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Journal Abstract Search

121 related items for PubMed ID: 9565984

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  • 4. Very-long-chain acyl-coenzyme A dehydrogenase deficiency--a new cause of myoglobinuric acute renal failure.
    Cairns AP, O'Donoghue PM, Patterson VH, Brown JH.
    Nephrol Dial Transplant; 2000 Aug; 15(8):1232-4. PubMed ID: 10910451
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  • 6. Mitochondrial trifunctional protein deficiency associated with recurrent myoglobinuria in adolescence.
    Miyajima H, Orii KE, Shindo Y, Hashimoto T, Shinka T, Kuhara T, Matsumoto I, Shimizu H, Kaneko E.
    Neurology; 1997 Sep; 49(3):833-7. PubMed ID: 9305349
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  • 11. Very long-chain acyl coenzyme A dehydrogenase deficiency presenting with exercise-induced myoglobinuria.
    Ogilvie I, Pourfarzam M, Jackson S, Stockdale C, Bartlett K, Turnbull DM.
    Neurology; 1994 Mar; 44(3 Pt 1):467-73. PubMed ID: 8145917
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  • 12. Genetic deficiency of medium-chain acyl coenzyme A dehydrogenase: studies in cultured skin fibroblasts and peripheral mononuclear leukocytes.
    Coates PM, Hale DE, Stanley CA, Corkey BE, Cortner JA.
    Pediatr Res; 1985 Jul; 19(7):671-6. PubMed ID: 4022673
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  • 16. Very long chain acyl-coenzyme A dehydrogenase deficiency in two siblings: evolution after prenatal diagnosis and prompt management.
    Sluysmans T, Tuerlinckx D, Hubinont C, Verellen-Dumoulin C, Brivet M, Vianey-Saban C.
    J Pediatr; 1997 Sep; 131(3):444-6. PubMed ID: 9329424
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  • 20. A heterozygous missense mutation in adolescent-onset very long-chain acyl-CoA dehydrogenase deficiency with exercise-induced rhabdomyolysis.
    Hisahara S, Matsushita T, Furuyama H, Tajima G, Shigematsu Y, Imai T, Shimohama S.
    Tohoku J Exp Med; 2015 Apr; 235(4):305-10. PubMed ID: 25843429
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