Bilateral Ovarian Germ Cell Tumor in a 46,XX Female with Nijmegen Breakage Syndrome and Hypergonadotropic Hypogonadism

Malgorzata A. KRAWCZYK, Malgorzata STYCZEWSKA, Dorota BİRKHOLZ-WALERZAK, Mariola ILISZKO, Beata S. LİPSKA-ZIETKIEWİCZ, Wojciech KOSİAK, Ninela IRGA-JAWORSKA, Ewa IZYCKA-SWIESZEWSKA, Ewa BIEN

A Novel Mutation in the Thyroglobulin Gene Resulting in Neonatal Goiter and Congenital Hypothyroidism in an Eritrean Infant

Nadia SCHOENMAKERS, Adeline K. NICHOLAS, Eran KASSİF, Orit Pinhas HAMIEL, Eve STERN, Yonatan YESHAYAHU

A Novel SCNN1A Variation in a Patient with Autosomal-recessive Pseudohypoaldosteronism Type 1

Mohammed Ayed HUNEİF, Ziyad Hamad ALHAZMY, Aziza M. MUSHİBA, Anas M. SHOOMİ, Mohammed A. ALGHOFELY, Abdulhamid ALSAHEEL, Humariya HEENA

Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD

Feyza DARENDELİLER, Neşe AKÇAN, Rüveyde BUNDAK, Şükran POYRAZOĞLU, Zehra YAVAŞ ABAK, Şahin AVCI, Güven TOKSOY, Umut ALTUNOĞLU, Birsen KARAMAN, Seher BAŞARAN, Agharza AGHAEV, Volkan KARAMAN, Oya UYGUNER

A 4-hour Profile of 17-hydroxyprogesterone in Salt-wasting Congenital Adrenal Hyperplasia: Is the Serial Monitoring Strategy Worth the Effort?

Özge BEŞÇİ, İbrahim Mert ERBAŞ, Tuncay KÜME, Ece BÖBER, Kübra YÜKSEK ACINIKLI, Korcan DEMİR, Ayhan ABACI

Low Complement C1q/TNF-related Protein-13 Levels are Associated with Childhood Obesity But not Binge Eating Disorder

Serkan TURAN, Ahu PAKETÇİ, İbrahim Mert ERBAŞ, Ali Rıza ŞİŞMAN, Ece BÖBER, Korcan DEMİR, Ayhan ABACI

How Vitamin D Levels of Children Changed During COVID-19 Pandemic: A Comparison of Pre-pandemic and Pandemic Periods

Behzat ÖZKAN, Özlem BAĞ, Güler BEYAZGÜL, Gül İrem KANBEROĞLU, İlkay YURTSEVEN, Fulya COŞKUNOL, Saynur BAŞER, Duygu ÇİÇEK, Filiz ÇELİK, Özlem NALBANTOĞLU

The Impact of the CEDD-NET on the Evaluation of Rare Disorders: A Multicenter Scientific Research Platform in the Field of Pediatric Endocrinology

Feyza DARENDELİLER, Samim ÖZEN, Aysun ATA

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

Şükran POYRAZOĞLU, İsmail Cem SORMAZ, Yalın İŞCAN, Fatih TUNCA, Yasemin Giles ŞENYÜREK

46,XY Sex Development Defect due to a Novel Homozygous (Splice Site) c.673_1G>C Variation in the HSD17B3 Gene: Case Report

Leman KAYAŞ, Ayşehan AKINCI, Emine ÇAMTOSUN, Nurdan ÇİFTÇİ

Comparison of National Growth Standards for Turkish Infants and Children with World Health Organization Growth Standards

Olcay NEYZİ, Andrzej FURMAN, Feyza DARENDELİLER, Rüveyde BUNDAK, Hülya GÜNÖZ, Gülbin GÖKÇAY, Firdevs BAŞ, Zehra YAVAŞ ABALI

Efficacy and Safety of Letrozole in the Management of Constitutional Delay in Growth and Puberty: A Systematic Review and Meta-analysis

Meha SHARMA, Deep DUTTA, Rajiv SINGLA, Vineet SURANA

TRMT10A Mutation in a Child with Diabetes, Short Stature, Microcephaly and Hypoplastic Kidneys

Ortal BAREL, Eve STERN, Asaf VİVANTE, Yael Levy-SHRAGA

Revisiting the Annual Incidence of Type 1 Diabetes Mellitus in Children from the Southeastern Anatolian Region of Turkey: A Regional Report

Selma TUNÇ, Ruken YILDIRIM, Funda Feryal TAŞ, Mehmet Nuri ÖZBEK, Şervan ÖZALKAK, Hüseyin DEMİRBİLEK, Edip ÜNAL

The Successful Treatment of Deep Soft-tissue Calcifications with Topical Sodium Thiosulphate and Acetazolamide in a Boy with Hyperphosphatemic Familial Tumoral Calcinosis due to a Novel Mutation in FGF23

Hakan DÖNERAY, Ayşe ÖZDEN, Kadri GÜRBÜZ