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Journal Abstract Search

232 related items for PubMed ID: 2156958

  • 1. Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes.
    Gerbitz KD, Obermaier-Kusser B, Zierz S, Pongratz D, Müller-Höcker J, Lestienne P.
    J Neurol; 1990 Feb; 237(1):5-10. PubMed ID: 2156958
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  • 3. Segmental cytochrome c-oxidase deficiency in CPEO: teased muscle fiber analysis.
    Matsuoka T, Goto Y, Hasegawa H, Nonaka I.
    Muscle Nerve; 1992 Feb; 15(2):209-13. PubMed ID: 1312676
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  • 8. Are duplications of mitochondrial DNA characteristic of Kearns-Sayre syndrome?
    Poulton J, Morten KJ, Weber K, Brown GK, Bindoff L.
    Hum Mol Genet; 1994 Jun; 3(6):947-51. PubMed ID: 7951243
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  • 10. Duplications of mitochondrial DNA in Kearns-Sayre syndrome.
    Poulton J, Morten KJ, Marchington D, Weber K, Brown GK, Rötig A, Bindoff L.
    Muscle Nerve Suppl; 1995 Jun; 3():S154-8. PubMed ID: 7603518
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  • 15. Mitochondrial DNA defects in Brazilian patients with chronic progressive external ophthalmoplegia.
    Kiyomoto BH, Tengan CH, Moraes CT, Oliveira AS, Gabbai AA.
    J Neurol Sci; 1997 Nov 25; 152(2):160-5. PubMed ID: 9415537
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  • 16. Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres.
    Oldfors A, Larsson NG, Holme E, Tulinius M, Kadenbach B, Droste M.
    J Neurol Sci; 1992 Jul 25; 110(1-2):169-77. PubMed ID: 1324295
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  • 17. Localization of mitochondrial DNA in normal and pathological muscle using immunological probes: a new approach to the study of mitochondrial myopathies.
    Andreetta F, Tritschler HJ, Schon EA, DiMauro S, Bonilla E.
    J Neurol Sci; 1991 Sep 25; 105(1):88-92. PubMed ID: 1665507
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  • 18. Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome.
    Mita S, Schmidt B, Schon EA, DiMauro S, Bonilla E.
    Proc Natl Acad Sci U S A; 1989 Dec 25; 86(23):9509-13. PubMed ID: 2556715
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  • 19. The clinical, myopathological, and genetic analysis of 155 Chinese mitochondrial ophthalmoplegia patients with mitochondrial DNA single large deletions.
    Zhao Y, Hou Y, Zhao X, Liufu T, Yu M, Zhang W, Xie Z, Zhang VW, Yuan Y, Wang Z.
    Mol Genet Genomic Med; 2024 Jan 25; 12(1):e2328. PubMed ID: 38018320
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  • 20. Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesis.
    Nakase H, Moraes CT, Rizzuto R, Lombes A, DiMauro S, Schon EA.
    Am J Hum Genet; 1990 Mar 25; 46(3):418-27. PubMed ID: 1689952
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