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Published/Copyright: February 9, 2024

Published Online: 2024-02-09
Published in Print: 2024-02-26

©2024 Walter de Gruyter GmbH, Berlin/Boston

Articles in the same Issue

  1. Frontmatter
  2. Review
  3. Myoinositol or D-chiro-inositol for PCOS symptoms in adolescents: a narrative review
  4. Mini Review
  5. Effects of the COVID-19 pandemic on the incidence of central precocious puberty; a narrative review
  6. Original Articles
  7. Evaluation of the role of FTO (rs9939609) and MC4R (rs17782313) gene polymorphisms in type 1 diabetes and their relation to obesity
  8. Lack of association between month of birth and risk of developing type 1 diabetes in Brazil: a 40-year analysis
  9. Review on the screening of urine glucose for early diagnosis of type 2 diabetes mellitus in school children and adolescents with obesity in Hong Kong
  10. Effect of daily zinc supplementation for 12 weeks on serum thyroid auto-antibody levels in children and adolescents with autoimmune thyroiditis – a randomized controlled trial
  11. Correlation between serum vitamin D level and uterine volume in girls with idiopathic central precocious puberty
  12. Diagnostic model based on multiple factors for girls with central precocious puberty
  13. Validity and reliability of parent assessments of pubertal maturation among adolescent girls in Isfahan, Iran
  14. Newborn screening for primary carnitine deficiency using a second-tier genetic test
  15. Case Reports
  16. From neglect to peril: diabetic ketoacidosis unleashing colonic necrosis and perforation in an adolescent girl with type 1 diabetes mellitus
  17. Unusual onset of Graves’ disease associated with thymic hyperplasia in a 5-year-old girl with congenital bilateral clinical anophthalmia: diagnostic and therapeutic challenges
  18. Thyroid hormone resistance and large goiter mimicking infiltrative carcinoma in a pediatric patient
  19. Hereditary hypomagnesemia with secondary hypocalcemia caused by a novel mutation in TRPM6 gene
  20. Letter to the Editor
  21. Congenital hyperinsulinism patient with ABCC8 and KCNJ11 double heterozygous variants: a case report with 6 years follow-up
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