Review
Non-Classical Congenital Adrenal Hyperplasia in Childhood
Selim Kurtoglu, Nihal Hatipoglu
Subclinical Hypothyroidism in Danish Lean and Obese Children and Adolescents
Maria Dahl, Johanne Dam Ohrt, Cilius Esmann Fonvig, et al.
Neck Circumference to Assess Obesity in Preschool Children
Meda Kondolot, Duygu Horoz, Serpil Poyrazoglu, et al.
Role of Versican and ADAMTS-1 in Polycystic Ovary Syndrome
Sibel Özler, Efser Öztaş, Aytekin Tokmak, et al.
The Relationship between Serum Zonulin Level and Clinical and Laboratory Parameters of Childhood Obesity
Tuncay Küme, Sezer Acar, Hale Tuhan, et al.
Comparison of Updated Weight and Height Percentiles with Previous References in 6-17-Year-Old Children in Kayseri, Turkey
Gökmen Zararsiz, Betül Çiçek, Meda Kondolot, et al.
Association Between Endocrine Diseases and Serous Otitis Media in Children
Murat Koçyigit, Taliye Çakabay, Safiye G. Örtekin, et al.
Clinical and Mutational Features of Three Chinese Children with Congenital Generalized Lipodystrophy
Xueying Su, Ruizhu Lin, Yonglan Huang, et al.
Age-Specific Frequencies and Characteristics of Ovarian Cysts in Children and Adolescents
Hamdi Cihan Emeksiz, Oksan Derinöz, Esra Betül Akkoyun, et al.
Safety and Efficacy of Stosstherapy in Nutritional Rickets
Daipayan Chatterjee, Mathad K. S. Swamy, Vikas Gupta, et al.
Uniparental Isodisomy of Chromosome 1 Unmasking an Autosomal Recessive 3-Beta Hydroxysteroid Dehydrogenase Type II-Related Congenital Adrenal Hyperplasia
Karin Panzer, Osayame A. Ekhaguere, Benjamin Darbro, et al.
Follow-up Findings in a Turkish Girl with Pseudohypoparathyroidism Type Ia Caused by a Novel Heterozygous Mutation in the GNAS Gene
Sezgin Sahin, Olaf Hiort, Susanne Thiele, et al.
Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A)
Gamze Çelmeli, Doga Türkkahraman, Yusuf Çürek, et al.
A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene
Meliksah Keskin, Nursel Muratoglu Sahin, Erdal Kurnaz, et al.
