- 1. Seminoma in 46, XY Gonadal Dysgenesis: Rare Presentation and Review of the LiteratureMaamoun Adra, Hayato Nakanishi, Eleni Papachristodoulou, et al.
2024 · Volume 16 · Issue 4 · Pages 495–500
- 2. Treatment of Severe Hyperglycemia in Extremely Preterm Infants Using Continuous Subcutaneous Insulin TherapyMerle Böettger, Tony Zhou, Jennifer Knopp, et al.
2024 · Volume 16 · Issue 4 · Pages 443–449
- 3. Current Diagnostic Approaches in the Genetic Diagnosis of Disorders of Sex DevelopmentDeniz Özalp Kızılay, Samim Özen
2024 · Volume 16 · Issue 4 · Pages 401–410
- 4. Predictors and Trends of Diabetic Ketoacidosis at Diagnosis of Type 1 Diabetes Mellitus in Malaysian ChildrenMeenal Mavinkurve, Nurul Hanis Ramzi, Muhammad Yazid Bin Jalaludin, et al.
2024 · Volume 16 · Issue 4 · Pages 411–418
- 5. A Boy with Reset Osmostat Who Developed Chronic Hyponatremia due to Hypothalamic Injury Caused By a Giant Arachnoid CystJunko Naganuma, Satomi Koyama, Yoshiyuki Watabe, et al.
2024 · Volume 16 · Issue 4 · Pages 489–494
- 6. Molecular Genetic Diagnosis with Targeted Next Generation Sequencing in a Cohort of Turkish Osteogenesis Imperfecta Patients and their Genotype-phenotype CorrelationSamim Özen, Damla Gökşen, Ferda Evin, et al.
2024 · Volume 16 · Issue 4 · Pages 431–442
- 7. Novel OBSL1 Variant in a Chinese Patient with 3M Syndrome: The c.458dupG Mutation May Be a Potential Hotspot Mutation in the Chinese PopulationYurong Piao, Rongmin Li, Yingjie Wang, et al.
2024 · Volume 16 · Issue 4 · Pages 501–506
- 8. The Relationship Between Sleep Quality, Sleep Duration, Social Jet Lag and Obesity in AdolescentsFunda Yıldız, Melike Zeynep Tuğrul Aksakal, Raif Yıldız, et al.
2024 · Volume 16 · Issue 4 · Pages 419–425
- 9. Long-term Follow-up of a Late Diagnosed Patient with Temple SyndromeNikolinka Yordanova, Violeta Iotova, Deborah J. G. Mackay, et al.
2024 · Volume 16 · Issue 4 · Pages 475–480
- 10. Elemental Milk Formula as a Possible Cause of Hypophosphatemic Rickets in Wiedemann-Steiner SyndromeFahad Al-Juraibah, Maali Melha, Azam Alromaih, et al.
2024 · Volume 16 · Issue 3 · Pages 355–360
- 11. Clinical Presentation and Genetic Analysis of Neonatal 11β-Hydroxylase Deficiency Induced by a Chimeric CYP11B2/CYP11B1 GeneWenjuan Cai, Dan Yu, Jian Gao, et al.
2024 · Volume 16 · Issue 3 · Pages 372–378
- 12. Mitotically Active Follicular Nodule in Early Childhood: A Case Report with a Novel Mutation in the Thyroglobulin GeneSirmen Kızılcan Çetin, Zehra Aycan, Zeynep Şıklar, et al.
2024 · Volume 16 · Issue 3 · Pages 340–343
- 13. Sepsis-induced Pancytopenia in an Adolescent Girl with Thyroid Storm: A Case ReportQing Zhou, Li-Yong Zhang, Qing-Xian Fu, et al.
2024 · Volume 16 · Issue 3 · Pages 367–371
- 14. Stress Induced Hyperglycemia in Early Childhood as a Clue for the Diagnosis of NEUROD1-MODYNur Berna Çelik, Naz Güleray Lafcı, Şenay Savaş-Erdeve, et al.
2024 · Volume 16 · Issue 2 · Pages 218–223
- 15. Vitamin D Receptor Gene Polymorphisms with Type 1 Diabetes Risk: CorrespondenceHinpetch Daungsupawong, Viroj Wiwanitkit
2024 · Volume 16 · Issue 2 · Pages 243–243
- 16. Severe Growth Hormone Deficiency in an Indian Boy Caused by a Novel 6 kb Homozygous Deletion Spanning the GH1 GeneBasma Haris, Idris Mohammed, Umm-Kulthum Ismail Umlai, et al.
2024 · Volume 16 · Issue 2 · Pages 229–234
- 17. Juvenile Granulosa Cell Tumor Mimicking HAIR-AN in a 4-year-old: A Case ReportRachel Choe Kim, Ilya Goldberg, Trevor Van Brunt, et al.
2024 · Volume 16 · Issue 2 · Pages 200–204
- 18. Short Adult Height After Rapid-tempo Puberty: When is it too Late to Treat?Peter A. Lee
2024 · Volume 16 · Issue 2 · Pages 235–242
- 19. Serum Ghrelin and Glucagon-like Peptide 1 Levels in Children with Prader-Willi and Bardet-Biedl SyndromesDoğa Türkkahraman, Suat Tekin, Merve Güllü, et al.
2024 · Volume 16 · Issue 2 · Pages 146–150
- 20. Neurodevelopmental Outcome of Infants with Transient Hypothyroxinemia of Prematurity in a Newborn Intensive Care UnitErhan Aygün, Seda Yılmaz Semerci, Adviye Çakıl Sağlık, et al.
2024 · Volume 16 · Issue 1 · Pages 60–68
- 21. Seminoma in 46, XY Gonadal Dysgenesis: Rare Presentation and Review of the LiteratureMaamoun Adra, Hayato Nakanishi, Eleni Papachristodoulou, et al.
2024 · Volume 16 · Issue 4 · Pages 495–500
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