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Published/Copyright: January 6, 2017

Published Online: 2017-1-6
Published in Print: 2017-1-1

©2017 Walter de Gruyter GmbH, Berlin/Boston

Articles in the same Issue

  1. Frontmatter
  2. Editorial
  3. Disorders of sex development
  4. Original Articles
  5. Fertility and sexual function: a gap in training in pediatric endocrinology
  6. Disorders of sex development in children in KwaZulu-Natal Durban South Africa: 20-year experience in a tertiary centre
  7. Novel mutations of the SRD5A2 and AR genes in Thai patients with 46, XY disorders of sex development
  8. Sensitivity and specificity of different methods for cystic fibrosis-related diabetes screening: is the oral glucose tolerance test still the standard?
  9. Anti-hyperglycemic activity of Aegle marmelos (L.) corr. is partly mediated by increased insulin secretion, α-amylase inhibition, and retardation of glucose absorption
  10. Risk factors that affect metabolic health status in obese children
  11. Nocturnal levels of chemerin and progranulin in adolescents: influence of sex, body mass index, glucose metabolism and sleep
  12. Elevated endogenous secretory receptor for advanced glycation end products (esRAGE) levels are associated with circulating soluble RAGE levels in diabetic children
  13. Food exchange estimation by children with type 1 diabetes at summer camp
  14. Usefulness of non-fasting lipid parameters in children
  15. Monitoring steroid replacement therapy in children with congenital adrenal hyperplasia
  16. Clinical and molecular characterization of Beckwith-Wiedemann syndrome in a Chinese population
  17. An analysis of the sequence of the BAD gene among patients with maturity-onset diabetes of the young (MODY)
  18. Case Reports
  19. Hypogonadotropic hypogonadism in a female patient with congenital arhinia
  20. Transdermal testosterone gel for induction and continuation of puberty in adolescent boys with hepatic dysfunction
  21. Long-term response to growth hormone therapy in a patient with short stature caused by a novel heterozygous mutation in NPR2
  22. Three cases of Japanese acromicric/geleophysic dysplasia with FBN1 mutations: a comparison of clinical and radiological features
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