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Magnesium Research|April 15, 2011
Cognitive and psychosocial development in children with familial hypomagnesaemiaTulay Guran, Ayse Arman, Teoman Akcay, et al.European Journal of Pediatrics|October 25, 2012
Infantile loss of teeth: odontohypophosphatasia or childhood hypophosphatasiaBelma Haliloglu, Tulay Guran, Zeynep Atay, et al.Hormone Research in Paediatrics|February 14, 2015
Premature pubarche, hyperinsulinemia and hypothyroxinemia: novel manifestations of congenital portosystemic shunts (Abernethy malformation) in childrenSerpil Bas, Tulay Guran, Zeynep Atay, et al.Pediatric Radiology|May 8, 2024
Evaluating breast ultrasonography as a complementary diagnostic method in girls with central precocious pubertyErhan Bıyıklı, Didem Helvacıoğlu, Onur Buğdaycı, et al.The Journal of Clinical Endocrinology and Metabolism|June 26, 2026
Machine Learning Algorithms to Accelerate Etiological Diagnosis of Congenital Disorders of Adrenal SteroidogenesisBusra Gurpinar Tosun, Atam Noyan Erçetin, Serap Turan, et al.The Turkish Journal of Pediatrics|December 26, 2017
Persistent hyperglycemia in a neonate: Is it a complication of therapeutic hypothermia?Hülya Özdemir, Aslı Memişoğlu, Zeynep Alp-Unkar, et al.Journal of Endocrinological Investigation|June 24, 2026
Determinants of pubertal progression and final height in premature pubarcheDidem Helvacioglu, Aylin Tugba Canbaz, Mehmet Eltan, et al.Clinical Genetics|February 27, 2023
Two new cases with novel pathogenic variants reflecting the clinical diversity of Schaaf-Yang syndromeCeren Alavanda, Esra Arslan Ateş, Zehra Yavaş Abalı, et al.International Journal of Endocrinology|June 6, 2013
Maternal thyroid dysfunction and neonatal thyroid problemsHulya Ozdemir, Ipek Akman, Senay Coskun, et al.Hormone Research|October 28, 2008
Screening of parents and siblings of patients with thyroid dysgenesis by thyroid function tests and ultrasoundElif Karakoc, Serap Turan, Ihsan Akpinar, et al.Pageof 16