All Stories

  1. Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations
  2. Capillary Bedside Blood Glucose Measurement in Neonates: Missing a Diagnosis of Galactosemia
  3. Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study
  4. Prepubertal Unilateral Gynecomastia: Report of 2 Cases
  5. Familial Isolated Growth Hormone Deficiency Due to A Novel Homozygous Missense Mutation in the Growth Hormone Releasing Hormone Receptor Gene: Clinical Presentation With Hypoglycemia
  6. Normosmic idiopathic hypogonadotropic hypogonadism due to a novel homozygous nonsense c.C969A (p.Y323X) mutation in theKISS1Rgene in three unrelated families
  7. Long-Term Follow-Up of Children With Congenital Hyperinsulinism on Octreotide Therapy
  8. Pancreatic Endocrine and Exocrine Function in Children following Near-Total Pancreatectomy for Diffuse Congenital Hyperinsulinism
  9. Persistent hyperinsulinaemic hypoglycaemia in infancy
  10. Clinical characteristics and phenotype-genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations
  11. Multiple Pituitary Hormone Deficiency Due to Gunshot Injury in a 6-Year-Old Girl
  12. Incidence of Type 1 Diabetes Mellitus in Turkish Children from the Southeastern Region of the Country: A Regional Report
  13. Combined nutritional anemia coexisting with microcytic anemia
  14. Prevalence of type 1 diabetes mellitus in school children 6–18 years old in Diyarbakır, Southeastern Anatolian Region of Turkey
  15. Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism
  16. Hypophosphatasia Presenting with Pyridoxine-Responsive Seizures, Hypercalcemia, and Pseudotumor Cerebri: Case Report
  17. 17β-Hydroxysteroid dehydrogenase type 3 deficiency as a result of a homozygous 7 base pair deletion in 17βHSD3 gene
  18. Evaluation of serum kisspeptin levels in girls in the diagnosis of central precocious puberty and in the assessment of pubertal suppression
  19. Assessment of gonadotrophin suppression in girls treated with GnRH analogue for central precocious puberty; validity of single luteinizing hormone measurement after leuprolide acetate injection
  20. Giant virilizing adrenocortical carcinoma in a girl presenting with mutism
  21. GnRH Stimulation Test in Precocious Puberty: Single Sample is Adequate for Diagnosis and Dose Adjustment
  22. Two pediatric patients with Von Hippel-Lindau disease type 2b: from patient to screening, from screening to patient
  23. Anemia and Neutropenic Fever with High Dose Diazoxide Treatment in a Case with Hyperinsulinism due to Munchausen by Proxy
  24. Assessment of thyroid function during the long course of Hashimoto's thyroiditis in children and adolescents
  25. Unilocular Cystic Hydatidosis in Breast
  26. Hashimoto's Thyroiditis in Children and Adolescents: A Retrospective Study on Clinical, Epidemiological and Laboratory Properties of the Disease