Fatty acid β-oxidation deficiency masquerading as fulminant myocarditis
Authors:
- 1 August 1998
- journal article
- case report
- Published by Elsevier in International Journal of Cardiology
- Vol. 65 (3) , 287-289
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Efficiency of metabolic screening in childhood cardiomyopathiesEuropean Heart Journal, 1998
- Genomic DNA Organization of Human Mitochondrial Very-Long-Chain Acyl-CoA Dehydrogenase and Mutation AnalysisBiochemical and Biophysical Research Communications, 1995
- Disorders of mitochondrial long‐chain fatty acid oxidationJournal of Inherited Metabolic Disease, 1995
- Purification of human very-long-chain acyl-coenzyme A dehydrogenase and characterization of its deficiency in seven patients.Journal of Clinical Investigation, 1995
- Genetic disorders of mitochondrial fatty acid oxidationCurrent Opinion in Pediatrics, 1994
- Inherited CardiomyopathiesNew England Journal of Medicine, 1994
- A Clinicopathologic Description of MyocarditisClinical Immunology and Immunopathology, 1993
- Clinicopathoiogic description of myocarditisJACC, 1991
- Deficiency of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase: A Cause of Lethal Myopathy and Cardiomyopathy in Early ChildhoodPediatric Research, 1990
- Defects of metabolism of fatty acids in the sudden infant death syndrome.BMJ, 1985