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Journal Abstract Search

169 related items for PubMed ID: 2547913

  • 1. 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; 236(4):218-22. PubMed ID: 2547913
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  • 2. [Delayed manifestation of mitochondrial myopathy--complex I and IV deficiency of the mitochondrial respiratory chain with progressive paresis].
    Beyenburg S, von Wersebe O, Zierz S.
    Nervenarzt; 1991 Aug; 62(8):506-11. PubMed ID: 1658669
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  • 3. [Kearns-Sayre syndrome: mitochondrial encephalomyopathy caused by deficiency of the respiratory chain].
    Desnuelle C, Pellissier JF, Serratrice G, Pouget J, Turnbull DM.
    Rev Neurol (Paris); 1989 Aug; 145(12):842-50. PubMed ID: 2559448
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  • 4. Familial mitochondrial myopathy associated with peripheral neuropathy: partial deficiencies of complex I and complex IV.
    Mizusawa H, Watanabe M, Kanazawa I, Nakanishi T, Kobayashi M, Tanaka M, Suzuki H, Nishikimi M, Ozawa T.
    J Neurol Sci; 1988 Sep; 86(2-3):171-84. PubMed ID: 2851645
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  • 12. Partial cytochrome oxidase (aa3) deficiency in chronic progressive external ophthalmoplegia. Histochemical and biochemical studies.
    Byrne E, Dennett X, Trounce I, Henderson R.
    J Neurol Sci; 1985 Dec; 71(2-3):257-71. PubMed ID: 2418159
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  • 13. Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome and NADH-CoQ reductase deficiency.
    Kobayashi M, Morishita H, Sugiyama N, Yokochi K, Nakano M, Wada Y, Hotta Y, Terauchi A, Nonaka I.
    J Inherit Metab Dis; 1986 Dec; 9(3):301-4. PubMed ID: 3099078
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  • 14. [A case of mitochondrial encephalomyopathy with cardiomyopathy due to decreased complex I and IV activities].
    Kajiyama M, Kawamura I, Fujita A, Hamamoto K, Nishi Y, Kitano A, Matsuda I, Ohtani Y, Miike T.
    No To Hattatsu; 1989 Jul; 21(4):369-73. PubMed ID: 2551357
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  • 15. [Muscle pathology in mitochondrial myopathy].
    Nonaka I.
    No To Hattatsu; 1987 Mar; 19(2):110-7. PubMed ID: 3030377
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  • 16. Impaired mitochondrial beta-oxidation in a patient with an abnormality of the respiratory chain. Studies in skeletal muscle mitochondria.
    Watmough NJ, Bindoff LA, Birch-Machin MA, Jackson S, Bartlett K, Ragan CI, Poulton J, Gardiner RM, Sherratt HS, Turnbull DM.
    J Clin Invest; 1990 Jan; 85(1):177-84. PubMed ID: 2153151
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  • 17. Partial cytochrome oxidase deficiency without subsarcolemmal accumulation of mitochondria in chronic progressive external ophthalmoplegia.
    Turnbull DM, Johnson MA, Dick DJ, Cartlidge NE, Sherratt HS.
    J Neurol Sci; 1985 Aug; 70(1):93-100. PubMed ID: 2995595
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  • 18. [Neurological approach to mitochondrial abnormalities].
    Yokochi K.
    No To Hattatsu; 1987 Mar; 19(2):118-24. PubMed ID: 3030378
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  • 19. Focal cytochrome c oxidase deficiency in various neuromuscular diseases.
    Yamamoto M, Koga Y, Ohtaki E, Nonaka I.
    J Neurol Sci; 1989 Jun; 91(1-2):207-13. PubMed ID: 2545831
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  • 20. Immunocytological and histochemical correlation in Kearns-Sayre syndrome with mtDNA deletion and partial cytochrome c oxidase deficiency in skeletal muscle.
    Romero NB, Lestienne P, Marsac C, Paturneau-Jouas M, Nelson I, François D, Eymard B, Fardeau M.
    J Neurol Sci; 1989 Nov; 93(2-3):297-309. PubMed ID: 2556504
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