Disorders of glycogen and lipid metabolism

Adv Neurol. 1977:17:123-42.
No abstract available

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Adolescent
  • Adult
  • Carnitine O-Palmitoyltransferase / deficiency
  • Female
  • Glucosidases / deficiency
  • Glycogen Storage Disease / metabolism*
  • Glycogen Storage Disease Type II / enzymology
  • Glycogen Storage Disease Type II / metabolism
  • Glycogen Storage Disease Type III / metabolism
  • Glycogen Storage Disease Type IV / metabolism
  • Glycogen Storage Disease Type V / drug therapy
  • Glycogen Storage Disease Type V / metabolism
  • Glycogen Storage Disease Type V / physiopathology
  • Glycogen Storage Disease Type VII / enzymology
  • Glycogen Storage Disease Type VII / metabolism
  • Humans
  • Lactates / metabolism
  • Lipid Metabolism, Inborn Errors / drug therapy
  • Lipid Metabolism, Inborn Errors / metabolism*
  • Male
  • Muscle Contraction
  • Myoglobinuria / etiology
  • Phosphofructokinase-1 / deficiency

Substances

  • Lactates
  • Adenosine Triphosphate
  • Carnitine O-Palmitoyltransferase
  • Phosphofructokinase-1
  • Glucosidases