| 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 | 131–144 |
| 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 | 145–152 |
| 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 | 153–171 |
| 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 | 172–178 |
| 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 | 179–187 |
| 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 | 188–195 |
| 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 | 196–206 |
| 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 | 207–215 |
| 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 | 216–220 |
| 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 | 221–226 |
| TRMT10A Mutation in a Child with Diabetes, Short Stature, Microcephaly and Hypoplastic Kidneys | Ortal BAREL, Eve STERN, Asaf VİVANTE, Yael Levy-SHRAGA | 227–232 |
| 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 | 233–238 |
| 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 | 239–243 |
| 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 | 244–250 |
| 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 | 251–257 |