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Journal Abstract Search

121 related items for PubMed ID: 9565984

  • 21. Arrhythmias and conduction defects as presenting symptoms of fatty acid oxidation disorders in children.
    Bonnet D, Martin D, Pascale De Lonlay, Villain E, Jouvet P, Rabier D, Brivet M, Saudubray JM.
    Circulation; 1999 Nov 30; 100(22):2248-53. PubMed ID: 10577999
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  • 22. Beta-oxidation of long-chain fatty acids by human fibroblasts: evidence for a novel long-chain acyl-coenzyme A dehydrogenase.
    Kelley RI.
    Biochem Biophys Res Commun; 1992 Feb 14; 182(3):1002-7. PubMed ID: 1540149
    [Abstract] [Full Text] [Related]

  • 23. Reversal of severe hypertrophic cardiomyopathy and excellent neuropsychologic outcome in very-long-chain acyl-coenzyme A dehydrogenase deficiency.
    Cox GF, Souri M, Aoyama T, Rockenmacher S, Varvogli L, Rohr F, Hashimoto T, Korson MS.
    J Pediatr; 1998 Aug 14; 133(2):247-53. PubMed ID: 9709714
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  • 24. Sudden child death and 'healthy' affected family members with medium-chain acyl-coenzyme A dehydrogenase deficiency.
    Duran M, Hofkamp M, Rhead WJ, Saudubray JM, Wadman SK.
    Pediatrics; 1986 Dec 14; 78(6):1052-7. PubMed ID: 3786030
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  • 25. Very-long-chain acyl-coenzyme a dehydrogenase deficiency in mice.
    Exil VJ, Roberts RL, Sims H, McLaughlin JE, Malkin RA, Gardner CD, Ni G, Rottman JN, Strauss AW.
    Circ Res; 2003 Sep 05; 93(5):448-55. PubMed ID: 12893739
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  • 26. Isolated mitochondrial myopathy associated with muscle coenzyme Q10 deficiency.
    Lalani SR, Vladutiu GD, Plunkett K, Lotze TE, Adesina AM, Scaglia F.
    Arch Neurol; 2005 Feb 05; 62(2):317-20. PubMed ID: 15710863
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  • 27. Very long chain acyl coenzyme A dehydrogenase deficiency in a 5-month-old Korean boy: identification of a novel mutation.
    Hahn SH, Lee EH, Jung JW, Hong CH, Yoon HR, Rinaldo P, Sims H, Gibson B, Strauss AW.
    J Pediatr; 1999 Aug 05; 135(2 Pt 1):250-3. PubMed ID: 10431122
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  • 31. Acute, severe cardiomyopathy as main symptom of late-onset very long-chain acyl-coenzyme A dehydrogenase deficiency.
    Parini R, Menni F, Garavaglia B, Fesslova V, Melotti D, Massone ML, Lamantea E, Rimoldi M, Vizziello P, Gatti R.
    Eur J Pediatr; 1998 Dec 05; 157(12):992-5. PubMed ID: 9877038
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  • 36. Genetic defects of acyl-CoA dehydrogenases: studies using an electron transfer flavoprotein reduction assay.
    Hale DE, Stanley CA, Coates PM.
    Prog Clin Biol Res; 1990 Dec 05; 321():333-48. PubMed ID: 2326298
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  • 37. Long-chain L-3-hydroxyacyl-coenzyme a dehydrogenase deficiency: a molecular and biochemical review.
    Rakheja D, Bennett MJ, Rogers BB.
    Lab Invest; 2002 Jul 05; 82(7):815-24. PubMed ID: 12118083
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  • 39. A simple spectrophotometric assay for long-chain acyl-CoA dehydrogenase activity measurements in human skin fibroblasts.
    Ijlst L, Wanders RJ.
    Ann Clin Biochem; 1993 May 05; 30 ( Pt 3)():293-7. PubMed ID: 8517612
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