Subclinical Hypothyroidism in Danish Lean and Obese Children and Adolescents

Maria DAHL, Johanne Dam OHRT, Cilius Esmann FONVİG, Julie Tonsgaard KLOPPENBORG, Oluf PEDERSEN, Torben HANSEN, Jens-Christian HOLM

Role of Versican and ADAMTS-1 in Polycystic Ovary Syndrome

SİBEL ÖZLER, Efser ÖZTAŞ, Aytekin TOKMAK, Merve ERGİN, Meryem Kuru PEKCAN, Başak GÜMÜŞ GÜLER, HALİL İBRAHİM YAKUT, NAFİYE YILMAZ

Non-Classical Congenital Adrenal Hyperplasia in Childhood

Selim KURTOĞLU, Nihal HATİPOĞLU

Neck Circumference to Assess Obesity in Preschool Children

MEDA KONDOLOT, Duygu HOROZ, Serpil POYRAZOĞLU, ARDA BORLU, AHMET ÖZTÜRK, Selim KURTOĞLU, Mümtaz M. MAZICIOĞLU

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

TUNCAY KÜME, Sezer ACAR, HALE ÜNVER TUHAN, GÖNÜL ÇATLI, AHMET ANIK, Özlem GÜRSOY ÇALAN, ECE BÖBER, AYHAN ABACI

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

Gamze ÇELMELİ, DOĞA TÜRKKAHRAMAN, Yusuf ÇÜREK, Jayne HOUGHTON, Sema AKÇURİN, İffet BİRCAN

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

GÖKMEN ZARARSIZ, BETÜL ÇİÇEK, MEDA KONDOLOT, M MÜMTAZ MAZICIOĞLU, AHMET ÖZTÜRK, Selim KURTOĞLU

Association Between Endocrine Diseases and Serous Otitis Media in Children

Murat KOÇYİĞİT, Taliye ÇAKABAY, Safiye G ÖRTEKİN, Teoman AKÇAY, GÜVEN ÖZKAYA, Selin Üstün BEZGİN, Melek YILDIZ, Mustafa Kemal ADALI

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

Xueying SU, Ruizhu LİN, Yonglan HUANG, Huiying SHENG, Xiaofei LI, Tzer Hwu TİNG, Li LIU, Xiuzhen Lİ

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

HAMDİ CİHAN EMEKSİZ, Okşan DERİNÖZ, Esra Betül AKKOYUN, FARUK GÜÇLÜ PINARLI, AYSUN BİDECİ

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

AYLA GÜVEN, Seher POLAT

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, Jennifer COOK, Oleg A SHCHELOCHKOV

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

Melikşah KESKİN, Nursel Muratoğlu ŞAHİN, Erdal KURNAZ, Elvan BAYRAMOĞLU, ŞENAY SAVAŞ ERDEVE, ZEHRA AYCAN, SEMRA ÇETİNKAYA

Safety and Efficacy of Stosstherapy in Nutritional Rickets

Daipayan CHATTERJEE, Vikas GUPTA, Vasu SHARMA, Akshat SHARMA, Krishti CHATTERJEE

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

Sezgin ŞAHİN, Olaf HİORT, Susanne THİELE, SAADET OLCAY EVLİYAOĞLU, BEYHAN TÜYSÜZ