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Journal Abstract Search

177 related items for PubMed ID: 11596343

  • 1. [Complex II (succinate-ubiquinone reductase) deficiency].
    Nonaka I.
    Ryoikibetsu Shokogun Shirizu; 2001; (36):132-4. PubMed ID: 11596343
    [No Abstract] [Full Text] [Related]

  • 2. [Complex II deficiency due to Fp gene mutation].
    Ito M.
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():444-5. PubMed ID: 12013908
    [No Abstract] [Full Text] [Related]

  • 3. [Abnormality in the mitochondrial energy-producing system].
    Ozawa T, Tanaka M.
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):824-7. PubMed ID: 2855955
    [No Abstract] [Full Text] [Related]

  • 4. Phenotypic dichotomy in mitochondrial complex II genetic disorders.
    Baysal BE, Rubinstein WS, Taschner PE.
    J Mol Med (Berl); 2001 Sep; 79(9):495-503. PubMed ID: 11692162
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  • 13. Biochemical investigations and immunoblot analyses of two unrelated patients with an isolated deficiency in complex II of the mitochondrial respiratory chain.
    Birch-Machin MA, Marsac C, Ponsot G, Parfait B, Taylor RW, Rustin P, Munnich A.
    Biochem Biophys Res Commun; 1996 Mar 07; 220(1):57-62. PubMed ID: 8602857
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  • 14. Mutations in SDHC cause autosomal dominant paraganglioma, type 3.
    Niemann S, Müller U.
    Nat Genet; 2000 Nov 07; 26(3):268-70. PubMed ID: 11062460
    [Abstract] [Full Text] [Related]

  • 15. [Optic atrophy and ataxia (complex II deficiency-mutation in Fp subunit gene of succinate dehydrogenase)].
    Goto Y.
    Nihon Rinsho; 2002 Apr 07; 60 Suppl 4():376-7. PubMed ID: 12013890
    [No Abstract] [Full Text] [Related]

  • 16. [From gene to disease; from SDHD, a defect in the respiratory chain, to paragangliomas and pheochromocytomas].
    Taschner PE, Bröcker-Vriends AH, van der Mey AG.
    Ned Tijdschr Geneeskd; 2002 Nov 16; 146(46):2188-90. PubMed ID: 12467161
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  • 17. 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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  • 18. 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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  • 19. [Succinate-ubiquinone reductase site of the respiratory chain].
    Vinogradov AD.
    Biokhimiia; 1986 Dec 17; 51(12):1944-73. PubMed ID: 3542059
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  • 20. 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 17; 39(2):224-32. PubMed ID: 8967754
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