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Journal Abstract Search

131 related items for PubMed ID: 3683878

  • 1. 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; 37(12):1867-9. PubMed ID: 3683878
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  • 2. [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
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  • 3. Mitochondrial cytopathy.
    Ito T, Hattori K, Tanaka M, Sugiyama S, Ozawa T.
    Jpn Circ J; 1990 Sep; 54(9):1214-20. PubMed ID: 2266580
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  • 8. Biochemical studies in mitochondrial encephalomyopathy.
    Goda S, Ishimoto S, Goto I, Kuroiwa Y, Koike K, Koike M, Nakagawa M, Reichmann H, DiMauro S.
    J Neurol Neurosurg Psychiatry; 1987 Oct; 50(10):1348-52. PubMed ID: 3681314
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  • 10. A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).
    Goto Y, Nonaka I, Horai S.
    Biochim Biophys Acta; 1991 Oct 21; 1097(3):238-40. PubMed ID: 1932147
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  • 11. [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 21; 27(8):969-75. PubMed ID: 3690923
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  • 12. [Mitochondrial encephalomyopathy, lactic acidosis and features of cerebrovascular disorders].
    Mesa T, Hoppe A, Soza M.
    Rev Chil Pediatr; 1990 Aug 21; 61(3):143-8. PubMed ID: 2077586
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  • 13. Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS): adolescent onset with severe cerebral edema.
    Danks RA, Dorevitch M, Cummins JT, Byrne E.
    Aust N Z J Med; 1988 Feb 21; 18(1):69-72. PubMed ID: 3395302
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