Disorders of Fatty Acid Oxidation

This publication has 19 references indexed in Scilit:

• Medium-Chain Acyl-CoA Dehydrogenase Deficiency
  New England Journal of Medicine, 1988
• Cis-4-decenoic acid in plasma: a characteristic metabolite in medium-chain acyl-CoA dehydrogenase deficiency.
  Clinical Chemistry, 1988
• Genetic deficiency of short-chain acyl-coenzyme A dehydrogenase in cultured fibroblasts from a patient with muscle carnitine deficiency and severe skeletal muscle weakness.
  Journal of Clinical Investigation, 1988
• Deficiency of electron transfer flavoprotein or electron transfer flavoprotein:ubiquinone oxidoreductase in glutaric acidemia type II fibroblasts.
  Proceedings of the National Academy of Sciences, 1985
• Genetic Deficiency of Medium-Chain Acyl Coenzyme A Dehydrogenase: Studies in Cultured Skin Fibroblasts and Peripheral Mononuclear Leukocytes
  Pediatric Research, 1985
• Long-Chain Acyl Coenzyme A Dehydrogenase Deficiency: An Inherited Cause of Nonketotic Hypoglycemia
  Pediatric Research, 1985
• Diagnostic and Therapeutic Implications of Medium-Chain Acylcarnitines in the Medium-Chain Acyl-CoA Dehydrogenase Deficiency
  Pediatric Research, 1985
• Medium-Chain Acyl-CoA Dehydrogenase Deficiency in Children with Non-Ketotic Hypoglycemia and Low Carnitine Levels
  Pediatric Research, 1983
• In vitro fibroblast studies in a patient with C6-C10-dicarboxylic aciduria: evidence for a defect in general acyl-CoA dehydrogenase
  Clinica Chimica Acta; International Journal of Clinical Chemistry, 1982
• Intermittent non‐ketotic dicarboxylic aciduria in two siblings with hypoglycaemia: An apparent defect in β‐oxidation of fatty acids
  Journal of Inherited Metabolic Disease, 1979