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Diabetes Research and Clinical Practice|October 31, 2012
Permanent neonatal diabetes caused by a novel mutation in the INS geneGonul Catli, Ayhan Abaci, Sarah E Flanagan, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 19, 2013
Hyperprolactinemia in children: clinical features and long-term resultsGonul Catli, Ayhan Abaci, Ayca Altincik, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 6, 2015
Levothyroxine replacement in primary congenital hypothyroidism: the higher the initial dose the higher the rate of overtreatmentHale Tuhan, Ayhan Abaci, Gizem Cicek, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 11, 2012
Clinical profile and etiologies of children with central diabetes insipidus: a single-center experience from TurkeyGonul Catli, Ayhan Abaci, Korcan Demir, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 16, 2014
Cross-reactivity of adrenal steroids with aldosterone may prevent the accurate diagnosis of congenital adrenal hyperplasiaHale Unver Tuhan, Gonul Catli, Ahmet Anik, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 28, 2014
A novel missense mutation in HSD17B3 gene in a 46, XY adolescent presenting with primary amenorrhea and virilization at pubertyHale Unver Tuhan, Ahmet Anik, Gonul Catli, et al.
Journal of Diabetes and Its Complications|April 17, 2008
Hepatic glycogenosis: a rare cause of hepatomegaly in Type 1 diabetes mellitusAyhan Abaci, Ozlem Bekem, Tolga Unuvar, et al.
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