All Stories

  1. Novel mutations in the LRP5 gene in patients with Osteoporosis-pseudoglioma syndrome
  2. The endocrine disruptor bisphenol A may play a role in the aetiopathogenesis of polycystic ovary syndrome in adolescent girls
  3. Premature thelarche related to fennel tea consumption?
  4. Endocrine abnormalities of patients with cleft lip and/or cleft palate during the neonatal period
  5. The Effects of Growth Hormone on Metabolic Changes and Quality of Life
  6. Iodine deficiency: a probable cause of neural tube defect
  7. Aortic Intima-Media Thickness in Newborns with Congenital Hypothyroidism
  8. Fatty liver is a good indicator of subclinical atherosclerosis risk in obese children and adolescents regardless of liver enzyme elevation
  9. The association of polythelia with segmentation defects of the vertebrae
  10. Congenital Hypothyroidism Due To Maternal Radioactive Iodine Exposure During Pregnancy
  11. A case of diabetes mellitus associated with Rett Syndrome
  12. Follow-Up During Early Infancy of Newborns Diagnosed with Subcutaneous Fat Necrosis
  13. Post-Operative Subcutaneous Fat Necrosis in a Newborn: A Case Report
  14. Pituitary duplication: a rare cause of precocious puberty
  15. Does Early Treatment Prevent Deafness in Thiamine-Responsive Megaloblastic Anaemia Syndrome?
  16. A Novel Mutation in the MC2R Gene Causing Familial Glucocorticoid Deficiency Type 1
  17. Vitamin D Deficiency Rickets Mimicking Pseudohypoparathyroidism-Case Report
  18. Familial Glucocorticoid Deficiency Type 2: A Case Report - Case Report
  19. Iodine Overload and Severe Hypothyroidism in Two Neonates
  20. Primary adrenal failure due to viral infection in an infant
  21. Melnick-Needles Syndrome Associated with Growth Hormone Deficiency: A Case Report
  22. Therapeutic Approach to Obesity in Children and Adolescents