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Published/Copyright: September 8, 2018

Published Online: 2018-09-08
Published in Print: 2018-09-25

©2018 Walter de Gruyter GmbH, Berlin/Boston

Articles in the same Issue

  1. Frontmatter
  2. Original Articles
  3. Intracranial pathologies associated with central diabetes insipidus in infants
  4. Omentin-1 and NAMPT serum concentrations are higher and CK-18 levels are lower in children and adolescents with type 1 diabetes when compared to healthy age, sex and BMI matched controls
  5. Evaluation of anthropometric parameters of central obesity in Pakistani children aged 5–12 years, using receiver operating characteristic (ROC) analysis
  6. A lower energetic, protein and uncooked cornstarch intake is associated with a more severe outcome in glycogen storage disease type III: an observational study of 50 patients
  7. Untreated congenital hypothyroidism due to loss to follow-up: developing preventive strategies through quality improvement
  8. The effect of 17 years of increased salt iodization on the prevalence and nature of goiter in Croatian schoolchildren
  9. Is there an association between thyrotropin levels within the normal range and birth growth parameters in full-term newborns?
  10. Etiology of short stature in Indian children and an assessment of the growth hormone-insulin-like growth factor axis in children with idiopathic short stature
  11. Growth of patients with congenital adrenal hyperplasia due to 21-hydroxylase in infancy, glucocorticoid requirement and the role of mineralocorticoid therapy
  12. A personal series of 100 children operated for Cushing’s disease (CD): optimizing minimally invasive diagnosis and transnasal surgery to achieve nearly 100% remission including reoperations
  13. 12-Week aerobic exercise and nutritional program minimized the presence of the 64Arg allele on insulin resistance
  14. Letter to the Editor
  15. Successful treatment of life-threatening severe metabolic acidosis by continuous veno-venous hemodialysis in a child with diabetic ketoacidosis
  16. Case Reports
  17. Two siblings with metachromatic leukodystrophy caused by a novel identified homozygous mutation in the ARSA gene
  18. To diet or not to diet in neonatal diabetes responding to sulfonylurea treatment
  19. Van Wyk-Grumbach syndrome with hemangioma in an infant
  20. Maternal iodine excess: an uncommon cause of acquired neonatal hypothyroidism
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