Review
Efficacy and Safety of Letrozole in the Management of Constitutional Delay in Growth and Puberty: A Systematic Review and Meta-analysis
Deep Dutta, Rajiv Singla, Vineet Surana, et al.
Original Article
A 4-hour Profile of 17-hydroxyprogesterone in Salt-wasting Congenital Adrenal Hyperplasia: Is the Serial Monitoring Strategy Worth the Effort?
Özge Besci, İbrahim Mert Erbaş, Tuncay Küme, et al.
Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD
Neşe Akcan, Oya Uyguner, Firdevs Baş, et al.
Revisiting the Annual Incidence of Type 1 Diabetes Mellitus in Children from the Southeastern Anatolian Region of Turkey: A Regional Report
Şervan Özalkak, Ruken Yıldırım, Selma Tunç, et al.
Low Complement C1q/TNF-related Protein-13 Levels are Associated with Childhood Obesity But not Binge Eating Disorder
İbrahim Mert Erbaş, Ahu Paketçi, Serkan Turan, et al.
How Vitamin D Levels of Children Changed During COVID-19 Pandemic: A Comparison of Pre-pandemic and Pandemic Periods
Güler Beyazgül, Özlem Bağ, İlkay Yurtseven, et al.
The Role of American Thyroid Association Pediatric Thyroid Cancer Risk Stratification and BRAFV600E Mutation in Predicting the Response to Treatment in Papillary Thyroid Cancer Patients ≤18 Years Old
Yasemin Giles Şenyürek, Yalın İşcan, İsmail Cem Sormaz, et al.
Comparison of National Growth Standards for Turkish Infants and Children with World Health Organization Growth Standards
Rüveyde Bundak, Zehra Yavaş Abalı, Andrzej Furman, et al.
The Impact of the CEDD-NET on the Evaluation of Rare Disorders: A Multicenter Scientific Research Platform in the Field of Pediatric Endocrinology
Samim Özen, Aysun Ata, Feyza Darendeliler
Case Report
A Novel Mutation in the Thyroglobulin Gene Resulting in Neonatal Goiter and Congenital Hypothyroidism in an Eritrean Infant
Eve Stern, Nadia Schoenmakers, Adeline K. Nicholas, et al.
TRMT10A Mutation in a Child with Diabetes, Short Stature, Microcephaly and Hypoplastic Kidneys
Eve Stern, Asaf Vivante, Ortal Barel, et al.
46,XY Sex Development Defect due to a Novel Homozygous (Splice Site) c.673_1G>C Variation in the HSD17B3 Gene: Case Report
Nurdan Çiftci, Leman Kayaş, Emine Çamtosun, et al.
A Novel SCNN1A Variation in a Patient with Autosomal-recessive Pseudohypoaldosteronism Type 1
Mohammed Ayed Huneif, Ziyad Hamad Alhazmy, Anas M. Shoomi, et al.
Bilateral Ovarian Germ Cell Tumor in a 46,XX Female with Nijmegen Breakage Syndrome and Hypergonadotropic Hypogonadism
Malgorzata A. Krawczyk, Malgorzata Styczewska, Dorota Birkholz-Walerzak, et al.
