Ions and genes in persistent hyperinsulinaemic hypoglycaemia in infancy: a commentary on the implications for tailoring treatment to disease pathogenesis

J Pediatr Endocrinol Metab. 1998 Mar:11 Suppl 1:121-9. doi: 10.1515/jpem.1998.11.s1.121.
No abstract available

Publication types

  • Case Reports
  • Review

MeSH terms

  • Cells, Cultured
  • DNA Mutational Analysis
  • Female
  • Humans
  • Hyperinsulinism / complications
  • Hyperinsulinism / congenital
  • Hyperinsulinism / genetics*
  • Hyperinsulinism / therapy*
  • Hypoglycemia / complications
  • Hypoglycemia / congenital
  • Hypoglycemia / genetics*
  • Hypoglycemia / therapy*
  • Infant, Newborn
  • Islets of Langerhans / physiopathology