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Calcified Tissue International|February 24, 2020
Clinical Significance of Hypophosphatasemia in ChildrenRana Bayramli, Tulay Cevlik, Tulay Guran, et al.Clinical Endocrinology|June 4, 2016
GCK gene mutations are a common cause of childhood-onset MODY (maturity-onset diabetes of the young) in TurkeyBelma Haliloglu, Gerald Hysenaj, Zeynep Atay, et al.Hormone Research in Paediatrics|December 3, 2025
The Mystery of Elevated β-hCG in GnRH-Independent Precocious Puberty without a Detectable Tumor: A Six-Year Diagnostic OdysseyDidem Helvacioglu, Azad Akberzade, Saygin Abali, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 15, 2011
Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia: novel mutations in TRPM6 and CLDN16 genesTulay Guran, Teoman Akcay, Abdullah Bereket, et al.Gene|December 14, 2012
A novel homozygous TMEM70 mutation results in congenital cataract and neonatal mitochondrial encephalo-cardiomyopathyZeynep Atay, Abdullah Bereket, Serap Turan, et al.Pituitary|August 23, 2014
Effects of leukemia inhibitory receptor gene mutations on human hypothalamo-pituitary-adrenal functionTulay Guran, Omer Guran, Cem Paketci, et al.Bone|December 3, 2014
Evidence of hormone resistance in a pseudo-pseudohypoparathyroidism patient with a novel paternal mutation in GNASSerap Turan, Susanne Thiele, Olta Tafaj, et al.Journal of Clinical Research in Pediatric Endocrinology|November 28, 2017
The Distribution of Different Types of Diabetes in Childhood: A Single Center ExperienceBelma Haliloğlu, Saygın Abalı, Fuat Buğrul, et al.The Journal of Clinical Endocrinology and Metabolism|February 17, 2012
An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R (T152K) and MC1R (R160W)Serap Turan, Claire Hughes, Zeynep Atay, et al.Pediatric Diabetes|November 23, 2016
Hypoglycemia is common in children with cystic fibrosis and seen predominantly in femalesBelma Haliloglu, Yasemin Gokdemir, Zeynep Atay, et al.Pageof 6