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Journal of Pediatric Endocrinology & Metabolism : JPEM|February 8, 2012
Characteristics and prevalence of non-classical congenital adrenal hyperplasia with a V2811 mutation in patients with premature pubarcheSenay Savas Erdeve, Merih Berberoglu, Nüket Yurur-Kutlay, et al.Indian Journal of Pediatrics|March 13, 2008
Hypophosphatasia associated with pseudotumor cerebri and respiratory insufficiencySerap Teber, Taner Sezer, Mehpare Kafali, et al.Clinical Endocrinology|June 26, 2023
Evaluation of aggression level in adolescent girls with classical congenital adrenal hyperplasiaRecep Oğuzhan Isik, Sirmen Kizilcan Cetin, Semra Cetinkaya, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|March 28, 2006
Isolated central diabetes insipidus in a newborn with congenital toxoplasmosisAhmet Karadag, Omer Erdeve, Begum Atasay, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|March 3, 2006
Incidence of iodine deficiency in patients presenting with goitre--discrepancy between clinical and ultrasonographic evaluation of the thyroid: comparison of patients with and without autoimmune thyroiditis--clinical, hormonal and urinary iodine excretion studiesOlcay Evliyaoglu, Merih Berberoglu, Pelin Adiyaman, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|July 1, 2026
Steroid profiling in congenital adrenal hyperplasia: comparing immunoassays and LC-MS/MS accuracyShahla Taba-Tabai, Elif Ozsu, Sirmen Kizilcan Cetin, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|December 2, 2004
Latent autoimmune diabetes mellitus in children (LADC) with autoimmune thyroiditis and Celiac diseaseZehra Aycan, Merih Berberoglu, Pelin Adiyaman, et al.Klinische Padiatrie|February 3, 2022
Does Metformin Treatment in Pediatric Population Cause Vitamin B12 Deficiency?Özen Taş, Tugba Kontbay, Ozlem Dogan, et al.European Journal of Pediatrics|February 25, 2010
A novel mutation of 5alpha-steroid reductase 2 deficiency (CD 65 ALA-PRO) with severe virilization defect in a Turkish family and difficulty in gender assignmentSenay Savas Erdeve, Zehra Aycan, Merih Berberoglu, et al.Hormone Research in Paediatrics|May 14, 2016
Coexistence of Mosaic Uniparental Isodisomy and a KCNJ11 Mutation Presenting as Diffuse Congenital Hyperinsulinism and HemihypertrophyPınar Kocaay, Zeynep Şiklar, Sian Ellard, et al.Pageof 5