All Stories

  1. A macrosomic preterm baby with hypoinsulinemic hypoketotic hypoglycemia: a diagnostic puzzle
  2. Author’s reply “Comment on diagnostic utility of the average peak LH levels measured during GnRH stimulation test”
  3. Managing Severe Hypoglycaemia in Patients with Diabetes: Current Challenges and Emerging Therapies
  4. Cystoscopy-Guided Laparoscopic Excision of Prostatic Utricle: Report of a Case
  5. Ion Transporters, Channelopathies, and Glucose Disorders
  6. Congenital hyperinsulinism and evolution to sulfonylurea-responsive diabetes later in life due to a novel homozygous p.L171F ABCC8 mutation
  7. Hyperinsulinaemic hypoglycaemia in children and adults
  8. Diagnosis and treatment of hyperinsulinaemic hypoglycaemia and its implications for paediatric endocrinology
  9. Severe Hypercalcemia in a Child With Acute Lymphoblastic Leukemia Relapse
  10. A novel ALMS1 homozygous mutation in two Turkish brothers with Alström syndrome
  11. 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
  12. Capillary Bedside Blood Glucose Measurement in Neonates: Missing a Diagnosis of Galactosemia
  13. Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study
  14. Prepubertal Unilateral Gynecomastia: Report of 2 Cases
  15. Familial Isolated Growth Hormone Deficiency Due to A Novel Homozygous Missense Mutation in the Growth Hormone Releasing Hormone Receptor Gene: Clinical Presentation With Hypoglycemia
  16. Normosmic idiopathic hypogonadotropic hypogonadism due to a novel homozygous nonsense c.C969A (p.Y323X) mutation in theKISS1Rgene in three unrelated families
  17. Long-Term Follow-Up of Children With Congenital Hyperinsulinism on Octreotide Therapy
  18. Pancreatic Endocrine and Exocrine Function in Children following Near-Total Pancreatectomy for Diffuse Congenital Hyperinsulinism
  19. Persistent hyperinsulinaemic hypoglycaemia in infancy
  20. Clinical characteristics and phenotype-genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations
  21. Multiple Pituitary Hormone Deficiency Due to Gunshot Injury in a 6-Year-Old Girl
  22. Incidence of Type 1 Diabetes Mellitus in Turkish Children from the Southeastern Region of the Country: A Regional Report
  23. Combined nutritional anemia coexisting with microcytic anemia
  24. Prevalence of type 1 diabetes mellitus in school children 6–18 years old in Diyarbakır, Southeastern Anatolian Region of Turkey
  25. Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism
  26. Hypophosphatasia Presenting with Pyridoxine-Responsive Seizures, Hypercalcemia, and Pseudotumor Cerebri: Case Report
  27. 17β-Hydroxysteroid dehydrogenase type 3 deficiency as a result of a homozygous 7 base pair deletion in 17βHSD3 gene
  28. Evaluation of serum kisspeptin levels in girls in the diagnosis of central precocious puberty and in the assessment of pubertal suppression
  29. Assessment of gonadotrophin suppression in girls treated with GnRH analogue for central precocious puberty; validity of single luteinizing hormone measurement after leuprolide acetate injection
  30. Giant virilizing adrenocortical carcinoma in a girl presenting with mutism
  31. GnRH Stimulation Test in Precocious Puberty: Single Sample is Adequate for Diagnosis and Dose Adjustment
  32. Two pediatric patients with Von Hippel-Lindau disease type 2b: from patient to screening, from screening to patient
  33. Anemia and Neutropenic Fever with High Dose Diazoxide Treatment in a Case with Hyperinsulinism due to Munchausen by Proxy
  34. Assessment of thyroid function during the long course of Hashimoto's thyroiditis in children and adolescents
  35. Hashimoto's Thyroiditis in Children and Adolescents: A Retrospective Study on Clinical, Epidemiological and Laboratory Properties of the Disease