Dergiler / Journal of Clinical Research in Pediatric Endocrinology

2016 · Cilt: 8 - Sayı: 4

MakaleYazarSayfa
Current Status of Childhood Hyperinsulinemic Hypoglycemia in TurkeyZEYNEP ŞIKLAR,MERİH BERBEROĞLU375–380
Breast-Milk Iodine Concentrations, Iodine Status, and Thyroid Function of Breastfed Infants Aged 2-4 Months and Their Mothers Residing in a South African TownshipJennifer OSEİ,Maria ANDERSSON2,Olivia van der REİJDEN2,Susanne DOLD2,Cornelius M. SMUTS,Jeannine BAUMGARTNER381–391
Luteinizing Hormone Secretion during Gonadotropin-Releasing Hormone Stimulation Tests in Obese Girls with Central Precocious PubertyHae Sang LEE,Jong Seo YOON,Jin Soon HWANG392–398
The Role of Osteopontin in the Pathogenesis and Complications of Type 1 Diabetes Mellitus in ChildrenMohamed A. TALAT,Laila Metwaly SHERİEF,Hosam Fathy EL-SAADANY,Anwar Ahmed RASS,Rabab M. SALEH,Maha Mahmoud Hamed SAKR399–404
Association between Common Genetic Variants and Polycystic Ovary Syndrome Risk in a Chinese Han PopulationYing SUN,Yi YUAN,Hua YANG,Jingjie Lİ,Tian FENG,Yongri OUYANG,Tianbo JİN,Ming LİU405–410
Development and Validation of a Pediatric Endocrine Knowledge Assessment Questionnaire: Impact of ac Pediatric Endocrine Knowledge Assessment Questionnaire Intervention StudyNidhi GUPTA,Marwan ZİDAN,Kathleen MOLTZ,Amita ADHİKARİ,Colleen SAXTON BUGGS,Hanaa ZİDAN,Dania ABUSHANAB,Aida LTEİF,Chandra EDWİN411–418
The 13C-Glucose Breath Test for Insulin Resistance Assessment in Adolescents: Comparison with Fasting and Post-Glucose Stimulus Surrogate Markers of Insulin ResistanceJorge MALDONADO-HERNÁNDEZ,Azucena MARTÍNEZ-BASİLA,Alejandra SALAS-FERNÁNDEZ,José R. NAVARRO-BETANCOURT,Mónica I. PİÑA-AGUERO,Mariela BERNABE-GARCÍA419–424
Lower Plasma Ghrelin Levels are Found in Women with DiabetesComplicated PregnanciesRita 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. WACHER425–431
Pseudohypoparathyroidism Type 1A-Subclinical Hypothyroidism and Rapid Weight Gain as Early Clinical Signs: A Clinical Review of 10 CasesSimon KAYEMBA-KAY'S,Cedric TRİPON,Anne HERON,Peter HİNDMARSH432–438
The Effect of Congenital and Postnatal Hypothyroidism on Depression-Like Behaviors in Juvenile RatsERDOĞAN ÖZGÜR,Börte Gürbüz ÖZGÜR,HATİCE AKSU,GÖKHAN CESUR439–444
Vitamin D Deficiency in Pediatric Fracture Patients: Prevalence, Risk Factors, and Vitamin D SupplementationErwin A GORTER,Wilma OOSTDİJK,Abraham FELİUS,Pieta KRİJNEN,Inger B SCHİPPER445–451
Effect of Cytokine Signaling 3 Gene Polymorphisms in Childhood ObesityMehmet BOYRAZ,Ediz YEŞİLKAYA,FATİH SÜHEYL EZGÜ,AYSUN BİDECİ,Haldun DOĞAN,Korkut ULUCAN,PEYAMİ CİNAZ452–460
Prevalence of Vitamin D Deficiency and Calcium Homeostasis in Saudi ChildrenAdnan 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 MUKHTAR461–467
Complex Glycerol Kinase Deficiency and Adrenocortical Insufficiency in Two NeonatesSabriye KORKUT,Osman BAŞTUĞ,Margarita RAYGADA,Nihal HATİPOĞLU,Selim KURTOĞLU,MUSTAFA KENDİRCİ,Charalampos LYSSİKATOS,Constantine A. STRATAKİS468–471
A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish FamilyFatma DURSUN,Hussein Sheikh Ali MOHAMOUD,Noreen KARİM,Muhammad NAEEM,Musharraf JELANİ,Heves KIRMIZIBEKMEZ472–477
A Novel Homozygous Mutation in the KCNJ11 Gene of a Neonate with Congenital Hyperinsulinism and Successful Management with SirolimusSevim ÜNAL,Deniz GÖNÜLAL,Ahmet UÇAKTÜRK,Betül BİLGİN SİYAH,Sarah E FLANAGAN,FATİH GÜRBÜZ,Meltem TAYFUN,Selin ELMAOĞULLARI,Aslıhan ARASLI,Fatma DEMİREL,Sian ELLARD,Khalid HUSSAIN478–481
A p.(Glu809Lys) Mutation in the WFS1 Gene Associated with Wolfram-like Syndrome: A Case ReportDagmar PROCHAZKOVA,Zuzana HRUBA,Petra KONECNA,Jarmila SKOTAKOVA,Lenka FAJKUSOVA482–483
A Case of Vitamin D-Dependent Rickets Type 1A with a Novel Mutation in the Uzbek PopulationBahar ÖZCABI,Feride BUCAK TAHMİSCİOĞLU,Sevinç JAFEROVA,Çiğdem ORUÇ,Amra ADROVİÇ,Serdar CEYLANER,OYA ERCAN,SAADET OLCAY EVLİYAOĞLU484–489
A Critical Appraisal of Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome Patients in TurkeyZehra Yavaş ABALI,FATMA FEYZA DARENDELİLER,Olcay Neyzi490–495
Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene MutationFATİH GÜRBÜZ,BİLGİN YÜKSEL,Ali Kemal TOPALOĞLU496–497