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Journal Abstract Search

122 related items for PubMed ID: 2846961

  • 1. Cytochrome c oxidase deficiency in three patients with Leigh's disease.
    Di Rocco M, Veneselli E, Ciccone MO, Taccone A, Stroppiano M, Cottafava F.
    J Inherit Metab Dis; 1988; 11 Suppl 2():189-92. PubMed ID: 2846961
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  • 2. Biochemical study in 28 children with lactic acidosis, in relation to Leigh's encephalomyelopathy.
    Miyabayashi S, Ito T, Narisawa K, Iinuma K, Tada K.
    Eur J Pediatr; 1985 Mar; 143(4):278-83. PubMed ID: 2985393
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  • 6. Cytochrome c oxidase deficiency in subacute necrotizing encephalopathy (Leigh syndrome).
    Hayasaka K, Brown GK, Danks DM, Droste M, Kadenbach B.
    J Inherit Metab Dis; 1989 Mar; 12(3):247-56. PubMed ID: 2559245
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  • 9. Biochemical and molecular analysis of cytochrome c oxidase deficiency in Leigh's syndrome.
    Lombes A, Nakase H, Tritschler HJ, Kadenbach B, Bonilla E, DeVivo DC, Schon EA, DiMauro S.
    Neurology; 1991 Apr; 41(4):491-8. PubMed ID: 1849240
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  • 13. Cytochrome c oxidase deficiency and long-chain acyl coenzyme A dehydrogenase deficiency with Leigh's subacute necrotizing encephalomyelopathy.
    Reichmann H, Scheel H, Bier B, Ketelsen UP, Zabransky S.
    Ann Neurol; 1992 Jan; 31(1):107-9. PubMed ID: 1311909
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  • 15. [Leigh's syndrome].
    Sunohara N.
    Nihon Rinsho; 1990 Jul; 48(7):1568-72. PubMed ID: 2169544
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  • 16. Deficiency of pyruvate dehydrogenase complex (PDHC) in Leigh's disease fibroblasts: an abnormality in lipoamide dehydrogenase affecting PDHC activation.
    Hinman LM, Sheu KF, Baker AC, Kim YT, Blass JP.
    Neurology; 1989 Jan; 39(1):70-5. PubMed ID: 2909916
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  • 19. Leigh's disease--several nosological entities with an identical histopathological complex?
    Walter GF, Brucher JM, Martin JJ, Ceuterick C, Pilz P, Freund M.
    Neuropathol Appl Neurobiol; 1986 Jan; 12(1):95-107. PubMed ID: 3703157
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  • 20. [Leigh's syndrome and mitochondrial myopathy].
    Nakase H.
    Nihon Rinsho; 1993 Sep; 51(9):2403-8. PubMed ID: 8411720
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