characteristics and long-term follow-up of patients with Vitamin D Dependent Rickets Type IA (VDDR1a): A nationwide multicentre retrospective cross-sectional study

Cayir A., DEMİRBİLEK H., TÜRKYILMAZ A., DEMİRCİOĞLU S., BEREKET A., Darendeliler F., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.95, sa.SUPPL 2, ss.100, 2022 (SCI-Expanded)

Clinical course of primary empty sella in children: a single- center experience

BESCİ Ö., YAŞAR E., ERBAŞ İ. M., Acimkli K. Y., DEMİR K., BÖBER E., et al.

TURKISH JOURNAL OF PEDIATRICS , cilt.64, sa.5, ss.900-908, 2022 (SCI-Expanded)

Atypical comorbidities in a child considered to have type 1 diabetes led to the diagnosis of SLC29A3 spectrum disorder

Besci Ö., Patel K. A., Yıldız G., Tüfekçi Ö., Yüksek Acinikli K., Erbaş İ. M., et al.

HORMONES-INTERNATIONAL JOURNAL OF ENDOCRINOLOGY AND METABOLISM , cilt.21, sa.3, ss.501-506, 2022 (SCI-Expanded)

A National Multicenter Study of Leptin (LEP) and Leptin Receptor (LEPR) Deficiency and a Systematic Review of Patients with Pathogenic LEP/LEPR Variants

BESCİ Ö., Firat S. N., ÖZEN S., Cetinkaya S., Akin L., Kor Y., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.95, sa.SUPPL 2, ss.239, 2022 (SCI-Expanded)

Salivary Sex Steroid Levels in Infants During Minipuberty and Their Relationship with Infantile Colic

METE KALAYCI F., GÜRSOY DORUK Ö., ERBAŞ İ. M., İNCE O. T., TAN M. N., AYDIN A., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.95, sa.SUPPL 2, ss.256-257, 2022 (SCI-Expanded)

Outcomes of four patients with osteonecrosis after one-year pamidronate treatment

Yüksek Acinikli K., Besci Ö., Yaşar E., Tüfekçi Ö., Karadag Z., Yıldız G., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.95, sa.SUPPL 2, ss.144-145, 2022 (SCI-Expanded)

Biochemical Indicators of Euthyroid Sick Syndrome in Critically Ill Children

BESCİ T., BESCİ Ö., ARSLAN G., ILGAZ H., PRENCUVA P., ÖZDEMİR G., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.95, sa.SUPPL 2, ss.413, 2022 (SCI-Expanded)

Has the Frequency of Precocious Puberty and Rapidly Progressive Early Puberty Increased in Girls During the COVID-19 Pandemic?

Acinikli K., Erbaş İ. M., Besci Ö., Demir K., Abacı A., Böber E.

Journal of clinical research in pediatric endocrinology , cilt.14, sa.3, ss.302-307, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

Low Complement C1q/TNF-related Protein-13 Levels are Associated with Childhood Obesity But not Binge Eating Disorder

ERBAŞ İ. M., PAKETÇİ A., TURAN S., Sisman A., DEMİR K., BÖBER E., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.14, sa.2, ss.179-187, 2022 (SCI-Expanded)

The effect of leisure boredom and A1C level on diabetes eating problems in adolescents with type 1 diabetes

Gürkan K. P., Ayar D., Karadağ G., Böber E., Demir K.

JOURNAL OF PEDIATRIC NURSING-NURSING CARE OF CHILDREN & FAMILIES , cilt.64, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

Initial neutrophil/lymphocyte and lymphocyte/monocyte ratios can predict future insulin need in newly diagnosed type 1 diabetes mellitus

Erbas I. M., Hajikhanova A., BESCİ Ö., Acinikli K. Y., DEMİR K., BÖBER E., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.35, sa.5, ss.593-602, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

Steroid Hormone Profiles and Molecular Diagnostic Tools in Pediatric Patients With non-CAH Primary Adrenal Insufficiency

SEVEN MENEVŞE T., Demirkol Y. K., GÜRPINAR TOSUN B., Bayramoglu E., YILDIZ M., Acar S., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , cilt.107, sa.5, 2022 (SCI-Expanded)

MANF supports the inner hair cell synapse and the outer hair cell stereocilia bundle in the cochlea

Ikaheimo K., Herranen A., Iivanainen V., Lankinen T., Aarnisalo A. A., Sivonen V., et al.

LIFE SCIENCE ALLIANCE , cilt.5, sa.2, 2022 (SCI-Expanded)

Systematic genetic testing for recessively inherited monogenic diabetes: a cross-sectional study in paediatric diabetes clinics

Patel K. A., Ozbek M. N., Yildiz M., GÜRAN T., Kocyigit C., ACAR S., et al.

DIABETOLOGIA , cilt.65, sa.2, ss.336-342, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

DLG2 Mutations in the Etiology of Pubertal Delay and Idiopathic Hypogonadotropic Hypogonadism

TURAN İ., DEMİR K., Mengen E., KOTAN L. D., GÜRBÜZ F., YÜKSEL B., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.94, sa.9-10, ss.364-368, 2022 (SCI-Expanded)

RABSON-MENDENHALL SYNDROME AND MEDULLARY SPONGE KIDNEY: A CASE REPORT

YILDIZ G., Bayram M. T., BESCİ Ö., GÜLERYÜZ UÇAR H., DEMİR K., KAVUKÇU S., et al.

PEDIATRIC NEPHROLOGY , cilt.36, sa.10, ss.3423, 2021 (SCI-Expanded)

GLOMERULAR INVOLVEMENT AS IGA NEPHROPATHY IN A CHILD WITH H SYNDROME

BESCİ Ö., Patel K. A., YILDIZ G., TÜFEKÇİ Ö., YÜKSEK ACİNİKLİ K., ERBAŞ İ. M., et al.

PEDIATRIC NEPHROLOGY , cilt.36, sa.10, ss.3442-3443, 2021 (SCI-Expanded)

Circulating C1q Complement/TNF-Related Protein (CTRP)-13 Levels in Obese Children and Its Relationship with Metabolic Disorders

ERBAŞ İ. M., PAKETÇİ A., TURAN S., Sisman A., DEMİR K., BÖBER E., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.94, sa.SUPPL 1, ss.128, 2021 (SCI-Expanded)

Adrenocortical hormone profiles do not predict the molecular etiology in non-CAH primary adrenal insufficiency

SEVEN MENEVŞE T., Demirkol Y. K., GÜRPINAR TOSUN B., Bayramoglu E., Yildiz M., Acar S., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.94, sa.SUPPL 1, ss.64-65, 2021 (SCI-Expanded)

Clinical course of primary empty sella in children: a 10-year single-center experience

BESCİ Ö., YAŞAR E., ERBAŞ İ. M., YÜKSEK ACİNİKLİ K., DEMİR K., BÖBER E., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.94, sa.SUPPL 1, ss.355, 2021 (SCI-Expanded)

Initial Neutrophil/Lymphocyte and Lymphocyte/Monocyte Ratios Can Predict Future Insulin Need in Newly Diagnosed Type 1 Diabetes Mellitus

ERBAŞ İ. M., HAJIKHANOVA A., BESCİ Ö., YÜKSEK ACİNİKLİ K., DEMİR K., BÖBER E., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.94, sa.SUPPL 1, ss.100, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

Serum Sex Hormone Binding Globulin Levels, but not 4-Hour Profile of 17-OH Progesterone, Would be Useful in Monitoring Children with Congenital Adrenal Hyperplasia

Besci Ö., Erbaş İ. M., Küme T., Yüksek Acinikli K., Abacı A., Böber E., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.94, sa.SUPPL 1, ss.179-180, 2021 (SCI-Expanded)

Comparison of the Effectiveness of Adult Height Prediction Methods in Children with Growth Hormone Deficiency

ERBAŞ İ. M., ÖLMEZ Z., Paketci A., DEMİR K., BÖBER E., ABACI A.

ENDOCRINE RESEARCH , cilt.46, sa.3, ss.140-147, 2021 (SCI-Expanded)

Bedside sonographic measurements of optic nerve sheath diameter in children with diabetic ketoacidosis

Sik N., ERBAŞ İ. M., DEMİR K., YILMAZ D., DUMAN M.

PEDIATRIC DIABETES , cilt.22, sa.4, ss.618-624, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

Social anxiety levels and self-efficacy perceptions of adolescents with type-1 diabetes predict smoking outcome expectations: a cross-sectional study

GÜRKAN K. P., AYAR D., BEKTAŞ M., BÖBER E., DEMİR K.

JOURNAL OF SUBSTANCE USE , cilt.26, sa.3, ss.299-305, 2021 (SSCI) Sürdürülebilir Kalkınma

Loss of MANF Causes Childhood-Onset Syndromic Diabetes Due to Increased Endoplasmic Reticulum Stress

Montaser H., Patel K. A., Balboa D., Ibrahim H., Lithovius V., Naatanen A., et al.

DIABETES , cilt.70, sa.4, ss.1006-1018, 2021 (SCI-Expanded)

DLG2 Mutations in Hypogonadotropic Hypogonadism

KOTAN L. D., DEMİR K., Turan I., Topaloglu A. K.

NEUROENDOCRINOLOGY , cilt.111, ss.12, 2021 (SCI-Expanded)

The Clinical Spectrum of Resistance to Thyroid Hormone Alpha in Children and Adults

ERBAŞ İ. M., DEMİR K.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.13, sa.1, ss.1-14, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

The relationship of carotid intima-media thickness with anthropometric and metabolic parameters in patients with classic congenital adrenal hyperplasia

ÜNVER TUHAN H., ÖZTÜRK ATASOY T., ÇATLI G., ACAR S., ABACI A., ÜÇÜNCÜ EGELİ T., et al.

TURKISH JOURNAL OF MEDICAL SCIENCES , cilt.51, sa.4, ss.1738-1746, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

Detection of SHOX Gene Variations in Patients with Skeletal Abnormalities with or without Short Stature

Gursoy S., Hazan F., AYKUT A., Nalbantoglu O., Korkmaz H. A., DEMİR K., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.12, sa.4, ss.358-365, 2020 (SCI-Expanded)

A nonsense variant in FGFR1: a rare cause of combined pituitary hormone deficiency

ERBAŞ İ. M., Paketci A., Acar S., KOTAN L. D., DEMİR K., ABACI A., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.33, sa.12, ss.1613-1615, 2020 (SCI-Expanded)

A novel compound heterozygous variant in CYP19A1 resulting in aromatase deficiency with normal ovarian tissue

Acar S., ERBAŞ İ. M., Paketci A., Onay H., ÇANKAYA T., Gursoy S., et al.

TURKISH JOURNAL OF PEDIATRICS , cilt.62, sa.5, ss.826-830, 2020 (SCI-Expanded)

Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study

Groeneweg S., van Geest F. S., ABACI A., Alcantud A., Ambegaonkar G. P., Armour C. M., et al.

LANCET DIABETES & ENDOCRINOLOGY , cilt.8, sa.7, ss.594-605, 2020 (SCI-Expanded)

New Features for Child Metrics: Further Growth References and Blood Pressure Calculations

DEMİR K., KONAKÇI E., ÖZKAYA G., DEMİR B. K., ÖZEN S., Aydin M., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.12, sa.2, ss.125-129, 2020 (SCI-Expanded)

Nationwide Turkish Cohort Study of Hypophosphatemic Rickets

ŞIKLAR Z., DEMİRCİOĞLU S., BEREKET A., BAŞ F., GÜRAN T., Akberzade A., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.12, sa.2, ss.150-159, 2020 (SCI-Expanded)

Serum Level of Biotin Rather than the Daily Dosage Is the Main Determinant of Interference on Thyroid Function Assays

Paketci A., Kose E., Calan Ö., Acar S., Teke P., Demirci F., et al.

HORMONE RESEARCH IN PAEDIATRICS , sa.2, ss.92-98, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma

NOVEL VDR MUTATIONS IN PATIENTS WITH VITAMIN D-DEPENDENT RICKETS TYPE 2A: A MILD DISEASE PHENOTYPE CAUSED BY A NOVEL CANONICAL SPLICE-SITE MUTATION

DEMİR K., Zou M., Al-Rijjal R. A., BinEssa H., Acar S., Durmaz E., et al.

ENDOCRINE PRACTICE , cilt.26, sa.1, ss.72-81, 2020 (SCI-Expanded)

Characteristics of Turkish children with Type 2 diabetes at onset: a multicentre, cross-sectional study

Hatun S., Mutlu G. Y., Cinaz P., DEMİRCİOĞLU S., Ekberzade A., BEREKET A., et al.

DIABETIC MEDICINE , cilt.36, sa.10, ss.1243-1250, 2019 (SCI-Expanded)

Elevated anti-tissue transglutaminase antibodies in children newly diagnosed with type 1 diabetes do not always indicate celiac disease

Paketci A., Armagan C., ERBAŞ İ. M., DEMİR K., ABACI A., BÖBER E.

HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.141, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma

A Rare Cause of Hypogonadotropic Hypogonadism: FGFR1Mutation

ERBAŞ İ. M., Paketci A., Acar S., Kotan D., DEMİR K., ABACI A., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.587, 2019 (SCI-Expanded)

Evaluation of Clinical, Demographic Data and Treatment Results of Cases with Graves' Disease

Sonmez A. A., ERBAŞ İ. M., Paketci A., Acar S., DEMİR K., BÖBER E., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.610-611, 2019 (SCI-Expanded)

Evaluation of Thyroid Function Tests in Children with Chronic Liver Diseases

On S. S., Acar S., DEMİR K., ABACI A., ÖZTÜRK Y., Celik S. K., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.271, 2019 (SCI-Expanded)

Papillary Thyroid Cancer Associated With Hyperthyroidism

Acar S., Paketci A., DEMİR K., ATEŞ O., ÖZER E., ÖZDOĞAN Ö., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.91, ss.493, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma

Comparison of Treatment Regimens in Management of Severe Hypercalcemia Due to Vitamin D Intoxication in Children

DEMİR K., DÖNERAY H., Kara C., Atay Z., Cetinkaya S., Cayir A., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.11, sa.2, ss.140-148, 2019 (SCI-Expanded)

A toddler with a novel LEPR mutation

Armagan C., Yilmaz C., Koc A., Abacı A., Ülgenalp A., Böber E., et al.

HORMONES-INTERNATIONAL JOURNAL OF ENDOCRINOLOGY AND METABOLISM , cilt.18, sa.2, ss.237-240, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma

Long-term monitoring of Graves' disease in children and adolescents: a single-center experience

Tunc S., Koprulu O., Ortac H., Nalbantoglu O., Dizdarer C., DEMİR K., et al.

TURKISH JOURNAL OF MEDICAL SCIENCES , cilt.49, sa.2, ss.464-471, 2019 (SCI-Expanded)

Presentation of central precocious puberty in two patients with Tay-Sachs disease

Acar S., ARSLAN N., Paketci A., Okur T. D., DEMİR K., BÖBER E., et al.

HORMONES-INTERNATIONAL JOURNAL OF ENDOCRINOLOGY AND METABOLISM , cilt.17, sa.3, ss.415-418, 2018 (SCI-Expanded)

Comparison of the effects of the l-dopa and insulin tolerance tests on cortisol secretion

Acar S., Paketci A., Tuhan H., DEMİR K., Bober E., ABACI A.

JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , cilt.41, sa.8, ss.901-907, 2018 (SCI-Expanded)

Positive correlation of galanin with insulin resistance and triglyceride levels in obese children

Acar S., Paketci A., KÜME T., DEMİR K., Gursoy Calan Ö., BÖBER E., et al.

Turkish journal of medical sciences , cilt.48, sa.3, ss.560-568, 2018 (SCI-Expanded)

Graves' disease following allogenic hematopoietic stem cell transplantation for severe aplastic anemia: case report and literature review

Paketci A., DEMİR K., TÜFEKÇİ Ö., Acar S., ABACI A., YILMAZ Ş., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.31, sa.5, ss.589-593, 2018 (SCI-Expanded)

Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3

Acar S., Bin Essai H. A., DEMİR K., Al-Rijjal R. A., Zou M., ÇATLI G., et al.

PLOS ONE , cilt.13, sa.3, 2018 (SCI-Expanded)

Increased concentrations of serum nesfatin-1 levels in childhood with idiopathic chronic malnutrition

Acar S., ÇATLI G., KÜME T., Tuhan H., Gursoy Calan Ö., DEMİR K., et al.

TURKISH JOURNAL OF MEDICAL SCIENCES , cilt.48, sa.2, ss.378-385, 2018 (SCI-Expanded) Sürdürülebilir Kalkınma

Growth Hormone Deficiency Due to Whole-gene Deletion of GHRHR

Acar S., DEMİR K., Kirbiyik O., Paketci A., Erdogan K. M., ABACI A., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.90, ss.380, 2018 (SCI-Expanded)

Galanin is Positively Correlated with Insulin Resistance and Triglyceride Levels in Obese Children

Acar S., Paketci A., KÜME T., DEMİR K., Calan O. G., BÖBER E., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.90, ss.319, 2018 (SCI-Expanded)

Long Term Monitoring of Graves Disease in Children and Adolescents: Single Center Experience

Tunc S., Koprulu O., Ortac H., Nalbantoglu O., Dizdarer C., DEMİR K., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.90, ss.604, 2018 (SCI-Expanded)

Nationwide Hypophosphatemic Rickets Study

ŞIKLAR Z., DEMİRCİOĞLU S., BEREKET A., ABACI A., BAŞ F., DEMİR K., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.90, ss.109-110, 2018 (SCI-Expanded)

Comprehensive Genetic Testing Shows One in Five Children with Diabetes and Non-Autoimmune Extra-Pancreatic Features Have Monogenic Aetiology

Patel K. A., Colclough K., Ozbek M. N., Yildiz M., GÜRAN T., Kocyigit C., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.90, ss.213, 2018 (SCI-Expanded) Sürdürülebilir Kalkınma

Serum Level of Biotin Rather Than the Daily Dose Is the Main Determinant of the Interference on Thyroid Function Assays in Patients with Biotinidase Deficiency

Paketci A., Kose E., Calan Ö., Acar S., Teke P., Demirci F., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.90, ss.613, 2018 (SCI-Expanded)

A Novel Compound Heterozygous Mutation in CYP19A1 Resulting in Aromatase Deficiency with Normal Gonadotropin Levels and Ovarian Tissue

Acar S., Paketci A., Onay H., ÇANKAYA T., Gursoy S., ÖZHAN B., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.90, ss.588-589, 2018 (SCI-Expanded)

Clinical Heterogeneity and Phenotypic Expansion of NaPi-IIa-Associated Disease

DEMİR K., Yildiz M., Bahat H., Goldman M., Hassan N., Tzur S., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , cilt.102, sa.12, ss.4604-4614, 2017 (SCI-Expanded)

A Mutation in INSR in a Child Presenting with Severe Acanthosis Nigricans

Tuhan H., Ceylaner S., Nalbantoglu O., Acar S., ABACI A., BÖBER E., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.9, sa.4, ss.371-374, 2017 (SCI-Expanded)

Genetic Causes of Rickets

Acar S., DEMİR K., Shi Y.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.9, ss.88-105, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma

Increased circulating interleukin-8 in patients with resistance to thyroid hormone receptor alpha

van der Spek A. H., Surovtseva O. V., Aan S., Tool A. T. J., van de Geer A., DEMİR K., et al.

ENDOCRINE CONNECTIONS , cilt.6, sa.8, ss.731-740, 2017 (SCI-Expanded)

Serum galectin-1 levels are positively correlated with body fat and negatively with fasting glucose in obese children.

Acar S., Paketci A., KÜME T., Tuhan H., Calan Ö., DEMİR K., et al.

Peptides , cilt.95, ss.51-56, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma

Anemia in Patients With Resistance to Thyroid Hormone alpha: A Role for Thyroid Hormone Receptor a in Human Erythropoiesis

van Gucht A. L. M., Meima M. E., Moran C., Agostini M., Tylki-Szymanska A., Krajewska-Walasek M., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , cilt.102, sa.9, ss.3517-3525, 2017 (SCI-Expanded)

Identification of an AR mutation in Klinefelter syndrome during evaluation for penoscrotal hypospadias

Acar S., Tuhan H., BORA E., DEMİR K., Onay H., Ercal D., et al.

HORMONES-INTERNATIONAL JOURNAL OF ENDOCRINOLOGY AND METABOLISM , cilt.16, sa.3, ss.313-317, 2017 (SCI-Expanded)

Infantile-onset thiamine responsive megaloblastic anemia syndrome with SLC19A2 mutation: a case report

Katipoglu N., Karapinar T. H., DEMİR K., Koker S. A., Nalbantoglu O., Ay Y., et al.

ARCHIVOS ARGENTINOS DE PEDIATRIA , cilt.115, sa.3, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma

Higher-Than-Conventional Subcutaneous Regular Insulin Doses in Diabetic Ketoacidosis in Children and Adolescents

Bag O., Tunc S., Nalbantoglu O., Ecevit C., Ozturk A., Ozkan B., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.9, sa.2, ss.132-137, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma

A Comprehensive Online Calculator for Pediatric Endocrinologists: CEDD Cozuum/TPEDS Metrics

DEMİR K., ÖZEN S., KONAKÇI E., Aydin M., Darendeliler F.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.9, sa.2, ss.182-184, 2017 (SCI-Expanded)

Neurodevelopmental Outcome of Children with Congenital Hypothyroidism Diagnosed in a National Screening Program in Turkey

Baysal B. T., Baysal B., Genel F., Erdur B., Ozbek E., DEMİR K., et al.

INDIAN PEDIATRICS , cilt.54, sa.5, ss.381-384, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma

Changes of thyroid hormonal status in patients receiving ketogenic diet due to intractable epilepsy

Kose E., Guzel O., DEMİR K., ARSLAN N.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.30, sa.4, ss.411-416, 2017 (SCI-Expanded)

CLINICAL CHARACTERISTICS OF TURKISH CHILDREN AND ADOLESCENTS WITH TYPE 2 DIABETES

Hatun S., Mutlu G. Y., CİNAZ P., Erbas M. Y., Akcay T., Onal H., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.88, ss.282, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma

THE RELATION OF SERUM GALECTIN-1 LEVEL WITH CLINICAL AND METABOLIC PARAMETERS IN OBESE CHILDREN

Acar S., Paketci A., KÜME T., Tuhan H. U., Calan O. G., DEMİR K., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.88, ss.319, 2017 (SCI-Expanded)

COMPARISON OF THE EFFECTS OF L-DOPA AND INSULIN TOLERANCE TESTS ON CORTISOL SECRETION

Acar S., Paketci A., Tuhan H. U., DEMİR K., BÖBER E., ABACI A.

HORMONE RESEARCH IN PAEDIATRICS , cilt.88, ss.109-110, 2017 (SCI-Expanded)

A novel splice site mutation of FGD1 gene in an Aarskog-Scott syndrome patient with a large anterior fontanel

PARILTAY E., Hazan F., Ataman E., DEMİR K., Etlik O., Ozbek E., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.29, sa.9, ss.1111-1114, 2016 (SCI-Expanded)

Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor-alpha Mutations

DEMİR K., van Gucht A. L. M., Buyukinan M., Catli G., AYHAN Y., Bas V. N., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , cilt.101, sa.8, ss.2945-2954, 2016 (SCI-Expanded)

Anti-cyclic citrullinated peptide antibodies are not frequently observed in children with type 1 diabetes mellitus: a single-center study

Yildiz M., Isleten F., DEMİR K., Celik N., Korkmaz H. A., Tuglu B., et al.

TURKISH JOURNAL OF PEDIATRICS , cilt.58, sa.4, ss.395-399, 2016 (SCI-Expanded) Sürdürülebilir Kalkınma

Association of Wolfram syndrome with Fallot tetralogy in a girl

Korkmaz H. A., DEMİR K., Hazan F., Yildiz M., Elmas O. N., Ozkan B.

ARCHIVOS ARGENTINOS DE PEDIATRIA , cilt.114, sa.3, 2016 (SCI-Expanded) Sürdürülebilir Kalkınma

Relationship between oxidative stress and blood glucose fluctuations evaluated with daily glucose monitoring in children with type 1 diabetes mellitus

Altincik A., Tuglu B., DEMİR K., Catli G., ABACI A., BÖBER E.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.29, sa.4, ss.435-439, 2016 (SCI-Expanded) Sürdürülebilir Kalkınma

Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome

Sari E., BEREKET A., Yesilkaya E., BAŞ F., Bundak R., Aydin B. K., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A , cilt.170, sa.4, ss.942-948, 2016 (SCI-Expanded)

Levothyroxine replacement in primary congenital hypothyroidism: the higher the initial dose the higher the rate of overtreatment

Tuhan H., ABACI A., Cicek G., Anik A., Catli G., DEMİR K., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.29, sa.2, ss.133-138, 2016 (SCI-Expanded) Sürdürülebilir Kalkınma

Can ambulatory blood pressure monitoring detect early diastolic dysfunction in children with type 1 diabetes mellitus: correlations with B-type natriuretic peptide and tissue Doppler findings

KIR M., ÇETİN B. Ş., DEMİR K., Yilmaz N., Kizilca O., Demircan T., et al.

PEDIATRIC DIABETES , sa.1, ss.21-27, 2016 (SCI-Expanded) Sürdürülebilir Kalkınma

Retrospective Evaluation of the Efficiency of Metformin Therapy in Obese Children with Insulin Resistance

Cicek G., ABACI A., Tuhan H., DEMİR K., BÖBER E.

HORMONE RESEARCH IN PAEDIATRICS , cilt.86, ss.337, 2016 (SCI-Expanded)

Higher-Than-Conventional Subcutaneous Regular Insulin Doses Following Diabetic Ketoacidosis are Associated with Better Short-term Glycemic Control

Bag O., Tunc S., Nalbantoglu O., Ecevit C., Ozturk A., Ozkan B., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.86, ss.216-217, 2016 (SCI-Expanded) Sürdürülebilir Kalkınma

Spectrum of the Genetic Defects in Hypophosphatemic Rickets in A Group of Turkish Children

Acar S., Al-Rijjal R. A., DEMİR K., Kattan W. E., ÇATLI G., BinEssa H., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.86, ss.173, 2016 (SCI-Expanded)

Complete Idiopathic Hypogonadotropic Hypogonadism due to Homozygous GNRH1 Mutations in the Mutational Hot Spots in the Region Encoding the Decapeptide

Mengen E., Tunc S., KOTAN L. D., Nalbantoglu O., DEMİR K., GÜRBÜZ F., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.85, sa.2, ss.107-111, 2016 (SCI-Expanded)

Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort

GÜRAN T., Buonocore F., Saka N., Ozbek M. N., Aycan Z., BEREKET A., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , cilt.101, sa.1, ss.283-291, 2016 (SCI-Expanded)

Melanocortin-4 Receptor Gene Mutations in a Group of Turkish Obese Children and Adolescents

Tunc S., DEMİR K., Tukun F. A., Topal C., Hazan F., Saglam B., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.86, ss.320-321, 2016 (SCI-Expanded)

Identification of an AR Mutation in Klinefelter's Syndrome during Evaluation for Penoscrotal Hypospadias

Acar S., Tuhan H., BORA E., DEMİR K., Onay H., Ercal D., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.86, ss.279, 2016 (SCI-Expanded)

Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Osteopetrosis of Infancy

DEMİR K., Nalbantoglu O., Karaer K., Korkmaz H. A., Yildiz M., Tunc S., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.7, sa.4, ss.356-357, 2015 (SCI-Expanded)

A novel mutation of AMH in three siblings with persistent Mullerian duct syndrome

Nalbantoglu O., DEMİR K., Korkmaz H. A., Buyukinan M., Yildiz M., Tunc S., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.28, sa.11-12, ss.1379-1382, 2015 (SCI-Expanded)

Molecular diagnosis of maturity-onset diabetes of the young (MODY) in Turkish children by using targeted next-generation sequencing

Anik A., Catli G., ABACI A., Sari E., Yesilkaya E., Korkmaz H. A., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.28, ss.1265-1271, 2015 (SCI-Expanded) Sürdürülebilir Kalkınma

The Missense Alteration A5T of the Thyroid Peroxidase Gene is Pathogenic and Associated with Mild Congenital Hypothyroidism

CANGÜL H., DEMİR K., Babayigit H. O., ABACI A., BÖBER E.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.7, sa.3, ss.238-241, 2015 (SCI-Expanded)

The Role of Thyrotropin-Releasing Hormone Stimulation Test in Management of Hyperthyrotropinemia in Infants

Altincik A., DEMİR K., Catli G., ABACI A., BÖBER E.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.7, sa.3, ss.211-216, 2015 (SCI-Expanded)

Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group

Darendeliler F., Yesilkaya E., BEREKET A., BAŞ F., Bundak R., Sari E., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.7, sa.3, ss.183-191, 2015 (SCI-Expanded)

Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1A

DEMİR K., Kattan W. E., Zou M., Durmaz E., BinEssa H., Nalbantoglu O., et al.

PLOS ONE , cilt.10, sa.7, 2015 (SCI-Expanded)

Two different patterns of mini- puberty in two 46,XY newborns with 17 beta- hydroxysteroid dehydrogenase type 3 deficiency

DEMİR K., Yildiz M., Elmas O. N., Korkmaz H. A., Tunc S., Olukman O., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.28, sa.7-8, ss.961-965, 2015 (SCI-Expanded)

Normosmic idiopathic hypogonadotropic hypogonadism due to a novel homozygous nonsense c.C969A (p.Y323X) mutation in the KISS1R gene in three unrelated families

Demirbilek H., Ozbek M. N., DEMİR K., KOTAN L. D., Cesur Y., Doğan M., et al.

CLINICAL ENDOCRINOLOGY , cilt.82, sa.3, ss.429-438, 2015 (SCI-Expanded)

Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome

Walz K., Cohen D., Neilsen P. M., Foster J., Brancati F., DEMİR K., et al.

HUMAN GENETICS , cilt.134, sa.2, ss.181-190, 2015 (SCI-Expanded)

GPR30 Gene Polymorphisms Are Associated with Gynecomastia Risk in Adolescents

Korkmaz H. A., EDGÜNLÜ T., Eren E., DEMİR K., Cakir E. D. P., Celik S. K., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.83, sa.3, ss.177-182, 2015 (SCI-Expanded) Sürdürülebilir Kalkınma

Turner syndrome and associated problems in turkish children: A multicenter study

Yeşilkaya E., BEREKET A., Darendeliler F., BAŞ F., POYRAZOĞLU Ş., Aydın B. K., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.7, sa.1, ss.27-36, 2015 (SCI-Expanded) Sürdürülebilir Kalkınma

Obesity and Insulin Resistance after Chemotherapy in Patients with Acute Lymphoblastic Leukemia

Oymak Y., Uysal B., Karapinar T. H., Ay Y., İNCE D., Demirag B., et al.

BLOOD , cilt.124, sa.21, 2014 (SCI-Expanded) Sürdürülebilir Kalkınma

Importance of Insulin Immunoassays in the Diagnosis of Factitious Hypoglycemia

Elmas O. N., DEMİR K., Soylu N., Celik N., Ozkan B.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.6, sa.4, ss.258-261, 2014 (SCI-Expanded) Sürdürülebilir Kalkınma

Management of central diabetes insipidus with oral desmopressin lyophilisate in infants

Korkmaz H. A., DEMİR K., Kilic F. K., TEREK D., Arslanoglu S., Dizdarer C., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.27, sa.9-10, ss.923-927, 2014 (SCI-Expanded) Sürdürülebilir Kalkınma

Autoimmune thyroiditis in children and adolescents with type 1 diabetes mellitus is associated with elevated IgG4 but not with low vitamin D

DEMİR K., KESKİN M., Kor Y., Karaoglan M., Bulbul O. G.

HORMONES-INTERNATIONAL JOURNAL OF ENDOCRINOLOGY AND METABOLISM , cilt.13, sa.3, ss.361-368, 2014 (SCI-Expanded) Sürdürülebilir Kalkınma

Genetic variants of estrogen beta and leptin receptors may cause gynecomastia in adolescent

Eren E., EDGÜNLÜ T., Korkmaz H. A., Cakir E. D. P., DEMİR K., ÇETİN E. S., et al.

GENE , cilt.541, sa.2, ss.101-106, 2014 (SCI-Expanded)

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 , cilt.82, sa.4, ss.261-271, 2014 (SCI-Expanded)

Acceleration of Puberty During Growth Hormone Therapy in a Child with Septo-Optic Dysplasia

Catli G., Altincik A., Anik A., DEMİR K., GÜLERYÜZ UÇAR H., ABACI A., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.6, sa.2, ss.116-118, 2014 (SCI-Expanded)

Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community

Cangul H., Aycan Z., Olivera-Nappa A., SAĞLAM H., Schoenmakers N. A., Boelaert K., et al.

CLINICAL ENDOCRINOLOGY , cilt.79, sa.2, ss.275-281, 2013 (SCI-Expanded)

Monitoring and prognostic evaluation of patients with congenital hypothyroidism treated in a pediatric endocrinology unit

Unuvar T., DEMİR K., ABACI A., Atas A., Buyukgebiz A., BÖBER E.

TURKISH JOURNAL OF PEDIATRICS , cilt.55, sa.4, ss.384-390, 2013 (SCI-Expanded)

A novel mutation in a mother and a son with Aarskog-Scott syndrome

Altincik A., Kaname T., DEMİR K., BÖBER E.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.26, ss.385-388, 2013 (SCI-Expanded)

Severe short stature due to 3-M syndrome with a novel OBSL1 gene mutation

DEMİR K., Altincik A., BÖBER E.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.26, ss.147-150, 2013 (SCI-Expanded)

The Role of Initial Clinical and Laboratory Findings in Infants With Hyperthyrotropinemia to Predict Transient or Permanent Hypothyroidism

Unuvar T., DEMİR K., ABACI A., Buyukgebiz A., BÖBER E.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.5, sa.3, ss.170-173, 2013 (SCI-Expanded) Sürdürülebilir Kalkınma

Diabetes Care, Glycemic Control, Complications, and Concomitant Autoimmune Diseases in Children with Type 1 Diabetes in Turkey: A Multicenter Study

Simsek D. G., Aycan Z., ÖZEN S., Cetinkaya S., Kara C., ABALI S., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , cilt.5, sa.1, ss.20-26, 2013 (SCI-Expanded) Sürdürülebilir Kalkınma

Vitamin D Dependent Rickets Type I: Two Cases Report

Ulusoy E., DEMİR K., Altincik A., Catli G., ABACI A., Bekem Soylu O., et al.

TURKIYE KLINIKLERI TIP BILIMLERI DERGISI , cilt.32, sa.6, ss.1786-1790, 2012 (SCI-Expanded) Sürdürülebilir Kalkınma

Hyperprolactinemia in children: clinical features and long-term results

Catli G., ABACI A., Altincik A., DEMİR K., Can S., Buyukgebiz A., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.25, ss.1123-1128, 2012 (SCI-Expanded) Sürdürülebilir Kalkınma

Concurrent protracted febrile myalgia syndrome in a child with diabetic ketoacidosis

DEMİR K., ÇARMAN K. B., Kasap B.

PEDIATRIC DIABETES , cilt.13, sa.6, ss.510-513, 2012 (SCI-Expanded) Sürdürülebilir Kalkınma

Bilateral pheochromocytoma as first manifestation of von Hippel-Lindau disease: a case report

Catli G., ABACI A., Neumann H. C. H., Altincik A., DEMİR K., BÖBER E.

TURKISH JOURNAL OF PEDIATRICS , cilt.54, sa.5, ss.532-535, 2012 (SCI-Expanded)

Clinical profile and etiologies of children with central diabetes insipidus: a single-center experience from Turkey

Catli G., ABACI A., DEMİR K., Ulusoy E., Altincik A., Buyukgebiz A., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.25, sa.5-6, ss.499-502, 2012 (SCI-Expanded) Sürdürülebilir Kalkınma

Evaluation of neutrophil gelatinase-associated lipocalin in normoalbuminuric normotensive type 1 diabetic adolescents

DEMİR K., ABACI A., KÜME T., Altincik A., Catli G., BÖBER E.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.25, ss.517-523, 2012 (SCI-Expanded) Sürdürülebilir Kalkınma

TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis

Cangul H., Aycan Z., SAĞLAM H., Forman J. R., Cetinkaya S., TARIM Ö. F., et al.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.25, ss.419-426, 2012 (SCI-Expanded)

The Exon 3-Deleted/Full-Length Growth Hormone Receptor Polymorphism and Response to Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome: A Multicenter Study

BAŞ F., Darendeliler F., Aycan Z., Cetinkaya E., BERBEROĞLU M., ŞIKLAR Z., et al.

HORMONE RESEARCH IN PAEDIATRICS , cilt.77, sa.2, ss.85-93, 2012 (SCI-Expanded)

A mother and son with Noonan syndrome resulting from a PTPN11 mutation Reply

BÖBER E., DEMİR K.

TURKISH JOURNAL OF PEDIATRICS , cilt.53, sa.1, ss.118, 2011 (SCI-Expanded)

Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidism

Cangul H., Morgan N. V., Forman J. R., SAĞLAM H., Aycan Z., Yakut T., et al.

CLINICAL ENDOCRINOLOGY , cilt.73, sa.5, ss.671-677, 2010 (SCI-Expanded)

Tamoxifen as First-line Treatment in a Premenarchal Girl with Juvenile Breast Hypertrophy

DEMİR K., Unuvar T., Eren S., ABACI A., BÖBER E.

Journal of Pediatric and Adolescent Gynecology , cilt.23, sa.5, 2010 (SCI-Expanded)

A 2-year-old Boy with a Testicular Mass

Unuvar T., DEMİR K., ABACI A., Atas A., Cakmakci H., BÖBER E.

PEDIATRIC ANNALS , cilt.39, sa.8, ss.471-474, 2010 (SCI-Expanded)

Growth of children with type 1 diabetes mellitus

DEMİR K., Altincik A., Abaci A., Büyükgebiz A., BÖBER E.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.2, sa.2, ss.72-77, 2010 (SCI-Expanded) Sürdürülebilir Kalkınma

Fine-needle aspiration biopsy in the diagnosis and follow-up of thyroid nodules in childhood

Altincik A., DEMİR K., Abaci A., BÖBER E., Büyügebiz A.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.2, sa.2, ss.78-80, 2010 (SCI-Expanded)

A mother and son with Noonan syndrome resulting from a PTPN11 mutation: first report of molecularly proven cases from Turkey

DEMİR K., Yntema H. G., Altincik A., BÖBER E.

TURKISH JOURNAL OF PEDIATRICS , cilt.52, sa.3, ss.321-324, 2010 (SCI-Expanded)

A NOVEL MUTATION IN THE AVPR2 GENE (222delA) ASSOCIATED WITH X-LINKED NEPHROGENIC DIABETES INSIPIDUS IN A BOY WITH GROWTH FAILURE

ABACI A., Wood K., DEMİR K., Buyukgebiz A., BÖBER E., Kopp P.

ENDOCRINE PRACTICE , cilt.16, sa.2, ss.231-236, 2010 (SCI-Expanded) Sürdürülebilir Kalkınma

Metabolic Alterations During Valproic Acid Treatment: A Prospective Study

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

PEDIATRIC NEUROLOGY , cilt.41, sa.6, ss.435-439, 2009 (SCI-Expanded) Sürdürülebilir Kalkınma

A Comparison of Multiple Daily Insulin Therapy with Continuous Subcutaneous Insulin Infusion Therapy in Adolescents with Type 1 Diabetes Mellitus: A Single-Center Experience From Turkey

ABACI A., Atas A., Unuvar T., DEMİR K., BÖBER E., Buyukgebiz A.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.22, sa.6, ss.539-545, 2009 (SCI-Expanded) Sürdürülebilir Kalkınma

Endocrine disrupters - With special emphasis on sexual development

Abaci A., DEMİR K., BÖBER E., Buyukgebiz A.

Pediatric Endocrinology Reviews , cilt.6, sa.4, ss.464-475, 2009 (SCI-Expanded) Sürdürülebilir Kalkınma

Mutation analysis of a mother and son with Noonan syndrome: first report from Turkey

DEMİR K., Ijntema H., Altincik A., BÖBER E.

HORMONE RESEARCH , cilt.72, ss.499, 2009 (SCI-Expanded)

Evaluation of the effect of type 1 diabetes mellitus on the auxological data of children

DEMİR K., Altincik A., ABACI A., BÖBER E., Buyukgebiz A.

HORMONE RESEARCH , cilt.72, ss.178, 2009 (SCI-Expanded) Sürdürülebilir Kalkınma

Favourable outcome with tamoxifen in juvenile breast hypertrophy

DEMİR K., Unuvar T., Eren S., ABACI A., BÖBER E.

HORMONE RESEARCH , cilt.72, ss.493, 2009 (SCI-Expanded)

Clarithromycin, montelukast, and pentoxifylline combination treatment ameliorates experimental neonatal hyperoxic lung injury

DEMİR K., KUMRAL A., DUMAN N., SARIOĞLU S., Yilmaz O., Yesilirmak D. C., et al.

JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE , cilt.21, sa.6, ss.407-413, 2008 (SCI-Expanded)

A non-endocrine cause of testicular enlargement mimicking precocious puberty: Testicular microlithiasis

BÖBER E., Dundar B., DEMİR K., ABACI A., Cakmakci H., Buyukgebiz A.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , cilt.20, sa.11, ss.1237-1240, 2007 (SCI-Expanded)

Predictive value of clinical and laboratory variables for vesicoureteral reflux in children

SOYLU A., Kasap B., DEMİR K., Turkmen M., Kavukcu S.

PEDIATRIC NEPHROLOGY , cilt.22, sa.6, ss.844-848, 2007 (SCI-Expanded) Sürdürülebilir Kalkınma

Chemical burn in domestic setting with an uncommon agent: hydrofluoric acid

DEMİR K., Ozdemir D., Topcu A., Duman M., Vayvada H.

EUROPEAN JOURNAL OF EMERGENCY MEDICINE , cilt.14, sa.2, ss.106-107, 2007 (SCI-Expanded)

Corneal involvement in Papillon-Lefevre syndrome

Saatci P., Arli A., DEMİR K., Saatci A., Kavakcu S.

JOURNAL OF PEDIATRIC OPHTHALMOLOGY & STRABISMUS , cilt.43, sa.3, ss.167-169, 2006 (SCI-Expanded)

Corneal involvement in Papillon-Lefèvre syndrome

Saatci P., Arli A. Ö., DEMİR K., SAATCİ A. O., Kavakçu S.

Journal of Pediatric Ophthalmology and Strabismus , cilt.43, sa.3, ss.167-169, 2006 (SCI-Expanded)

Multisystemic leukocytoclastic vasculitis affecting the central nervous system

Soylu A., Kavukcu S., Erdur B., DEMİR K., Turkmen M.

PEDIATRIC NEUROLOGY , cilt.33, sa.4, ss.289-291, 2005 (SCI-Expanded)

Sigmoid sinus thrombosis following mastoiditis - Early diagnosis enhances good prognosis

Ozdemir D., Cakmakci H., Ikiz A., DEMİR K., Yilmaz S., Dirik E., et al.

PEDIATRIC EMERGENCY CARE , cilt.21, sa.9, ss.606-609, 2005 (SCI-Expanded)

A case of Takayasu disease with findings of incomplete Alagille syndrome

Kavukcu S., DEMİR K., SOYLU A., Anal O., Saatci O., Goktay Y.

RHEUMATOLOGY INTERNATIONAL , cilt.25, sa.7, ss.555-557, 2005 (SCI-Expanded)

Spontaneous intestinal perforation after oral ibuprofen treatment of patent ductus arteriosus in two very-low-birthweight infants

Tatli M., Kumral A., Duman N., DEMİR K., Gurcu O., ÖZKAN H.

ACTA PAEDIATRICA , cilt.93, sa.7, ss.999-1001, 2004 (SCI-Expanded)

Diğer Dergilerde Yayınlanan Makaleler

Interpretation, differential diagnosis, and clinical implications of abnormal thyroid function tests in children

Kağızmanlı G. A., DEMİR K.

Trends in Pediatrics , cilt.4, sa.2, ss.61-71, 2023 (Scopus)

Çocuk ve Adolesanlarda Halsizlik ve Kilo Kaybı Durumunda Akla Gelmesi Gereken Bir Hastalık: Adrenal Yetmezlik

ARMAĞAN C., PAKETÇİ A., ACAR S., AKÇURA Y. D., ERBAŞ İ. M., ABACI A., et al.

Turkish Journal of Pediatric Disease , cilt.15, sa.4, ss.337-340, 2021 (Hakemli Dergi)

Konjenital Hiperinsülinemik Hipoglisemi Tanılı HastalardaKlinik ve Genetik Özellikler ile Tedavi Sonuçları: TekMerkez Deneyimi

ERBAŞ İ. M., ÇATLI G., PAKETÇİ A., ANIK A., DEMİR K., BÖBER E., et al.

Güncel Pediatri , cilt.18, sa.3, ss.317-335, 2020 (ESCI)

Clinical, Genetic Features and Treatment Results in Patients with Congenital Hyperinsulinemic Hypoglycemia: A Single Center Experience

ERBAŞ İ. M., Catli G., Paketci A., ANIK A., DEMİR K., BÖBER E., et al.

GUNCEL PEDIATRI-JOURNAL OF CURRENT PEDIATRICS , cilt.18, sa.3, ss.317-335, 2020 (ESCI)

Doğumsal Hipotiroidi ile Ebeveyn Yaşı İlişkisi

ÜNVER TUHAN H., ERKOYUN E., ACAR S., ABACI A., BÖBER E., DEMİR K.

Türkiye Çocuk Hastalıkları Dergisi , cilt.13, sa.6, ss.451-455, 2019 (Hakemli Dergi)

Comparison of the Efficacy of Daily and Weekly Oral Alendronate Treatment in Patients with Secondary Osteoporosis

Acar S., Paketci A., DEMİR K., BÖBER E., ABACI A.

IZMIR DR BEHCET UZ COCUK HASTANESI DERGISI , cilt.9, sa.3, ss.191-198, 2019 (ESCI)

Hemanjiyom İçin Propranolol Tedavisi Alan Bir İnfantta Gelişen Semptomatik Hipoglisemi: Olgu Raporu ve Önlemler

PAKETÇİ A., DEMİR K., ACAR S., ABACI A., BÖBER E.

Zeynep Kamil Tıp Bülteni , 2018 (Hakemli Dergi)

A Novel De Novo Missense Mutation in HNF4A Resulting in Sulfonylurea-Responsive Maturity-onset Diabetes of the Young

Acar S., ABACI A., DEMİR K., Ozdemir T. R., Ozyilmaz B., BÖBER E.

JOURNAL OF PEDIATRIC RESEARCH , cilt.5, sa.3, ss.156-160, 2018 (ESCI) Sürdürülebilir Kalkınma

Gebelikte tiroid hastalıklarının neonatal etkileri ve TSH yüksekliği olan bebeğe yaklaşım: Türk Neonatoloji ve Çocuk Endokrinoloji ve Diabet Dernekleri Uzlaşı Raporu

ÖZÖN Z. A., TEKİN A. N., ŞIKLAR Z., KARA C., GÜLCAN H., TAŞTEKİN A., et al.

Türk Pediatri Arşivi , cilt.53, ss.209-223, 2018 (Scopus) Sürdürülebilir Kalkınma

Early-Onset Isolated Bilateral Pheochromocytoma As a Major Clinical Manifestation of von-Hippel Lindau Syndrome Type 2C

Acar S., Tuhan H., DEMİR K., AYKUT A., DURMAZ A., Karaarslan U. U., et al.

JOURNAL OF PEDIATRIC RESEARCH , cilt.5, sa.1, ss.48-51, 2018 (ESCI) Sürdürülebilir Kalkınma

Neonatal effects of thyroid diseases in pregnancy and approach to the infant with increased TSH: Turkish Neonatal and Pediatric Endocrinology and Diabetes Societies consensus report

ÖZÖN Z. A., TEKİN N., ŞIKLAR Z., Gulcan H., Kara C., TAŞTEKİN A., et al.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , cilt.53, 2018 (ESCI)

Turning over a new page in the national neonatal endocrinological approach

ERDEVE Ö., DEMİR K., KOÇ E., Darendeliler F.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , cilt.53, 2018 (ESCI)

Evaluation of Demographic, Clinical and Laboratory Features of Cases with Type 1 Diabetes Mellitus at Diagnosis

ACAR S., PAKETÇİ A., GÖREN Y., ÇATLI G., ANIK A., ÜNVER TUHAN H., et al.

Turkish Journal of Pediatric Disease , 2017 (Hakemli Dergi) Sürdürülebilir Kalkınma

Changes in the Frequency of Diabetic Ketoacidosis in Type I Diabetes Mellitus Cases at Diagnosis: A Fifteen-Year Single Center Experience

Acar S., Goren Y., Paketci A., Anik A., Catli G., Tuhan H., et al.

JOURNAL OF PEDIATRIC RESEARCH , cilt.4, sa.3, ss.143-148, 2017 (ESCI) Sürdürülebilir Kalkınma

Tip 1 Diyabetes Mellitus Olgularının Tanı Anındaki Demografik,Klinik ve Laboratuvar Özelliklerinin Değerlendirilmesi

ACAR S., PAKETÇİ A., GÖREN Y., ÇATLI G., ANIK A., ÜNVER TUHAN H., et al.

TÜRKİYE ÇOCUK HASTALIKLARI DERGİSİ , 2017 (Hakemli Dergi) Sürdürülebilir Kalkınma

A rare cause of a 46, XY disorders of sex development: Persistent mullerian duct syndrome

Acar S., Paketci A., Onay H., DEMİR K., ATEŞ O., BÖBER E., et al.

IZMIR DR BEHCET UZ COCUK HASTANESI DERGISI , cilt.7, sa.3, ss.242-246, 2017 (ESCI)

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

İzole Büyüme Hormonu Eksikliği Nedeniyle Büyüme Hormonu Tedavisi Alan Olguların Klinik Özelliklerinin Değerlendirilmesi

Ersoy S., Besci Ö., Yüksek Acinikli K., Akın Kağızmanlı G., Demir K., Böber E., et al.

67. Türkiye Milli Pediatri Kongresi, Girne, Kıbrıs (Kktc), 18 - 22 Ekim 2023, ss.1 Sürdürülebilir Kalkınma

Aromatase inhibitors: an effective and safe option for height increment in boys with growth hormone deficiency?

Akın Kağızmanlı G., Özalp Kızılay D., Besci Ö., Yüksek Acinikli K., Özen S., Demir K., et al.

61st Annual ESPE (ESPE 2023), The Hague, Hollanda, 21 - 23 Eylül 2023, ss.89

Psychosocial Evaluation of Girls with Rapidly Progressive Puberty Presenting with Early Menarche

Yüksek Acinikli K., Besci Ö., Akın Kağızmanlı G., Gündoğan N., Unutmaz G., Esen A. B., et al.

61st Annual ESPE (ESPE 2023), The Hague, Hollanda, 21 - 23 Eylül 2023, ss.95

Doğumsal hipotiroidi Ulusal Tarama Programından bir kesit; son 6 yıl değerlendirimi, tiroksin dozu geçici/kalıcı doğumsal hipotiroidi öngörümünde yol gösterici olabilir

Anık A., Sayılı U., Tercan U., Buhur Pirimoğlu M., Dündar İ., Singin B., et al.

26. Ulusal Pediatrik Endokrin ve Diyabet Kongresi, Antalya, Türkiye, 26 - 30 Ekim 2022, ss.54

Santral Erken Puberte veya Hızlı İlerleyen Puberte Olgularında Nihai Boyu Öngörmede Kullanılan Farklı Tahmini Erişkin Boy Hesaplama Yöntemlerinin Etkinliğinin Karşılaştırılması

Akın Kağızmanlı G., Besci Ö., Yüksek Acinikli K., Külekci A. H., Böber E., Demir K., et al.

26. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Türkiye, 26 - 30 Ekim 2022, ss.44

Salivary Sex Steroid Levels in Infants During Minipuberty and Their Relationship with Infantile Colic

METE KALAYCI F., GÜRSOY DORUK Ö., ERBAŞ İ. M., İNCE O. T., TAN M. N., AYDIN A., et al.

60th Annual ESPE (ESPE 2022), ROMA, İtalya, 15 - 17 Eylül 2022, ss.256-257

60th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE)

METE F., GÜRSOY DORUK Ö., ERBAŞ İ. M., İNCE O. T., TAN M. N., AYDIN A., et al.

60th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE)., Roma, İtalya, 15 Eylül 2022, cilt.95, ss.256-257

Tuz kaybettiren konjenital adrenal hiperplazi izleminde 4-saatlik 17- hidroksiprogesteron profilini kullanalım mı?

BESCİ Ö., ERBAŞ İ. M., KÜME T., YÜKSEK ACİNİKLİ K., ABACI A., BÖBER E., et al.

XXV. ULUSAL PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, Antalya, Türkiye, 6 - 10 Kasım 2021, cilt.1, ss.1-5

Serum Sex Hormone Binding Globulin Levels, but not 4-Hour Profile of 17-OH Progesterone, Would be Useful in Monitoring Children with Congenital Adrenal Hyperplasia

BESCİ Ö., ERBAŞ İ. M., KÜME T., YÜKSEK ACİNİKLİ K., ABACI A., BÖBER E., et al.

ESPE 2021 Online, Amerika Birleşik Devletleri, 22 - 26 Eylül 2021, cilt.94, ss.179-180

Circulating C1q Complement/TNF-Related Protein (CTRP)-13 Levels in Obese Children and Its Relationship with Metabolic Disorders

ERBAŞ İ. M., PAKETÇİ A., TURAN S., ŞİŞMAN A., DEMİR K., BÖBER E., et al.

ESPE 2021 Online, İsviçre, 22 Eylül 2021

Büyüme Hormonu Tedavisi Alan Hastalarda Tahmini Erişkin Boy Hesaplama Yöntemlerinin Etkinliğinin Karşılaştırılması

ERBAŞ İ. M., ÖLMEZ Z., PAKETÇİ A., DEMİR K., BÖBER E., ABACI A.

XXIV. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Türkiye, 30 Ekim - 01 Kasım 2020

A Rare Cause of Hypogonadotropic Hypogonadism: FGFR1Mutation

erbas i. m., PAKETÇİ A., acar s., KOTAN GEDİK L. D., DEMİR K., ABACI A., et al.

European Society for Paediatric Endocrinology, 19 - 21 Eylül 2019

Elevated anti-tissue transglutaminase antibodies in children newly diagnosed with type 1 diabetes do not always indicate celiac disease

PAKETÇİ A., ARMAĞAN C., ERBAŞ İ. M., DEMİR K., ABACI A., BÖBER E.

58th Annual Meeting of the European Society for Paediatric Endocrinology, Avusturya, 19 - 21 Eylül 2019, cilt.91, ss.141

PATOLOJİK BOY KISALIĞI OLAN ÇOCUKLARIN HİPOFİZ MANYETİK REZONANS GÖRÜNTÜLEME İNCELEMELERİNDEN YAPILAN ADENOHİPOFİZ UZUNLUK ve HACİM ÖLÇÜMLERİNİN NORMAL BÜYÜME ve GELİŞİME SAHİP ÇOCUKLARIN ÖLÇÜMLERİYLE KARŞILAŞTIRILMASI

Arslan A., SARIOĞLU F. C., DEMİR K., AYSİN M., GÜLERYÜZ H.

24. Türk Manyetik Rezonans Derneği Uluslararası KAtılımlı Bilimsel Toplantısı, 25 - 27 Nisan 2019

Kombine Hipofizer Yetmezlik Tanili 2 Olgu Ve Lhx4 Geni Ekspresyon Değişkenliği

AYYILDIZ EMECEN D., DARCAN Ş., IŞIK E., ABACI A., DEMİR K., BÖBER E., et al.

3. Ege Endokrin Hastalıklar ve Genetik Sempozyumu, Türkiye, 7 - 09 Mart 2019

KOMBİNE HİPOFİZER YETMEZLİK TANILI 2 OLGU VE LHX4 GENİ EKSPRESYON DEĞİŞKENLİĞİ

AYYILDIZ EMECEN D., GÖKŞEN ŞİMŞEK R. D., IŞIK E., ABACI A., DEMİR K., BÖBER E., et al.

3. Ege Endokrin Hastalıklar ve Genetik Sempozyumu, Türkiye, 7 - 09 Mart 2019

Serum Level of Biotin Rather Than the Daily Dose Is the Main Determinant of the Interference on Thyroid Function Assays in Patients with Biotinidase Deficiency

PAKETÇİ A., KÖSE E., GÜRSOY ÇALAN Ö., ACAR S., TEKE KISA P., DEMİRCİ F., et al.

57th Annual Meeting of the European Society for Paediatric Endocrinology in Athens, Greece, 27 - 29 Eylül 2018

Growth Hormone Deficiency Due to Whole-gene Deletion of GHRHR

ACAR S., DEMİR K., KIRBIYIK Ö., PAKETÇİ A., ERDOĞAN K. M., ABACI A., et al.

57th Annual Meeting of the European Society for Paediatric Endocrinology in Athens, Greece, 27 - 29 Eylül 2018

Galanin is Positively Correlated with Insulin Resistance and Triglyceride Levels in Obese Children

ACAR S., PAKETÇİ A., KÜME T., DEMİR K., GÜRSOY ÇALAN Ö., BÖBER E., et al.

57th Annual Meeting of the European Society for Paediatric Endocrinology in Athens, Greece, 27 - 29 Eylül 2018

Nationwide Hypophosphatemic Rickets Study

ŞIKLAR Z., turan s., BEREKET A., ABACI A., BAŞ F., DEMİR K., et al.

57th Annual meeting of ESPE, Atina, Yunanistan, 27 - 29 Eylül 2018, cilt.90, ss.1-680

Çok Merkezli Olarak Hipofosfatemik Riketsli Olguların Değerlendirilmesi

ŞIKLAR Z., TURAN S., BEREKET A., ABACI A., GÜRAN T., DEMİR K., et al.

22. PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, Antalya, Türkiye, 18 - 22 Nisan 2018

Biyotin Tedavisiyle İlişkili sT3 ve sT4 Yüksekliğine Neden Olan Faktörler ve Bu İnterferansı Aşma Yöntemleri

PAKETÇİ A., KÖSE E., GÜRSOY DORUK Ö., ACAR S., TEKE KISA P., DEMİRCİ F., et al.

XXII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Antalya, Türkiye, 18 - 22 Nisan 2018, ss.63

MEDITERRANEAN KIDNEY SOCIETY

DEMİR K., ABACI A., BÖBER E.

MEDITERRANEAN KIDNEY SOCIETY, 1 - 05 Eylül 2017

THE RELATION OF SERUM GALECTIN-1 LEVEL WITH CLINICAL AND METABOLIC PARAMETERS IN OBESE CHILDREN

ACAR S., PAKETÇİ A., KÜME T., ÜNVER TUHAN H., GÜRSOY ÇALAN Ö., DEMİR K., et al.

10th International Meeting of Pediatric Endocrinology:, Washington, Kiribati, 14 - 17 Eylül 2017, cilt.88, ss.1-628

CLINICAL CHARACTERISTICS OF TURKISH CHILDREN AND ADOLESCENTS WITH TYPE 2 DIABETES

HATUN Ş., YEŞİLTEPE MUTLU G., CİNAS P., YILDIZ ERBAŞ M., AKÇAY T., ÖNAL H., et al.

10th International Meeting of Pediatric Endocrinology, Washington, Kiribati, 14 - 17 Eylül 2017 Sürdürülebilir Kalkınma

prop-1 releated combined pituitary hormone deficiency

PAKETÇİ A., ACAR S., DEMİR K., ABACI A., BÖBER E.

2. Ege Endokrin Hastalıklar ve Genetik Sempozyumu, 23 Şubat - 25 Mart 2017, cilt.9, ss.12-13

The Effect of Growth Hormone Therapy on Plasma Phenylalanine Level in Patient with Phenylketonuria: Case Report

KÖSE E., ACAR S., DEMİR K., BERDELİ A., ARSLAN N.

13th International Congress of Inborn Errors Of Metabolism, 5 - 09 Eylül 2017

Clinical and Genetic Features of Our Patients with Hypophosphatemic Rickets

ACAR S., Al Rijal R. A., Meyer B., Shi Y., DEMİR K., BÖBER E., et al.

2. Ege Endocrinology and Genetic Symposium, 23 - 25 Şubat 2017

A Novel Mutation in INSR Gene in a Child Presentingwith Acanthosis Nigricans

ÜNVER TUHAN H., CEYLANER S., NALBANTOĞLU Ö., ACAR S., ABACI A., BÖBER E., et al.

2nd Ege Endocrinology and Genetics Symposium, 23 - 25 Şubat 2017

PROP1-Related Combined Pituitary Hormone Deficiency: Case Report

PAKETÇİ A., ACAR S., DEMİR K., ABACI A., BÖBER E.

2nd Endocrine Diseases and Genetics Symposium, İzmir, Türkiye, 13 - 25 Şubat 2017, cilt.9, ss.1-31

A Novel De Novo Missense Mutation in HNF4AResulting in Sulfonylurea-Responsive MODY

ACAR S., ABACI A., DEMİR K., ÖZDEMİR T. R., ÖZYILMAZ B., BÖBER E.

2nd Endocrine Diseases and Genetics Symposium, İzmir, Türkiye, 23 Şubat 2017, cilt.9, ss.1-31

Büyüme Hormonu Tedavisinin Plazma Fenilalanini Üzerine Etkisi: Olgu Sunumu

KÖSE E., ACAR S., DEMİR K., BERDELİ A., ARSLAN N.

14. Uluslararası Katılımlı Ulusal Metabolik Hastalıklar ve Beslenme Kongresi, 26 - 30 Nisan 2017

Sülfonilüre Yanıtlı MODY’ye Yol Açan, Daha Önce Tanımlanmamış, De Novo, Yanlış Anlamlı (Missense) HNF4A Mutasyonu

ACAR S., ABACI A., DEMİR K., ÖZDEMİR T. R., ÖZYILMAZ B., BÖBER E.

2.Ege Endokrin Hastalıklar ve Genetik Sempozyumu, İzmir, Türkiye, 23 - 25 Şubat 2017

Genetik Tiroid Hormon Direncinin Klinik Özellikleri

DEMİR K.

20. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Türkiye, 6 - 08 Ekim 2016

Kronik malnütrisyonda serum nesfatin-1 düzeyinin, metabolik ve antropometrik parametreler ile olan ilişkisinin değerlendirilmesi

ACAR S., ÇATLI G., KÜME T., ÜNVER TUHAN H., GÜRSOY ÇALAN Ö., DEMİR K., et al.

XX.Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi. Antalya, Türkiye, 5 - 09 Ekim 2016

Spectrum of the Genetic Defects in Hypophosphatemic Rickets in A Group of Turkish Children

ACAR S., Al Rijjal R. A., DEMİR K., Kattan W. E., ÇATLI G., BinEssa H., et al.

55rd Annual Meeting of the European Society for Paediatric Endocrinology (ESPE)., 10 - 12 Eylül 2016

Identi cation of an AR Mutation in Klinefelter s Syndrome during Evaluation for Penoscrotal Hypospadias

ACAR S., ÜNVER TUHAN H., BORA E., DEMİR K., ERÇAL M. D., BÖBER E., et al.

55rd Annual Meeting of the European Society for Paediatric Endocrinology (ESPE)., 10 - 12 Eylül 2016

Retrospective Evaluation of the Efficiency ofMetformin Therapy in Obese Children with InsulinResistance

Çiçek G., ABACI A., ÜNVER TUHAN H., DEMİR K., BÖBER E.

55th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), 10 - 12 Eylül 2016

Retrospective Evaluation of the Ef ciency of MetforminTherapyinObese Childrenwith Insulin Resistance

ÇİÇEK G., ABACI A., ÜNVER TUHAN H., DEMİR K., BÖBER E.

55rd Annual Meeting of the European Society for Paediatric Endocrinology (ESPE)., 10 - 12 Eylül 2016

Identi cation of an AR Mutation in Klinefelter sSyndrome during Evaluation for PenoscrotalHypospadia

ACAR S., ÜNVER TUHAN H., BORA E., DEMİR K., ONAY H., ERÇAL M. D., et al.

55th Annual Meeting of the ESPE, Paris, Fransa, 10 - 12 Eylül 2016, cilt.86, ss.279

Distribution of Mutations in Genes Known to be Associated with Familial Idiopathic Hypogonadotropic Hypogonadism in a Large Cohort

KOTAN L., MENGEN E., GÜRBÜZ F., ÖZSÜ E., TUNÇ E., KOR Y., et al.

54th Annual Meeting of the European Society forPaediatric Endocrinology (ESPE), İspanya, 1 - 03 Ekim 2015, cilt.84, ss.1-622

Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor a Mutations

DEMİR K., van gucht a., büyükinan m., ÇATLI G., AYHAN Y., baş v. n., et al.

54th Annual Meeting of the European Society for Paediatric Endocrinology, 1 - 03 Ekim 2015, ss.122-123

Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malign Infantile Osteopetrosis

DEMİR K., nalbantoğlu ö., karaer k., korkmaz h. a., yıldız m., tunç s., et al.

54th Annual Meeting of the European Society for Paediatric Endocrinology, Barselona, İspanya, 01 Ekim 2015 - 03 Ocak 2016, ss.72-73

EFFECTIVENES OF MAGNETIC RESONANCE IMAGING FOR MEASURING OF PITUITARY IRON OVERLOAD IN PATIENTS WITH THALASSEMIA

Oymak Y., Okur S., Karapinar T. H., Ay Y., DEMİR K., Gurcinar M., et al.

20th Congress of European-Hematology-Association, Vienna, Avusturya, 11 - 14 Haziran 2015, cilt.100, ss.600

ENDOCRINE SIDE EFFECTS AFTER CHEMOTHERAPY IN PATIENTS WITH ACUTE LYMPHOBLASTIC LEUKEMIA

Uysal B., Oymak Y., DEMİR K., Karapinar T. H., Ay Y., Gozmen S., et al.

19th Congress of the European-Hematology-Association, Milan, İtalya, 12 - 15 Haziran 2014, cilt.99, ss.281-282

Vitamin D bağımlı rikets tip 1 İki olgu sunumu

ULUSOY E., DEMİR K., ALTINCIK S. A., ÇATLI G., ABACI A., BEKEM SOYLU Ö., et al.

15. Ulusal Pediatrik Endokrin ve Diyabet Kongresi, Türkiye, 23 - 26 Kasım 2011

Tip 1 diyabetli çocuk ve adolesanlarda böbrek hasarının erken bulgularının araştırılması Notrofil jelatinaz ilişkili lipokalin bir belirteç olabilirmi

DEMİR K., ABACI A., KÜME T., Altıncık A., ÇATLI G., BÖBER E.

15. Ulusal Pediatrik Endokrin ve Diyabet Kongresi, İzmir, Türkiye, 23 - 26 Kasım 2011 Sürdürülebilir Kalkınma

Santral diabetes insipiduslu çocukların klinik,laboratuvar ve etiyolojik özellikleri

ÇATLI G., ABACI A., DEMİR K., ULUSOY E., ALTINCIK S. A., Büyükgebiz A., et al.

15. Ulusal Pediatrik Endokrin ve Diyabet Kongresi, Türkiye, 23 - 26 Kasım 2011 Sürdürülebilir Kalkınma

Can Neutrophil Gelatinase Associated Lipocalin be An Early Marker of Kidney Injury in Type 1 Diabetics

DEMİR K., ABACI A., KÜME T., Altıncık A., ÇATLI G., BÖBER E.

50th Annual Meeting of European Society for Paediatric Endocrinology, Glasgow, UK, 25 - 28 Eylül 2011 Sürdürülebilir Kalkınma

Locus heterogeneity and novel TSHR mutations in consanguineous families with congenital non-goitrous hypothyroidism

Cangul H., SAĞLAM H., Aycan Z., Yakut T., Gulten T., Morgan N. V., et al.

British Human Genetics Conference, Rhode Island, Amerika Birleşik Devletleri, 6 - 08 Eylül 2010, cilt.47

Predictive value of clinical and laboratory parameters for the presence of vesicoureteral reflux in children with urinary tract infection

SOYLU A., Kasap B., DEMİR K., Turkmen M., Kavukcu S.

43rd Annual Congress of the European-Renal-Association/European-Dialysis-and-Transplant-Association (ERA-EDTA), Glasgow, Birleşik Krallık, 15 - 18 Temmuz 2006, cilt.21, ss.93 Sürdürülebilir Kalkınma

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