Ganglioside storage diseases: an updated review

Ital J Neurol Sci. 1981 Aug;2(3):219-26. doi: 10.1007/BF02335401.
No abstract available

Publication types

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

MeSH terms

  • Adolescent
  • Brain Diseases, Metabolic / diagnosis
  • Child
  • Child, Preschool
  • Clinical Enzyme Tests
  • Female
  • G(M1) Ganglioside
  • G(M2) Ganglioside
  • Gangliosidoses / enzymology
  • Gangliosidoses / genetics
  • Gangliosidoses / metabolism
  • Gangliosidoses / physiopathology*
  • Humans
  • Infant
  • Infant, Newborn
  • Isoenzymes / metabolism
  • Mass Screening
  • Metabolism, Inborn Errors / enzymology
  • Models, Genetic
  • Phenotype
  • Pregnancy
  • Prenatal Diagnosis
  • Sandhoff Disease / pathology
  • Tay-Sachs Disease / pathology
  • Tay-Sachs Disease / physiopathology
  • beta-Galactosidase / metabolism

Substances

  • Isoenzymes
  • G(M2) Ganglioside
  • G(M1) Ganglioside
  • beta-Galactosidase