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acyl- CoA
Summary
General Info
Curated Studies
Most Correlated Studies
OMIM - Congenital disorder
OMIM - Metabolic disease
Mouse Phenotypes - Disorder of peroxisomal function
OMIM - Peroxisomal fatty acyl-CoA reductase 1 disorder
Livers of medium-chain acyl-coenzyme A dehydrgenase (MCAD) KO mice upon LPS treatment with fasting
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Literature
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Very long-chain acyl-CoA dehydrogenase deficiency and type I diabetes mellitus: Case report and mana…
Analysis of clinical characteristics and ACADM gene variants in four children with Medium chain acyl…
Medium-chain acyl-CoA dehydrogenase deficiency (MCADD) precipitating unexpected death in an infant: …
Free carnitine concentrations and biochemical parameters in medium-chain acyl-CoA dehydrogenase defi…
Personalised modelling of clinical heterogeneity between medium-chain acyl-CoA dehydrogenase patient…
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Effect of Bezafibrate on Muscle Metabolism in Patients With Fatty Acid Oxidation Defects
Use of Ravictiâ„¢ in Patients With MCAD Deficiency With the 985A>G (K304E) Mutation
Fatty Acid Oxidation Defects and Insulin Sensitivity
Long-Chain Fatty Acid Oxidation Disorders (LC-FAOD) Extension Study for Subjects Previously Enrolled…
Systemic Biomarkers of Brain Injury From Hyperammonemia
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