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• The multiple acyl-coenzyme A dehydrogenation disorders, glutaric aciduria type II and ethylmalonic-adipic aciduria. Mitochondrial fatty acid oxidation, acyl-coenzyme A dehydrogenase, and electron transfer flavoprotein activities in fibroblasts.

  Amendt BA, Rhead WJ. Amendt BA, et al. J Clin Invest. 1986 Jul;78(1):205-13. doi: 10.1172/JCI112553. J Clin Invest. 1986. PMID: 3722376 Free PMC article.
• The inborn errors of mitochondrial fatty acid oxidation.

  Vianey-Liaud C, Divry P, Gregersen N, Mathieu M. Vianey-Liaud C, et al. J Inherit Metab Dis. 1987;10 Suppl 1:159-200. doi: 10.1007/BF01812855. J Inherit Metab Dis. 1987. PMID: 3119938 Review.
• Primary lipid cardiomyopathy.

  Zimmermann A, Wyss P, Stocker F. Zimmermann A, et al. Virchows Arch A Pathol Anat Histopathol. 1990;416(5):453-9. doi: 10.1007/BF01605153. Virchows Arch A Pathol Anat Histopathol. 1990. PMID: 2107634 Review.
• Short-chain acyl-coenzyme A dehydrogenase deficiency. Clinical and biochemical studies in two patients.

  Amendt BA, Greene C, Sweetman L, Cloherty J, Shih V, Moon A, Teel L, Rhead WJ. Amendt BA, et al. J Clin Invest. 1987 May;79(5):1303-9. doi: 10.1172/JCI112953. J Clin Invest. 1987. PMID: 3571488 Free PMC article.
• Deficiency of electron transfer flavoprotein or electron transfer flavoprotein:ubiquinone oxidoreductase in glutaric acidemia type II fibroblasts.

  Frerman FE, Goodman SI. Frerman FE, et al. Proc Natl Acad Sci U S A. 1985 Jul;82(13):4517-20. doi: 10.1073/pnas.82.13.4517. Proc Natl Acad Sci U S A. 1985. PMID: 2989828 Free PMC article.