| Editorial: Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey | Abdullah BEREKET | 1–3 |
| Neonatal Hypopituitarism: Approaches to Diagnosis and Treatment | Selim KURTOĞLU,AHMET ÖZDEMİR,Nihal HATİPOĞLU | 4–12 |
| Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants | Tülay GÜRAN,Başak TEZEL,FATİH GÜRBÜZ,Beray EKLİOĞLU,Nihal HATİPOĞLU,Cengiz KARA,Enver ŞİMŞEK,Filiz ÇİZMECİOĞLU,Alev OZON,Firdevs BAŞ,Murat AYDIN,Feyza DARENDELİLER | 13–23 |
| Androgen Insensitivity Syndrome: Clinical Phenotype and Molecular Analysis in a Single Tertiary Center Cohort | Maria Sol TOUZON,Natalia Perez GARRİDO,Roxana MARİNO,Pablo RAMİREZ,Mariana COSTANZO,Gabriela GUERCİO,Esperanza BERENSZTEİN,Marco A. RİVAROLA,Alicia BELGOROSKY | 24–33 |
| Genetic and Clinical Characteristics of Patients with Vitamin D Dependent Rickets Type 1A | Fatma DURSUN,Gamze ÖZGÜRHAN,Heves KIRMIZIBEKMEZ,Ece KESKİN,Bülent HACIHAMDİOĞLU | 34–40 |
| Birth Size in Neonates with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency | Helmuth G. DÖRR,Theresa PENGER,Andrea ALBRECHT,Michaela MARX,Thomas M. K. VÖLKL | 41–45 |
| 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 ÖNERLİ SALMAN,ZEYNEP ŞIKLAR,NİSA EDA ÇULLAS İLARSLAN,Z. Birsin ÖZÇALAR,Pınar KOCAAY,MERİH BERBEROĞLU | 46–54 |
| SLC30A8 Gene rs13266634 C/T Polymorphism in Children with Type 1 Diabetes in Tamil Nadu, India | Ramasamy THIRUNAVUKKARASU,Arthur Joseph ASIRVATHAM,Ayyappan CHITRA,Mariakuttikan JAYALAKSHMI | 55–60 |
| Epicardial Fat Thickness in Children with Classic Congenital Adrenal Hyperplasia | Kotb Abbass METWALLEY,Hekma Saad FARGHALY,Abdelrahman ABDELHAMİD | 61–69 |
| Effect of Telehealth System on Glycemic Control in Children and Adolescents with Type 1 Diabetes | ESRA DÖĞER,Rukiye BOZBULUT,A. Şebnem SOYSAL ACAR,Aylin KILINÇ UĞURLU,Emine Demet AKBAŞ,AYSUN BİDECİ,MAHMUT ORHUN ÇAMURDAN,PEYAMİ CİNAZ | 70–75 |
| Remarkable Increase in the Prevalence of Overweight and Obesity Among School Age Children in Antalya, Turkey, Between 2003 and 2015 | Gamze ÇELMELİ,Yusuf ÇÜREK,Zümrüt ARSLAN GÜLTEN,Mehmet YARDIMSEVER,MUSTAFA KOYUN,Sema AKÇURİN,İffet BİRCAN | 76–81 |
| Congenital Hyperinsulinism and Evolution to Sulfonylurearesponsive Diabetes Later in Life due to a Novel Homozygous p.L171F ABCC8 Mutation | Emregül IŞIK,HÜSEYİN DEMİRBİLEK,Jayne A. HOUGHTON,Sian ELLARD,Sarah E FLANAGAN,Khalid HUSSAIN | 82–87 |
| Inherited Deletion of 1q, Hyperparathyroidism and Signs of Y-chromosomal Influence in a Patient with Turner Syndrome | Alejandro F. SILLER,Alex SHIMONY,Marwan SHINAWI,Ina AMARILLO,Louis P. DEHNER,Katherine SEMENKOVİCH,Ana María ARBELAEZ | 88–93 |
| Hyperphosphatemic Familial Tumoral Calcinosis in Two Siblings with a Novel Mutation in GALNT3 Gene: Experience from Southern Turkey | Rabia Miray KIŞLA EKİNCİ,FATİH GÜRBÜZ,Sibel BALCI,ATIL BİŞGİN,MEHMET TAŞTAN,BİLGİN YÜKSEL,Mustafa YILMAZ | 94–99 |
| Severe Neonatal Cholestasis as an Early Presentation of McCuneAlbright Syndrome | Nicole COLES,Ian COMEAU,Tatiana MUNOZ,Jennifer HARRINGTON,Roberto MENDOZA LONDONO,Andreas SCHULZE,Sari KIVES,Binita M. KAMATH,Jill HAMILTON | 100–103 |
| 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 | 104–108 |