Very long chain acyl-coenzyme A dehydrogenase deficiency in two siblings: Evolution after prenatal diagnosis and prompt management
- 1 September 1997
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 131 (3) , 444-446
- https://doi.org/10.1016/s0022-3476(97)80073-x
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Novel fatty acid beta-oxidation enzymes in rat liver mitochondria. I. Purification and properties of very-long-chain acyl-coenzyme A dehydrogenase.Published by Elsevier ,2021
- Mitochondrial very long chain acyl-CoA dehydrogenase deficiency--a new disorder of fatty acid oxidation.Archives of Disease in Childhood: Fetal & Neonatal, 1995
- Purification of human very-long-chain acyl-coenzyme A dehydrogenase and characterization of its deficiency in seven patients.Journal of Clinical Investigation, 1995
- Rapid Diagnosis of Long Chain and Medium Chain Fatty Acid Oxidation Disorders Using LymphocytesAnnals of Clinical Biochemistry: International Journal of Laboratory Medicine, 1995
- Very long‐chain acyl coenzyme A dehydrogenase deficiency presenting with exercise‐induced myoglobinuriaNeurology, 1994
- Identification of Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency in Three Patients Previously Diagnosed with Long-Chain Acyl-CoA Dehydrogenase DeficiencyPediatric Research, 1993
- A Novel Disease with Deficiency of Mitochondrial Very-Long-Chain Acyl-CoA DehydrogenaseBiochemical and Biophysical Research Communications, 1993
- Very long chain acyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid oxidation in fibroblastsBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1993
- Beta-oxidation of long-chain fatty acids by human fibroblasts: Evidence for a novel long-chain acyl-coenzyme a dehydrogenaseBiochemical and Biophysical Research Communications, 1992