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Volumn 15, Issue 8, 2000, Pages 1232-1234

Very-long-chain acyl-coenzyme A dehydrogenase deficiency - A new cause of myoglobinuric acute renal failure

Author keywords

Acute renal failure; Acylcarnitines; Myoglobinuria; Rhabdomyolysis; Very long chain acyl coenzyme A dehydrogenase deficiency

Indexed keywords

ACYL COENZYME A DEHYDROGENASE; MYOGLOBIN;

EID: 0033930733     PISSN: 09310509     EISSN: None     Source Type: Journal    
DOI: 10.1093/ndt/15.8.1232     Document Type: Article
Times cited : (7)

References (8)
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    • Vianey-Saban C, Divry P, Brivet M et al. Mitochondrial very-long-chain acyl coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patients. Clin Chim Acta 1998; 269: 43-62
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    • Vianey-Saban, C.1    Divry, P.2    Brivet, M.3
  • 2
    • 0030070639 scopus 로고    scopus 로고
    • Rhabdomyolysis and myohemoglobinuric acute renal failure
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    • Zager, R.A.1
  • 3
    • 0026518372 scopus 로고
    • Novel fatty acid B-oxidation enzymes in rat liver mitochondria. I. Purification and properties of very-long-chain acyl-coenzyme A dehydrogenase
    • Izai K, Uchida Y, Orii T, Yamamoto S, Hashimoto T. Novel fatty acid B-oxidation enzymes in rat liver mitochondria. I. Purification and properties of very-long-chain acyl-coenzyme A dehydrogenase. J Biol Chem 1992; 267: 1027-1033
    • (1992) J Biol Chem , vol.267 , pp. 1027-1033
    • Izai, K.1    Uchida, Y.2    Orii, T.3    Yamamoto, S.4    Hashimoto, T.5
  • 4
    • 0029881587 scopus 로고    scopus 로고
    • Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD gene
    • Andresen BS, Bross P, Vianey-Saban C et al. Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD gene. Hum Mol Genet 1996; 5: 461-472
    • (1996) Hum Mol Genet , vol.5 , pp. 461-472
    • Andresen, B.S.1    Bross, P.2    Vianey-Saban, C.3
  • 5
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    • Genomic DNA organisation of human mitochondrial very-long-chain acyl-CoA dehydrogenase and mutation analysis
    • Orii KO, Aoyama T, Souri M et al. Genomic DNA organisation of human mitochondrial very-long-chain acyl-CoA dehydrogenase and mutation analysis. Biochim Biophys Res Commun 1995; 217: 987-992
    • (1995) Biochim Biophys Res Commun , vol.217 , pp. 987-992
    • Orii, K.O.1    Aoyama, T.2    Souri, M.3
  • 6
    • 0011597369 scopus 로고    scopus 로고
    • VLCAD deficiency presenting with recurrent rhabdomyolysis in an adult
    • abstract
    • Gillett GT, Krywawych S, Brivet M et al. VLCAD Deficiency presenting with recurrent rhabdomyolysis in an adult. J Inher Metab Dis 1996; 19 [Suppl. 54]: 108 [abstract]
    • (1996) J Inher Metab Dis , vol.19 , Issue.SUPPL. 54 , pp. 108
    • Gillett, G.T.1    Krywawych, S.2    Brivet, M.3
  • 7
    • 0028221809 scopus 로고
    • Very long-chain acyl cocnzyme A dehydrogenase deficiency presenting with exercise-induced myoglobinuria
    • Ogilvie I, Pourfarzam M, Jackson S, Stockdale C, Bartlett K, Turnbull DM. Very long-chain acyl cocnzyme A dehydrogenase deficiency presenting with exercise-induced myoglobinuria. Neurology 1994; 44: 467-473
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    • Ogilvie, I.1    Pourfarzam, M.2    Jackson, S.3    Stockdale, C.4    Bartlett, K.5    Turnbull, D.M.6
  • 8
    • 0031798837 scopus 로고    scopus 로고
    • Very long chain acyl-coenzyme A dehydrogenase deficiency with adult onset
    • Smelt AHM, Poorthuis BJHM, Okenhout W et al. Very long chain acyl-coenzyme A dehydrogenase deficiency with adult onset. Ann Neurol 1998; 43: 540-544
    • (1998) Ann Neurol , vol.43 , pp. 540-544
    • Smelt, A.H.M.1    Poorthuis, B.J.H.M.2    Okenhout, W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.