Other
Current Status of Childhood Hyperinsulinemic Hypoglycemia in Turkey
Zeynep Şıklar, Merih Berberoğlu
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 Osei, Maria Andersson, Olivia van der Reijden, et al.
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 Role of Osteopontin in the Pathogenesis and Complications of Type 1 Diabetes Mellitus in Children
Mohamed A. Talat, Laila Metwaly Sherief, Hosam Fathy El-Saadany, et al.
Association between Common Genetic Variants and Polycystic Ovary Syndrome Risk in a Chinese Han Population
Ying Sun, Yi Yuan, Hua Yang, et al.
Development and Validation of a Pediatric Endocrine Knowledge Assessment Questionnaire: Impact of ac Pediatric Endocrine Knowledge Assessment Questionnaire Intervention Study
Nidhi Gupta, Marwan Zidan, Kathleen Moltz, et al.
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-Basila, Alejandra Salas-Fernández, et al.
Lower Plasma Ghrelin Levels are Found in Women with Diabetes-Complicated Pregnancies
Rita Angélica Gómez-Díaz, Monica P. Gómez-Medina, Eleazar Ramírez-Soriano, et al.
Pseudohypoparathyroidism Type 1A-Subclinical Hypothyroidism and Rapid Weight Gain as Early Clinical Signs: A Clinical Review of 10 Cases
Simon Kayemba-Kay’s, Cedric Tripon, Anne Heron, et al.
The Effect of Congenital and Postnatal Hypothyroidism on Depression-Like Behaviors in Juvenile Rats
Erdoğan Özgür, Börte Gürbüz Özgür, Hatice Aksu, et al.
Vitamin D Deficiency in Pediatric Fracture Patients: Prevalence, Risk Factors, and Vitamin D Supplementation
Erwin A. Gorter, Wilma Oostdijk, Abraham Felius, et al.
Effect of Cytokine Signaling 3 Gene Polymorphisms in Childhood Obesity
Mehmet Boyraz, Ediz Yeşilkaya, Fatih Ezgü, et al.
Prevalence of Vitamin D Deficiency and Calcium Homeostasis in Saudi Children
Adnan M. Al Shaikh, Bahaa Abaalkhail, Ashraf Soliman, et al.
Complex Glycerol Kinase Deficiency and Adrenocortical Insufficiency in Two Neonates
Sabriye Korkut, Osman Baştuğ, Margarita Raygada, et al.
A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family
Fatma Dursun, Hussein Sheikh Ali Mohamoud, Noreen Karim, et al.
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, et al.
A p.(Glu809Lys) Mutation in the WFS1 Gene Associated with Wolfram-like Syndrome: A Case Report
Dagmar Prochazkova, Zuzana Hruba, Petra Konecna, et al.
A Case of Vitamin D-Dependent Rickets Type 1A with a Novel Mutation in the Uzbek Population
Bahar Özcabı, Feride Tahmiscioğlu Bucak, Sevinç Jaferova, et al.
A Critical Appraisal of Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome Patients in Turkey
Zehra Yavaş Abalı, Feyza Darendeliler, Olcay Neyzi
Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation
Fatih Gürbüz, Bilgin Yüksel, Ali Kemal Topaloğlu
