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PUBMED FOR HANDHELDS

Journal Abstract Search

139 related items for PubMed ID: 8602857

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  • 2. Deficiency of complex II of the mitochondrial respiratory chain in late-onset optic atrophy and ataxia.
    Taylor RW, Birch-Machin MA, Schaefer J, Taylor L, Shakir R, Ackrell BA, Cochran B, Bindoff LA, Jackson MJ, Griffiths P, Turnbull DM.
    Ann Neurol; 1996 Feb; 39(2):224-32. PubMed ID: 8967754
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  • 3. Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency.
    Bourgeron T, Rustin P, Chretien D, Birch-Machin M, Bourgeois M, Viegas-Péquignot E, Munnich A, Rötig A.
    Nat Genet; 1995 Oct; 11(2):144-9. PubMed ID: 7550341
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  • 11. Inborn errors of complex II--unusual human mitochondrial diseases.
    Rustin P, Rötig A.
    Biochim Biophys Acta; 2002 Jan 17; 1553(1-2):117-22. PubMed ID: 11803021
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  • 12. Partial deficiency of subunits in complex I or IV of patients with mitochondrial myopathies.
    Tanaka M, Nishikimi M, Suzuki H, Ozawa T, Koga Y, Nonaka I.
    Biochem Int; 1987 Mar 17; 14(3):525-30. PubMed ID: 2884999
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  • 13. Mitochondrial disorders of the nervous system: clinical, biochemical, and molecular genetic features.
    Thyagarajan D, Byrne E.
    Int Rev Neurobiol; 2002 Mar 17; 53():93-144. PubMed ID: 12512338
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  • 14. Late-onset optic atrophy, ataxia, and myopathy associated with a mutation of a complex II gene.
    Birch-Machin MA, Taylor RW, Cochran B, Ackrell BA, Turnbull DM.
    Ann Neurol; 2000 Sep 17; 48(3):330-5. PubMed ID: 10976639
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  • 15. [Optic atrophy and ataxia (complex II deficiency-mutation in Fp subunit gene of succinate dehydrogenase)].
    Goto Y.
    Nihon Rinsho; 2002 Apr 17; 60 Suppl 4():376-7. PubMed ID: 12013890
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  • 18. 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 17; 62(2):317-20. PubMed ID: 15710863
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