E-ISSN: 1308-5735 ISSN: 1308-5727

Archives

Volume 9, Issue 1

March 2017

Back to Archives Download Issue

Original Article 9

Review

Non-Classical Congenital Adrenal Hyperplasia in Childhood

Nihal Hatipoglu

Original Article

Subclinical Hypothyroidism in Danish Lean and Obese Children and Adolescents

Johanne Dam Ohrt

Cilius Esmann Fonvig

Julie Tonsgaard Kloppenborg

Jens-Christian Holm

Neck Circumference to Assess Obesity in Preschool Children

Serpil Poyrazoglu

Mümtaz M. Mazicioglu

Role of Versican and ADAMTS-1 in Polycystic Ovary Syndrome

Meryem Kuru Pekcan

Basak Gümüs Güler

Halil Ibrahim Yakut

The Relationship between Serum Zonulin Level and Clinical and Laboratory Parameters of Childhood Obesity

Gönül Çatlı

Özlem Gürsoy Çalan

Comparison of Updated Weight and Height Percentiles with Previous References in 6-17-Year-Old Children in Kayseri, Turkey

Gökmen Zararsiz

M. Mümtaz Mazicioglu

Association Between Endocrine Diseases and Serous Otitis Media in Children

Murat Koçyigit

Taliye Çakabay

Safiye G. Örtekin

Selin Üstün Bezgin

Mustafa Kemal Adali

Clinical and Mutational Features of Three Chinese Children with Congenital Generalized Lipodystrophy

Age-Specific Frequencies and Characteristics of Ovarian Cysts in Children and Adolescents

Hamdi Cihan Emeksiz

Esra Betül Akkoyun

Faruk Güçlü Pinarli

Safety and Efficacy of Stosstherapy in Nutritional Rickets

Daipayan Chatterjee

Mathad K. S. Swamy

Krishti Chatterjee

Case Report

Uniparental Isodisomy of Chromosome 1 Unmasking an Autosomal Recessive 3-Beta Hydroxysteroid Dehydrogenase Type II-Related Congenital Adrenal Hyperplasia

Osayame A. Ekhaguere

Benjamin Darbro

Oleg A. Shchelochkov

Follow-up Findings in a Turkish Girl with Pseudohypoparathyroidism Type Ia Caused by a Novel Heterozygous Mutation in the GNAS Gene

Olcay Evliyaoglu

Beyhan Tüysüz

Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A)

Doga Türkkahraman

Testicular Adrenal Rest Tumor in Two Brothers with a Novel Mutation in the 3-Beta-Hydroxysteroid Dehydrogenase-2 Gene

A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene

Meliksah Keskin

Nursel Muratoglu Sahin

Elvan Bayramoglu

Senay Savas Erdeve

Semra Çetinkaya