E-ISSN: 1308-5735 ISSN: 1308-5727

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Volume 14, Issue 2

June 2022

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Original Article 8

Review

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

Original Article

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

İbrahim Mert Erbaş

Kübra Yüksek Acinikli

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

Umut Altunoğlu

Zehra Yavaş Abalı

Şükran Poyrazoğlu

Agharza Aghayev

Rüveyde Bundak

Feyza Darendeliler

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

Funda Feryal Taş

Huseyin Demirbilek

Mehmet Nuri Özbek

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

İbrahim Mert Erbaş

Ali Rıza Şişman

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

Güler Beyazgül

İlkay Yurtseven

Fulya Coşkunol

Gül İrem Kanberoğlu

Özlem Nalbantoğlu

The Role of American Thyroid Association Pediatric Thyroid Cancer Risk Stratification and BRAF^V600E Mutation in Predicting the Response to Treatment in Papillary Thyroid Cancer Patients ≤18 Years Old

Yasemin Giles Şenyürek

İsmail Cem Sormaz

Şükran Poyrazoğlu

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

Rüveyde Bundak

Zehra Yavaş Abalı

Feyza Darendeliler

Gülbin Gökçay

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

Feyza Darendeliler

Case Report

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

Nadia Schoenmakers

Adeline K. Nicholas

Orit Pinhas Hamiel

Yonatan Yeshayahu

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

Yael Levy-Shraga

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

Emine Çamtosun

Ayşehan Akıncı

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

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

Mohammed Ayed Huneif

Ziyad Hamad Alhazmy

Mohammed A. Alghofely

Aziza M. Mushiba

Abdulhamid Alsaheel

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

Mariola Iliszko

Beata S. Lipska-Zietkiewicz

Wojciech Kosiak

Ninela Irga-Jaworska

Ewa Izycka-Swieszewska