Editorial
Neonatal Hypopituitarism: Approaches to Diagnosis and Treatment
Selim Kurtoğlu, Ahmet Özdemir, Nihal Hatipoğlu
Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants
Tülay Güran, Başak Tezel, Fatih Gürbüz, et al.
Androgen Insensitivity Syndrome: Clinical Phenotype and Molecular Analysis in a Single Tertiary Center Cohort
Maria Sol Touzon, Natalia Perez Garrido, Roxana Marino, et al.
Genetic and Clinical Characteristics of Patients with Vitamin D Dependent Rickets Type 1A
Fatma Dursun, Gamze Özgürhan, Heves Kırmızıbekmez, et al.
Birth Size in Neonates with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency
Helmuth G. Dörr, Theresa Penger, Andrea Albrecht, et al.
Evaluation of Renal Function in Obese Children and Adolescents Using Serum Cystatin C Levels, Estimated Glomerular Filtration Rate Formulae and Proteinuria: Which is most Useful?
Dilşah Önerli Salman, Zeynep Şıklar, Eda Nisa Çullas İlarslan, et al.
SLC30A8 Gene rs13266634 C/T Polymorphism in Children with Type 1 Diabetes in Tamil Nadu, India
Ramasamy Thirunavukkarasu, Arthur Joseph Asirvatham, Ayyappan Chitra, et al.
Epicardial Fat Thickness in Children with Classic Congenital Adrenal Hyperplasia
Kotb Abbass Metwalley, Hekma Saad Farghaly, Abdelrahman Abdelhamid
Effect of Telehealth System on Glycemic Control in Children and Adolescents with Type 1 Diabetes
Esra Döğer, Rukiye Bozbulut, A. Şebnem Soysal Acar, et al.
Remarkable Increase in the Prevalence of Overweight and Obesity Among School Age Children in Antalya, Turkey, Between 2003 and 2015
Gamze Çelmeli, Yusuf Çürek, Zümrüt Arslan Gülten, et al.
Congenital Hyperinsulinism and Evolution to Sulfonylurearesponsive Diabetes Later in Life due to a Novel Homozygous p.L171F ABCC8 Mutation
Emregül Işık, Hüseyin Demirbilek, Jayne A. Houghton, et al.
Inherited Deletion of 1q, Hyperparathyroidism and Signs of Y-chromosomal Influence in a Patient with Turner Syndrome
Alejandro F. Siller, Alex Shimony, Marwan Shinawi, et al.
Hyperphosphatemic Familial Tumoral Calcinosis in Two Siblings with a Novel Mutation in GALNT3 Gene: Experience from Southern Turkey
Rabia Miray Kışla Ekinci, Fatih Gürbüz, Sibel Balcı, et al.
Severe Neonatal Cholestasis as an Early Presentation of McCune- Albright Syndrome
Nicole Coles, Ian Comeau, Tatiana Munoz, et al.
Extreme Premature Small for Gestational Age Infants Have Appropriate Catch-up Growth at Term Equivalence Compared with Extreme Premature Appropriate for Gestational Age Infants
Sze May Ng, Donatella Pintus, Mark A. Turner
