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Year | Number of Results |
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1985 | 1 |
1987 | 1 |
1990 | 1 |
2024 | 0 |
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Clinical and biochemical variation and family studies in the multiple acyl-CoA dehydrogenation disorders.
Pediatr Res. 1987 Apr;21(4):371-6. doi: 10.1203/00006450-198704000-00010.
Pediatr Res. 1987.
PMID: 3574988
Screening for inborn errors of fatty acid oxidation in cultured fibroblasts: an overview.
Rhead WJ.
Rhead WJ.
Prog Clin Biol Res. 1990;321:365-82.
Prog Clin Biol Res. 1990.
PMID: 2183237
Review.
No abstract available.
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Catalytic defect of medium-chain acyl-coenzyme A dehydrogenase deficiency. Lack of both cofactor responsiveness and biochemical heterogeneity in eight patients.
Amendt BA, Rhead WJ.
Amendt BA, et al.
J Clin Invest. 1985 Sep;76(3):963-9. doi: 10.1172/JCI112096.
J Clin Invest. 1985.
PMID: 3840178
Free PMC article.
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