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Journal Abstract Search

244 related items for PubMed ID: 2546706

  • 1. [31P-NMR spectroscopy of mitochondrial myopathies: the relation between abnormal energy metabolism and muscle biopsy findings].
    Kawai M, Itoh M, Okazawa H, Kamakura K.
    Rinsho Shinkeigaku; 1989 Feb; 29(2):167-71. PubMed ID: 2546706
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  • 2. [Mitochondrial myopathy and abnormal mitochondrial DNA].
    Takeshita K.
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):834-8. PubMed ID: 3152098
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  • 8. Myoclonic epilepsy and ragged-red fibers with cytochrome oxidase deficiency: neuropathology, biochemistry, and molecular genetics.
    Lombes A, Mendell JR, Nakase H, Barohn RJ, Bonilla E, Zeviani M, Yates AJ, Omerza J, Gales TL, Nakahara K.
    Ann Neurol; 1989 Jul; 26(1):20-33. PubMed ID: 2549843
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  • 10. Diagnosis of mitochondrial diseases: clinical and histological study of sixty patients with ragged red fibers.
    Challa S, Kanikannan MA, Murthy JM, Bhoompally VR, Surath M.
    Neurol India; 2004 Sep; 52(3):353-8. PubMed ID: 15472426
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  • 11. Deletion of mitochondrial DNA in patients with combined features of Kearns-Sayre and MELAS syndromes.
    Zupanc ML, Moraes CT, Shanske S, Langman CB, Ciafaloni E, DiMauro S.
    Ann Neurol; 1991 Jun; 29(6):680-3. PubMed ID: 1892371
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  • 12. [A case of incomplete Kearns-Sayre syndrome with a stroke like episode].
    Furuya H, Sugimura T, Yamada T, Hayashi K, Kobayashi T.
    Rinsho Shinkeigaku; 1997 Aug; 37(8):680-4. PubMed ID: 9404143
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  • 14. [A mitochondrial encephalomyopathy due to partial cytochrome c oxidase deficiency with giant evoked potentials--a case report].
    Higashi Y, Higashi S, Terao A, Yasuda T, Shirabe T.
    Rinsho Shinkeigaku; 1990 Oct; 30(10):1084-9. PubMed ID: 2177689
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  • 15. [31P-mr spectroscopy of peripheral skeletal musculature under load: demonstration of normal energy metabolites compared with metabolic muscle diseases].
    Block W, Träber F, Kuhl CK, Keller E, Lamerichs R, Karitzky J, Rink H, Schild HH.
    Rofo; 1998 Mar; 168(3):250-7. PubMed ID: 9551111
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  • 16. Peripheral neuropathy of mitochondrial myopathies.
    Mizusawa H, Ohkoshi N, Watanabe M, Kanazawa I.
    Rev Neurol (Paris); 1991 Mar; 147(6-7):501-7. PubMed ID: 1660182
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  • 17. [A case of myoclonus epilepsy associated with ragged-red fibers (MERRF) with cytochrome c oxidase deficiency].
    Taniwaki T, Yamashita Y, Ohshima Y, Habara S, Nagao H.
    Rinsho Shinkeigaku; 1988 Aug; 28(8):902-9. PubMed ID: 2853657
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  • 18. Diagnostic yield muscle biopsy in patients with clinical evidence of mitochondrial cytopathy.
    Rollins S, Prayson RA, McMahon JT, Cohen BH.
    Am J Clin Pathol; 2001 Sep; 116(3):326-30. PubMed ID: 11554158
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  • 19. Progressive cytochrome c oxidase deficiency in a case of Kearns-Sayre syndrome: morphological, immunological, and biochemical studies in muscle biopsies and autopsy tissues.
    Bresolin N, Moggio M, Bet L, Gallanti A, Prelle A, Nobile-Orazio E, Adobbati L, Ferrante C, Pellegrini G, Scarlato G.
    Ann Neurol; 1987 Jun; 21(6):564-72. PubMed ID: 3037990
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  • 20. Mitochondrial encephalomyopathies.
    Scarlato G, Moggio M, Bet L, Gallanti A, Bresolin N.
    Acta Neurol (Napoli); 1989 Oct; 11(5):322-9. PubMed ID: 2603778
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