Teoman Akçay

Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile Hypercalcemia

Karl P. Schlingmann, Justyna Ruminska, Martin Kaufmann et al. · Journal of the American Society of Nephrology · 2015 · 282 citations · Full text

Medicine, Endocrinology, Genetics +17

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

Tülay Güran, Federica Buonocore, Nurçin Saka et al. · The Journal of Clinical Endocrinology & Metabolism · 2015 · 212 citations · Full text

Medicine, Endocrinology, Pediatrics +16

Serum Alkaline Phosphatase Levels in Healthy Children and Evaluation of Alkaline Phosphatase z-scores in Different Types of Rickets

Serap Turan, Burcu Topçu, İbrahim Gökçe et al. · Journal of Clinical Research in Pediatric Endocrinology · 2011 · 159 citations · Full text

Medicine, Child Health, Pediatrics +10

Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF4A gene mutations

Sarah E. Flanagan, Ritika R. Kapoor, G Mali et al. · European Journal of Endocrinology · 2010 · 143 citations · Full text

Medicine, Genetics, Molecular Genetics +11

Hypogonadotropic Hypogonadism due to a Novel Missense Mutation in the First Extracellular Loop of the Neurokinin B Receptor

Tülay Güran, Gwen Tolhurst, Abdullah Bereket et al. · The Journal of Clinical Endocrinology & Metabolism · 2009 · 135 citations · Full text

Medicine, Endocrinology, Genetics +15