Luteinizing Hormone Secretion during Gonadotropin-Releasing Hormone Stimulation Tests in Obese Girls with Central Precocious Puberty

Hae Sang LEE, Jong Seo YOON, Jin Soon HWANG

The Effect of Congenital and Postnatal Hypothyroidism on Depression-Like Behaviors in Juvenile Rats

ERDOĞAN ÖZGÜR, Börte Gürbüz ÖZGÜR, HATİCE AKSU, GÖKHAN CESUR

Prevalence of Vitamin D Deficiency and Calcium Homeostasis in Saudi Children

Adnan M Al SHAİKH, Bahaa ABAALKHAİL, Ashraf SOLIMAN, Ibrahim KADDAM, Khalid ASERİ, Yousef Al SALEH, Ali Al QARNİ, Ahmed Al SHUAİBİ, Waleed Al TAMİMİ, Abdel Moniem MUKHTAR

Complex Glycerol Kinase Deficiency and Adrenocortical Insufficiency in Two Neonates

Sabriye KORKUT, Osman BAŞTUĞ, Margarita RAYGADA, Nihal HATİPOĞLU, Selim KURTOĞLU, MUSTAFA KENDİRCİ, Charalampos LYSSİKATOS, Constantine A. STRATAKİS

A p.(Glu809Lys) Mutation in the WFS1 Gene Associated with Wolfram-like Syndrome: A Case Report

Dagmar PROCHAZKOVA, Zuzana HRUBA, Petra KONECNA, Jarmila SKOTAKOVA, Lenka FAJKUSOVA

A Case of Vitamin D-Dependent Rickets Type 1A with a Novel Mutation in the Uzbek Population

Bahar ÖZCABI, Feride BUCAK TAHMİSCİOĞLU, Sevinç JAFEROVA, Çiğdem ORUÇ, Amra ADROVİÇ, Serdar CEYLANER, OYA ERCAN, SAADET OLCAY EVLİYAOĞLU

Current Status of Childhood Hyperinsulinemic Hypoglycemia in Turkey

ZEYNEP ŞIKLAR, MERİH BERBEROĞLU

The 13C-Glucose Breath Test for Insulin Resistance Assessment in Adolescents: Comparison with Fasting and Post-Glucose Stimulus Surrogate Markers of Insulin Resistance

Jorge MALDONADO-HERNÁNDEZ, Azucena MARTÍNEZ-BASİLA, Alejandra SALAS-FERNÁNDEZ, José R. NAVARRO-BETANCOURT, Mónica I. PİÑA-AGUERO, Mariela BERNABE-GARCÍA

Vitamin D Deficiency in Pediatric Fracture Patients: Prevalence, Risk Factors, and Vitamin D Supplementation

Erwin A GORTER, Wilma OOSTDİJK, Abraham FELİUS, Pieta KRİJNEN, Inger B SCHİPPER

Effect of Cytokine Signaling 3 Gene Polymorphisms in Childhood Obesity

Mehmet BOYRAZ, Ediz YEŞİLKAYA, FATİH SÜHEYL EZGÜ, AYSUN BİDECİ, Haldun DOĞAN, Korkut ULUCAN, PEYAMİ CİNAZ

Breast-Milk Iodine Concentrations, Iodine Status, and Thyroid Function of Breastfed Infants Aged 2-4 Months and Their Mothers Residing in a South African Township

Jennifer OSEİ, Maria ANDERSSON2, Olivia van der REİJDEN2, Susanne DOLD2, Cornelius M. SMUTS, Jeannine BAUMGARTNER

The Role of Osteopontin in the Pathogenesis and Complications of Type 1 Diabetes Mellitus in Children

Mohamed A. TALAT, Laila Metwaly SHERİEF, Hosam Fathy EL-SAADANY, Anwar Ahmed RASS, Rabab M. SALEH, Maha Mahmoud Hamed SAKR

Association between Common Genetic Variants and Polycystic Ovary Syndrome Risk in a Chinese Han Population

Ying SUN, Yi YUAN, Hua YANG, Jingjie Lİ, Tian FENG, Yongri OUYANG, Tianbo JİN, Ming LİU

Development and Validation of a Pediatric Endocrine Knowledge Assessment Questionnaire: Impact of ac Pediatric Endocrine Knowledge Assessment Questionnaire Intervention Study

Nidhi GUPTA, Marwan ZİDAN, Kathleen MOLTZ, Amita ADHİKARİ, Colleen SAXTON BUGGS, Hanaa ZİDAN, Dania ABUSHANAB, Aida LTEİF, Chandra EDWİN

Lower Plasma Ghrelin Levels are Found in Women with DiabetesComplicated Pregnancies

Rita Angélica GÓMEZ-DÍAZ, Monica P. GÓMEZ-MEDİNA, Eleazar RAMÍREZ-SORİANO, Lucio LÓPEZ-ROBLES, Carlos A. AGUİLAR-SALİNAS, Renata SAUCEDO, Arturo ZARATE, Adan VALLADARES-SALGADO, Niels H. WACHER

Pseudohypoparathyroidism Type 1A-Subclinical Hypothyroidism and Rapid Weight Gain as Early Clinical Signs: A Clinical Review of 10 Cases

Simon KAYEMBA-KAY'S, Cedric TRİPON, Anne HERON, Peter HİNDMARSH

A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family

Fatma DURSUN, Hussein Sheikh Ali MOHAMOUD, Noreen KARİM, Muhammad NAEEM, Musharraf JELANİ, Heves KIRMIZIBEKMEZ

A Novel Homozygous Mutation in the KCNJ11 Gene of a Neonate with Congenital Hyperinsulinism and Successful Management with Sirolimus

Sevim ÜNAL, Deniz GÖNÜLAL, Ahmet UÇAKTÜRK, Betül BİLGİN SİYAH, Sarah E FLANAGAN, FATİH GÜRBÜZ, Meltem TAYFUN, Selin ELMAOĞULLARI, Aslıhan ARASLI, Fatma DEMİREL, Sian ELLARD, Khalid HUSSAIN

A Critical Appraisal of Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome Patients in Turkey

Zehra Yavaş ABALI, FATMA FEYZA DARENDELİLER, Olcay Neyzi

Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation

FATİH GÜRBÜZ, BİLGİN YÜKSEL, Ali Kemal TOPALOĞLU