Long-chain 3-hydroxyacyl-CoA dehydrogenase in leukocytes and chorionic villus fibroblasts: Potential for pre- and postnatal diagnosis
- 1 May 1992
- journal article
- Published by Springer Nature in Journal of Inherited Metabolic Disease
- Vol. 15 (3) , 356-358
- https://doi.org/10.1007/bf02435975
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyJournal of Inherited Metabolic Disease, 1991
- Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiencyThe Journal of Pediatrics, 1991
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase DeficiencyPediatric Research, 1991
- 3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatmentEuropean Journal of Pediatrics, 1991
- Deficiency of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase: A Cause of Lethal Myopathy and Cardiomyopathy in Early ChildhoodPediatric Research, 1990
- Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency: Identification of a new inborn error of mitochondrial fatty acidβ‐oxidationJournal of Inherited Metabolic Disease, 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
- 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