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Frontmatter

Published/Copyright: November 30, 2021

Published Online: 2021-11-30
Published in Print: 2021-12-20

©2021 Walter de Gruyter GmbH, Berlin/Boston

Articles in the same Issue

  1. Frontmatter
  2. Review Article
  3. Calcitonin and complementary biomarkers in the diagnosis of hereditary medullary thyroid carcinoma in children and adolescents
  4. Original Articles
  5. Genotype and phenotypic spectrum of vitamin D dependent rickets type 1A: our experience and systematic review
  6. Questioning the adequacy of standardized vitamin D supplementation protocol in very low birth weight infants: a prospective cohort study
  7. Growth hormone replacement therapy: is it safe to use in children with asymptomatic pituitary lesions?
  8. Comparing adolescent self staging of pubertal development with hormone biomarkers
  9. Reverse circadian glucocorticoid treatment in prepubertal children with congenital adrenal hyperplasia
  10. The concordance between ultrasonographic stage of breast and Tanner stage of breast for overweight and obese girls: a school population-based study
  11. Cross-sectional analysis: clinical presentation of children with persistently low ALP levels
  12. The utility of continuous glucose monitoring systems in the management of children with persistent hypoglycaemia
  13. Long-term effect of conventional phosphate and calcitriol treatment on metabolic recovery and catch-up growth in children with PHEX mutation
  14. Role of magnetic resonance diffusion weighted imaging in diagnosis of diabetic nephropathy in children living with type 1 diabetes mellitus
  15. Investigation of quality of life in obese adolescents: the effect of psychiatric symptoms of obese adolescent and/or mother on quality of life
  16. Predictive value of WHO vs. IAP BMI charts for identification of metabolic risk in Indian children and adolescents
  17. Case Reports
  18. COVID-19 triggered encephalopathic crisis in a patient with glutaric aciduria type 1
  19. Aromatase deficiency in an Ontario Old Order Mennonite family
  20. A case of monogenic diabetes mellitus caused by a novel heterozygous RFX6 nonsense mutation in a 14-year-old girl
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