The diagnosis and biochemical investigation of a patient with a short chain fatty acid oxidation defect

Short-Chain Acyl-CoA Dehydrogenase Deficiency Associated with a Lipid-Storage Myopathy and Secondary Carnitine Deficiency

Douglass M. Turnbull, K. Bartlett, David L. Stevens et al. · New England Journal of Medicine · 1984 · 135 citations

Life Sciences, Biochemistry, Biochemical Genetics +13

Ethylmalonic-Adipic Aciduria

S Mantagos, Myron Genel, Kay Tanaka · Journal of Clinical Investigation · 1979 · 109 citations · Full text

Life Sciences, Biochemistry, Cellular Metabolism +15

Riboflavin‐responsive ethylmalonic—adipic aciduria

A. Green, T. Marshall, Michael J. Bennett et al. · Journal of Inherited Metabolic Disease · 1984 · 39 citations

Life Sciences, Biochemistry, Internal Medicine +13

Glutaric aciduria type II: Biochemical investigation and treatment of a child diagnosed prenatally

Michael J. Bennett, David Curnock, Paul C. Engel et al. · Journal of Inherited Metabolic Disease · 1983 · 36 citations

Medicine, Biochemistry, Pediatrics +4