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Published/Copyright: August 3, 2019

Published Online: 2019-08-03
Published in Print: 2019-08-27

©2019 Walter de Gruyter GmbH, Berlin/Boston

Articles in the same Issue

  1. Frontmatter
  2. Mini Review
  3. Endocrine manifestations of PHACE syndrome
  4. Original Articles
  5. Quantitation of the arginine family amino acids in the blood of full-term infants perinatally in relation to their birth weight
  6. Effect of supplementation with omega-3 fatty acids on hypertriglyceridemia in pediatric patients with obesity
  7. Pediatric diabetes inpatient care: can medical staff knowledge be improved?
  8. Association of lipid profile and BMI Z-score in southern Iranian children and adolescents
  9. Arterial stiffness in children and adolescents with and without continuous insulin infusion
  10. Fasting during the holy month of Ramadan among older children and adolescents with type 1 diabetes in Kuwait
  11. Evaluation of the relationship between short-term glycemic control and netrin-1, a urinary proximal tubular injury marker in children with type 1 diabetes
  12. Incidence of diabetic ketoacidosis in newly diagnosed type 1 diabetes children in western Saudi Arabia: 11-year experience
  13. Novel mutations and spectrum of the disease of NR0B1 (DAX1)-related adrenal insufficiency in Indian children
  14. Metabolic profile, cardiovascular risk factors and health-related quality of life in children, adolescents and young adults with congenital adrenal hyperplasia
  15. Safety and effectiveness of growth hormone therapy in infants with Prader-Willi syndrome younger than 2 years: a prospective study
  16. Response to sapropterin hydrochloride (Kuvan®) in children with phenylketonuria (PKU): a clinical trial
  17. Prophylactic thyroidectomy in multiple endocrine neoplasia type 2A in children: a single centre experience
  18. Benign thyroid nodules in pediatric patients: determining best practices for repeat ultrasound evaluations
  19. Letter to the Editor
  20. Thyroid function in males with fragile X syndrome
  21. Case Reports
  22. A case of a severe reaction following the use of bisphosphonates in a patient with osteogenesis imperfecta
  23. Cushing disease in a patient with nonbullous congenital ichthyosiform erythroderma: lessons in avoiding glucocorticoids in ichthyosis
  24. Contiguous gene deletion in a Chinese family with X-linked nephrogenic diabetes insipidus: challenges in early diagnosis and implications for affected families
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