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Journal Abstract Search

168 related items for PubMed ID: 3121229

  • 1. [Familial cases of mitochondrial cytopathy].
    Ishitsu T, Matsuda I, Kitano A, Shimoji A, Kimura H.
    Rinsho Shinkeigaku; 1987 Aug; 27(8):983-9. PubMed ID: 3121229
    [No Abstract] [Full Text] [Related]

  • 2. Mitochondrial cytopathy.
    Ito T, Hattori K, Tanaka M, Sugiyama S, Ozawa T.
    Jpn Circ J; 1990 Sep; 54(9):1214-20. PubMed ID: 2266580
    [No Abstract] [Full Text] [Related]

  • 3. [Mitochondrial abnormalities and diseases].
    Goto Y, Sugita H.
    Nihon Naika Gakkai Zasshi; 1991 May 10; 80(5):775-80. PubMed ID: 1651974
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  • 7. [Mitochondrial encephalomyopathy].
    Scarlato G, Bresolin N, Moggio M, Bet L, Meola G.
    Recenti Prog Med; 1989 Dec 10; 80(12):665-72. PubMed ID: 2560839
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  • 9. [Mitochondrial encephalomyopathy].
    Ozawa T, Tanaka M.
    Tanpakushitsu Kakusan Koso; 1990 May 10; 35(7 Suppl):1236-45. PubMed ID: 2162552
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  • 10. 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 10; 29(6):680-3. PubMed ID: 1892371
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  • 14. [A case of mitochondrial encephalomyopathy--Mitochondrial myopathy, encephalopathy, lactic acidosis and strokelike episodes (MELAS)].
    Ihara Y, Namba R, Demiya M, Matsumoto T, Shirabe T.
    Rinsho Shinkeigaku; 1987 Aug 10; 27(8):969-75. PubMed ID: 3690923
    [No Abstract] [Full Text] [Related]

  • 15. Heterogeneous phenotypes of mitochondrial encephalomyopathy in a single kindred.
    Ishitsu T, Miike T, Kitano A, Haraguchi Y, Ohtani Y, Matsuda I, Shimoji A, Kimura H.
    Neurology; 1987 Dec 10; 37(12):1867-9. PubMed ID: 3683878
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