Reversal of severe hypertrophic cardiomyopathy and excellent neuropsychologic outcome in very-long-chain acyl-coenzyme A dehydrogenase deficiency

This publication has 21 references indexed in Scilit:

• Catalytic and FAD-binding Residues of Mitochondrial Very Long Chain Acyl-Coenzyme A Dehydrogenase
  Journal of Biological Chemistry, 1998
• Mitochondrial very long chain acyl-CoA dehydrogenase deficiency--a new disorder of fatty acid oxidation.
  Archives of Disease in Childhood: Fetal & Neonatal, 1995
• Detection and assessment by positron emission tomography of a genetically determined defect in myocardial fatty acid utilization (long-chain acyl-coa dehydrogenase deficiency)
  The American Journal of Cardiology, 1993
• A Novel Disease with Deficiency of Mitochondrial Very-Long-Chain Acyl-CoA Dehydrogenase
  Biochemical and Biophysical Research Communications, 1993
• Very long chain acyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid oxidation in fibroblasts
  Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1993
• Fatty acid oxidation disorders: A new class of metabolic diseases
  The Journal of Pediatrics, 1992
• Clinical diagnosis of long-chain acyl-coenzyme A-dehydrogenase deficiency: Use of stress and fat-loading tests
  The Journal of Pediatrics, 1991
• Defect in fatty acid oxidation: Laboratory and pathologic findings in a patient
  Pediatric Neurology, 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 treatment
  European Journal of Pediatrics, 1991
• Prophylaxis of early ventricular fibrillation by inhibition of acylcarnitine accumulation.
  Journal of Clinical Investigation, 1989