Do criteria exist from urinary organic acids to distinguish ?-oxidation defects?
- 1 January 1995
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 18 (2) , 257-260
- https://doi.org/10.1007/bf00711782
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Regulation of fatty acid oxidation in cellsBiochemical Society Transactions, 1994
- Secondary 3‐hydroxydicarboxylic aciduria mimicking long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiencyJournal of Inherited Metabolic Disease, 1994
- Ethylmalonic aciduria associated with progressive neurological disease and partial cytochromec oxidase deficiencyJournal of Inherited Metabolic Disease, 1993
- Muscle cytochrome c oxidase deficiency accompanied by a urinary organic acid pattern mimicking multiple acyl‐CoA dehydrogenase deficiencyJournal of Inherited Metabolic Disease, 1993
- Urinary 3-hydroxydicarboxylic acids in pathophysiology of metabolic disorders with dicarboxylic aciduriaMetabolism, 1991
- Influence of valproic acid on hepatic carbohydrate and lipid metabolismArchives of Biochemistry and Biophysics, 1983
- Biochemical studies in a patient with defects in the metabolism of acyl‐CoA and sarcosine: Another possible case of glutaric aciduria type IIJournal of Inherited Metabolic Disease, 1980