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Short chain acyl-coenzyme A dehydrogenase (SCAD) deficiency: immunochemical demonstration of molecular heterogeneity due to variant SCAD with differing stabilityNAITO, E; INDO, Y; TANAKA, K et al.The Journal of clinical investigation. 1989, Vol 84, Num 5, pp 1671-1674, issn 0021-9738, 4 p.Article

Immunoprecipitation and electrophoretic analysis of four human acyl-CoA dehydrogenases and electron transfer flavoprotein using antibodies raised against the corresponding rat enzymesIKEDA, Y; TANAKA, K.Biochemical medicine and metabolic biology. 1987, Vol 37, Num 3, pp 329-334, issn 0885-4505Article

Synthesis of enantiomerically pure [(methylenecyclopropyl)acetyl]-CoA : the causative agent of jamaican vomiting sicknessMING-TAIN LAI; OH, E; SHIH, Y et al.Journal of organic chemistry. 1992, Vol 57, Num 8, pp 2471-2476, issn 0022-3263Article

Determination of medium chain acyl-CoA dehydrogenase activity in cultured skin fibroblasts using mass spectrometryNIEZEN-KONING, K. E; CHAPMAN, T. E; MULDER, I. E et al.Clinica chimica acta. 1991, Vol 199, Num 2, pp 173-184, issn 0009-8981Article

New evidence supporting a radical mechanism of the inactivation of general acyl-CoA dehydrogenase by a metabolite of hypoglycinMING-TAIN LAI; HUNG-WEN LIU.Journal of the American Chemical Society. 1992, Vol 114, Num 8, pp 3160-3162, issn 0002-7863Article

Studies of the inactivation of general acyl-CoA dehydrogenase by racemic (methylenecyclopropyl)acetyl-CoA: new evidence suggesting a radical mechanism of this enzyme-catalyzed reactionLENN, N. D; SHIH, Y; STANKOVICH, M. T et al.Journal of the American Chemical Society. 1989, Vol 111, Num 8, pp 3065-3067, issn 0002-7863, 3 p.Article

Molecular pathogenesis of a novel mutation, G108D, in short-chain acyl-CoA dehydrogenase identified in subjects with short-chain acyl-CoA dehydrogenase deficiencySHIRAO, Kenichiro; OKADA, Satoshi; TAKIHARA, Yoshihiro et al.Human genetics. 2010, Vol 127, Num 6, pp 619-628, issn 0340-6717, 10 p.Article

Perioperative management of a child with short-chain acyl-CoA dehydrogenase deficiencyTURPIN, Brian; TOBIAS, Joseph D.Paediatric anaesthesia (Paris). 2005, Vol 15, Num 9, pp 771-777, issn 1155-5645, 7 p.Article

Diagnosis of medium chain acyl CoA dehydrogenase deficiency by measurement of cis-4-decenoic acid in dried blood spotsHEALES, S. J. R; LEONARD, J. V.Clinica chimica acta. 1992, Vol 209, Num 1-2, pp 61-66, issn 0009-8981Article

Studies of the inactivation of general acyl-coa dehydrogenase by (1r)- and (1s)-(methylenecyclopropyl)acetyl-coaMING-TAIN LAI; OH, E; HUNG-WEN LIU et al.Bioorganic & medicinal chemistry letters. 1992, Vol 2, Num 11, pp 1423-1426Article

Characterization of a disease-causing Lys329 to Glu mutation in 16 patients with medium-chain Acyl-CoA dehydrogenase deficiencyGREGERSEN, N; ANDRESEN, B. S; KØLVRAA, S et al.Journal of inherited metabolic disease. 1991, Vol 14, Num 3, pp 314-316, issn 0141-8955Article

Intramitochondrial fatty acid metabolism : riboflavin deficiency and energy productionPARSONS, H. G; DIAS, V. C.Biochemistry and cell biology. 1991, Vol 69, Num 7, pp 490-497, issn 0829-8211Conference Paper

Neonatal onset of medium-chain acyl-CoA dehydrogenase deficiency in two siblingsNOBUKUNI, Y; YOKOO, T; OHTANI, Y et al.Brain & development (Tokyo. 1979). 1988, Vol 10, Num 2, pp 129-134, issn 0387-7604Article

Biochemical Correction of Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency After Portal Vein Injection of rAAV8-SCADBEATTIE, Stuart G; GOETZMAN, Eric; CONLON, Thomas et al.Human gene therapy. 2008, Vol 19, Num 6, pp 579-588, issn 1043-0342, 10 p.Article

Analysis of polymerase chain reaction-product by capillary electrophoresis with laser-induced fluorescence detection and its application to the diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiencyARAKAWA, H; UETANAKA, K; MAEDA, M et al.Journal of chromatography. A. 1994, Vol 680, Num 2, pp 517-523Conference Paper

Hyperuricemia in medium-chain acyl-coenzyme A dehydrogenase deficiencyDAVIDSON-MUNDT, A; LUDER, A. S; GREENE, C. L et al.The Journal of pediatrics. 1992, Vol 120, Num 3, pp 444-446, issn 0022-3476Article

Impaired tetramer assembly of variant medium-chain acyl-coenzyme A dehydrogenase with a glutamate or aspartate substitution for lysine 304 causing instability of the proteinYOKOTA, I; SAIJO, T; VOCKLEY, J et al.The Journal of biological chemistry (Print). 1992, Vol 267, Num 36, pp 26004-26010, issn 0021-9258Article

A new simple screening method for the diagnosis of medium chain acyl-CoA dehydrogenase deficiencyBHUIYAN, A. K. M. J; WATMOUGH, N. J; TURNBULL, D. M et al.Clinica chimica acta. 1987, Vol 165, Num 1, pp 39-44, issn 0009-8981Article

Lethal multiple acyl-CoA dehydrogenation deficiency with dysmorphic featuresBENNETT, M. J; POLLITT, R. J; LAND, J. M et al.Journal of inherited metabolic disease. 1987, Vol 10, Num 1, pp 95-96, issn 0141-8955Article

Purification and properties of short chain acyl-CoA, medium chain acyl-CoA, and isovaleryl-CoA dehydrogenases from human liverFINOCCHIARO, G; ITO, M; TANAKA, K et al.The Journal of biological chemistry (Print). 1987, Vol 262, Num 17, pp 7982-7989, issn 0021-9258Article

The measurement of carnitine and acyl-carnitines : applications to the investigation of patients with suspected inherited disorders of mitochondrial fatty acid oxidationBHUIYAN, A. K. M. J; JACKSON, S; TURNBULL, D. M et al.Clinica chimica acta. 1992, Vol 207, Num 3, pp 185-204, issn 0009-8981Article

Frequency of the G985 MCAD mutation in the general populationBLAKEMORE, A. I. F; SINGLETON, H; POLLITT, R. J et al.Lancet (British edition). 1991, Vol 337, Num 8736, pp 298-299, issn 0140-6736, 2 p.Article

Molecular survey of a prevalent mutation, ⁹⁸⁵A-to-G transition, and identification of five infrequent mutations in the medium-chain acyl-CoA dehydrogenase (MCAD) gene in 55 patients with MCAD deficiencyYOKOTA, I; COATES, P. M; HALE, D. E et al.American journal of human genetics. 1991, Vol 49, Num 6, pp 1280-1291, issn 0002-9297Article

Vitreous humour organic acids in medium chain acyl-CoA dehyudrogenase deficiencyMILLS, G. A; WALKER, V; ASHTON, M. R et al.Journal of inherited metabolic disease. 1990, Vol 13, Num 2, pp 239-240, issn 0141-8955, 2 p.Article