Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
- 1 September 1991
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 14 (5) , 674-680
- https://doi.org/10.1007/bf01799932
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency: Identification of a new inborn error of mitochondrial fatty acidβ‐oxidationJournal of Inherited Metabolic Disease, 1990
- Retrospective diagnosis of 3-hydroxydicarboxylic aciduria by analysis of filter paper blood samplesJournal of Inherited Metabolic Disease, 1990
- 3-hydroxydicarboxylic aciduria—a fatty acid oxidation defect with severe prognosisThe Journal of Pediatrics, 1990
- SUDDEN INFANT DEATH AND LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASEThe Lancet, 1989
- Familial hypoketotic hypoglycaemia associated with peripheral neuropathy, pigmentary retinopathy and C6–C14 hydroxydicarboxylic aciduria. A new defect in fatty acid oxidation?Journal of Inherited Metabolic Disease, 1988
- 3-Hydroxyoctanoic aciduria: Identification of a new organic acid in the urine of a patient with non-ketotic hypoglycemiaClinica Chimica Acta; International Journal of Clinical Chemistry, 1988
- Peroxisomal β-oxidation of palmitoyl-CoA in human liver homogenates and its deficiency in the cerebro-hepato-renal (Zellweger) syndromeClinica Chimica Acta; International Journal of Clinical Chemistry, 1986
- A new case of C6–C14 dicarboxylic aciduria with favourable evolutionJournal of Inherited Metabolic Disease, 1986
- Age‐related differences in plasmalogen content of erythrocytes from patients with the cerebro‐hepato‐renal (Zellweger) syndrome: Implications for postnatal detection of the diseaseJournal of Inherited Metabolic Disease, 1985
- Urinary excretion of gamma-hydroxybutyric acid in a patient with neurological abnormalities. The probability of a new inborn error of metabolismClinica Chimica Acta; International Journal of Clinical Chemistry, 1981