Hypoketonuric 3-hydroxydicarboxylic aciduria in five patients with glycogen storage disease

J Inherit Metab Dis. 1997 Jul;20(3):407-10. doi: 10.1023/a:1005354701187.
No abstract available

Publication types

  • Clinical Trial

MeSH terms

  • Cells, Cultured
  • Child, Preschool
  • Creatinine / urine
  • Dicarboxylic Acids / urine*
  • Fatty Acids / metabolism*
  • Fatty Acids / urine
  • Female
  • Fibroblasts / metabolism
  • Gas Chromatography-Mass Spectrometry
  • Glycogen Storage Disease / urine*
  • Humans
  • Infant
  • Liver / enzymology
  • Liver / pathology
  • Male
  • Oxidation-Reduction

Substances

  • Dicarboxylic Acids
  • Fatty Acids
  • Creatinine