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Diagnosis of adrenal insufficiency in children: a survey among pediatric endocrinologists in North America

This erratum corrects the original online version which can be found here: https://doi.org/10.1515/jpem-2022-0444
  • Carolina Silva , Trisha Patel and Carol Lam EMAIL logo
Published/Copyright: June 12, 2023

Published Online: 2023-06-12
Published in Print: 2023-07-26

© 2023 Walter de Gruyter GmbH, Berlin/Boston

Articles in the same Issue

  1. Frontmatter
  2. Review Article
  3. Molecular mechanisms involved in fetal programming and disease origin in adulthood
  4. Original Articles
  5. Neuropathy in paediatric type 1 diabetes mellitus – clinical characterization and analysis of risk factors in the diabetes prospective follow-up registry DPV (Diabetes-Patienten-Verlaufsdokumentation)-registry
  6. Effect of metabolic control on cognitive functions in children and adolescents with type 1 diabetes mellitus
  7. Uric acid and sCD163 as biomarkers for metabolic dysfunction and MAFLD in children and adolescents with overweight and obesity
  8. Endocrinological, immunological and metabolic features of patients with Fabry disease under therapy
  9. Evaluation and management of pediatric thyroid nodules and thyroid cancer at a single institution after adoption of the American Thyroid Association 2015 guidelines
  10. Fasting ketone levels vary by age: implications for differentiating physiologic from pathologic ketotic hypoglycemia
  11. Association of adipocytokines and adipocytokine ratios with cardiovascular risk factors in Japanese preadolescents
  12. Daily vs. monthly oral vitamin D3 for treatment of symptomatic vitamin D deficiency in infants: a randomized controlled trial
  13. Short Communication
  14. Management and outcomes in secondary diabetes among pediatric patients hospitalized with hemophagocytic lymphohistiocytosis
  15. Letter to the Editor
  16. Potential usefulness of assessing serum betamethasone levels during betamethasone therapy
  17. Case Reports
  18. Acquired idiopathic isolated ACTH deficiency with associated autoimmune thyroiditis in pediatrics: case report and review of the literature
  19. A very rare cause of hypertrygliseridemia in infancy: a novel mutation in glycerol-3-phosphate dehydrogenase 1 (GPD1) gene
  20. Difficult to think about but easy to treat: scurvy
  21. Severe hypophosphataemia can be an early sign of osteopetrorickets: a case report
  22. Corrigendum
  23. Diagnosis of adrenal insufficiency in children: a survey among pediatric endocrinologists in North America
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