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PUBMED FOR HANDHELDS

Journal Abstract Search


153 related items for PubMed ID: 8145917

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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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  • 3. Medium-chain and long-chain acyl CoA dehydrogenase deficiency: clinical, pathologic and ultrastructural differentiation from Reye's syndrome.
    Treem WR, Witzleben CA, Piccoli DA, Stanley CA, Hale DE, Coates PM, Watkins JB.
    Hepatology; 1986 Apr; 6(6):1270-8. PubMed ID: 3793003
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  • 4. A novel disease with deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenase.
    Aoyama T, Uchida Y, Kelley RI, Marble M, Hofman K, Tonsgard JH, Rhead WJ, Hashimoto T.
    Biochem Biophys Res Commun; 1993 Mar 31; 191(3):1369-72. PubMed ID: 8466512
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  • 5. Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse.
    Cox KB, Hamm DA, Millington DS, Matern D, Vockley J, Rinaldo P, Pinkert CA, Rhead WJ, Lindsey JR, Wood PA.
    Hum Mol Genet; 2001 Sep 15; 10(19):2069-77. PubMed ID: 11590124
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  • 6. Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patients.
    Vianey-Saban C, Divry P, Brivet M, Nada M, Zabot MT, Mathieu M, Roe C.
    Clin Chim Acta; 1998 Jan 12; 269(1):43-62. PubMed ID: 9498103
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  • 7. The acyl-CoA dehydrogenation deficiencies. Recent advances in the enzymic characterization and understanding of the metabolic and pathophysiological disturbances in patients with acyl-CoA dehydrogenation deficiencies.
    Gregersen N.
    Scand J Clin Lab Invest Suppl; 1985 Jan 12; 174():1-60. PubMed ID: 3892650
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  • 8. Complementation analysis of fatty acid oxidation disorders.
    Moon A, Rhead WJ.
    J Clin Invest; 1987 Jan 12; 79(1):59-64. PubMed ID: 3793932
    [Abstract] [Full Text] [Related]

  • 9. Immunochemical characterization of variant long-chain acyl-CoA dehydrogenase in cultured fibroblasts from nine patients with long-chain acyl-CoA dehydrogenase deficiency.
    Indo Y, Coates PM, Hale DE, Tanaka K.
    Pediatr Res; 1991 Sep 12; 30(3):211-5. PubMed ID: 1945557
    [Abstract] [Full Text] [Related]

  • 10. Very long-chain acyl-CoA dehydrogenase deficiency presenting as acute hypercapnic respiratory failure.
    Tong MK, Lam CS, Mak TW, Fu MY, Ng SH, Wanders RJ, Tang NL.
    Eur Respir J; 2006 Aug 12; 28(2):447-50. PubMed ID: 16880373
    [Abstract] [Full Text] [Related]

  • 11. Immunochemical characterization of variant medium-chain acyl-CoA dehydrogenase in fibroblasts from patients with medium-chain acyl-CoA dehydrogenase deficiency.
    Coates PM, Indo Y, Young D, Hale DE, Tanaka K.
    Pediatr Res; 1992 Jan 12; 31(1):34-8. PubMed ID: 1594327
    [Abstract] [Full Text] [Related]

  • 12. Combined enzyme defect of mitochondrial fatty acid oxidation.
    Jackson S, Kler RS, Bartlett K, Briggs H, Bindoff LA, Pourfarzam M, Gardner-Medwin D, Turnbull DM.
    J Clin Invest; 1992 Oct 12; 90(4):1219-25. PubMed ID: 1401059
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  • 14. Altered Energetics of Exercise Explain Risk of Rhabdomyolysis in Very Long-Chain Acyl-CoA Dehydrogenase Deficiency.
    Diekman EF, Visser G, Schmitz JP, Nievelstein RA, de Sain-van der Velden M, Wardrop M, Van der Pol WL, Houten SM, van Riel NA, Takken T, Jeneson JA.
    PLoS One; 2016 Oct 12; 11(2):e0147818. PubMed ID: 26881790
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  • 16. The effect of dantrolene sodium in Very Long Chain Acyl-CoA Dehydrogenase Deficiency.
    Voermans NC, Poels PJ, Kluijtmans LA, van Engelen BG.
    Neuromuscul Disord; 2005 Dec 12; 15(12):844-6. PubMed ID: 16288870
    [Abstract] [Full Text] [Related]

  • 17. Rhabdomyolysis caused by an inherited metabolic disease: very long-chain acyl-CoA dehydrogenase deficiency.
    Voermans NC, van Engelen BG, Kluijtmans LA, Stikkelbroeck NM, Hermus AR.
    Am J Med; 2006 Feb 12; 119(2):176-9. PubMed ID: 16443431
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  • 20. Catalytic defect of medium-chain acyl-coenzyme A dehydrogenase deficiency. Lack of both cofactor responsiveness and biochemical heterogeneity in eight patients.
    Amendt BA, Rhead WJ.
    J Clin Invest; 1985 Sep 12; 76(3):963-9. PubMed ID: 3840178
    [Abstract] [Full Text] [Related]


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