Pompe disease in infants and children

J Pediatr. 2004 May;144(5 Suppl):S35-43. doi: 10.1016/j.jpeds.2004.01.053.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adult
  • Child, Preschool
  • Female
  • Glycogen Storage Disease Type II / diagnosis
  • Glycogen Storage Disease Type II / drug therapy
  • Glycogen Storage Disease Type II / physiopathology
  • Humans
  • Infant
  • Male
  • alpha-Glucosidases / deficiency
  • alpha-Glucosidases / metabolism
  • alpha-Glucosidases / therapeutic use*

Substances

  • alpha-Glucosidases