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PUBMED FOR HANDHELDS

Journal Abstract Search


292 related items for PubMed ID: 2824921

  • 21. Aspects of long-chain acyl-COA metabolism.
    Tol VA.
    Mol Cell Biochem; 1975 Apr 30; 7(1):19-31. PubMed ID: 1134497
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  • 23. Mitochondrial myopathies. Clinical, morphological and biochemical aspects.
    Sengers RC, Stadhouders AM, Trijbels JM.
    Eur J Pediatr; 1984 Feb 30; 141(4):192-207. PubMed ID: 6329761
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  • 24. Molecular defects of NADH-ubiquinone oxidoreductase (complex I) in mitochondrial diseases.
    Morgan-Hughes JA, Schapira AH, Cooper JM, Clark JB.
    J Bioenerg Biomembr; 1988 Jun 30; 20(3):365-82. PubMed ID: 3136150
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  • 25. [Abnormality in the mitochondrial energy-producing system].
    Ozawa T, Tanaka M.
    Tanpakushitsu Kakusan Koso; 1988 Apr 30; 33(5):824-7. PubMed ID: 2855955
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  • 26. Partial deficiency of complexes I and IV of the mitochondrial respiratory chain in skeletal muscle of two patients with mitochondrial myopathy.
    Bleistein J, Zierz S.
    J Neurol; 1989 May 30; 236(4):218-22. PubMed ID: 2547913
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  • 27. Clinical presentation of mitochondrial respiratory chain defects in NADH-coenzyme Q reductase and cytochrome oxidase: clues to pathogenesis of Leigh disease.
    Robinson BH, De Meirleir L, Glerum M, Sherwood G, Becker L.
    J Pediatr; 1987 Feb 30; 110(2):216-22. PubMed ID: 3027293
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  • 29. Blue native polyacrylamide gel electrophoresis: a powerful tool in diagnosis of oxidative phosphorylation defects.
    Van Coster R, Smet J, George E, De Meirleir L, Seneca S, Van Hove J, Sebire G, Verhelst H, De Bleecker J, Van Vlem B, Verloo P, Leroy J.
    Pediatr Res; 2001 Nov 30; 50(5):658-65. PubMed ID: 11641463
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  • 30. The control of mitochondrial oxidations by complex III in rat muscle and liver mitochondria. Implications for our understanding of mitochondrial cytopathies in man.
    Taylor RW, Birch-Machin MA, Bartlett K, Lowerson SA, Turnbull DM.
    J Biol Chem; 1994 Feb 04; 269(5):3523-8. PubMed ID: 8106394
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  • 33. [Neurological approach to mitochondrial abnormalities].
    Yokochi K.
    No To Hattatsu; 1987 Mar 04; 19(2):118-24. PubMed ID: 3030378
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  • 34. Deficiency of the reduced nicotinamide adenine dinucleotide dehydrogenase component of complex I of mitochondrial electron transport. Fatal infantile lactic acidosis and hypermetabolism with skeletal-cardiac myopathy and encephalopathy.
    Hoppel CL, Kerr DS, Dahms B, Roessmann U.
    J Clin Invest; 1987 Jul 04; 80(1):71-7. PubMed ID: 3110216
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  • 36. Expression of oxidative phosphorylation genes in muscle cell cultures from patients with mitochondrial myopathies.
    Collombet JM, Faure-Vigny H, Mandon G, Dumoulin R, Boissier S, Bernard A, Mousson B, Stepien G.
    Mol Cell Biochem; 1997 Mar 04; 168(1-2):73-85. PubMed ID: 9062896
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  • 40. [A case of mitochondrial encephalomyopathy with a defect in electron transport at complex I and IV in skeletal muscle showing peripheral neuropathy].
    Ohnishi A, Nakano S, Hashimoto T, Tsuji S, Murai Y.
    Rinsho Shinkeigaku; 1988 Jan 04; 28(1):107-11. PubMed ID: 2838209
    [No Abstract] [Full Text] [Related]


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