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Journal Abstract Search

147 related items for PubMed ID: 8140891

  • 1. Reducing body myopathy and desmin storage in skeletal muscle: morphological and biochemical findings.
    Bertini E, Salviati G, Apollo F, Ricci E, Servidei S, Broccolini A, Papacci M, Tonali P.
    Acta Neuropathol; 1994; 87(1):106-12. PubMed ID: 8140891
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  • 5. Hereditary distal myopathy with granulo-filamentous cytoplasmic inclusions containing desmin, dystrophin and vimentin.
    Helliwell TR, Green AR, Green A, Edwards RH.
    J Neurol Sci; 1994 Jul; 124(2):174-87. PubMed ID: 7964869
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  • 6. Desmin and actin associated with cytoplasmic bodies in skeletal muscle fibers: immunocytochemical and fine structural studies, with a note on unusual 18- to 20-nm filaments.
    Schröder JM, Sommer C, Schmidt B.
    Acta Neuropathol; 1990 Jul; 80(4):406-14. PubMed ID: 2173329
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  • 11. Expression of caveolar components in primary desminopathy.
    Shinde A, Nakano S, Sugawara M, Toyoshima I, Ito H, Tanaka K, Kusaka H.
    Neuromuscul Disord; 2008 Mar; 18(3):215-9. PubMed ID: 18343114
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  • 14. The cytoplasmic bodies in a congenital myopathy can be stained with antibodies to desmin, the muscle-specific intermediate filament protein.
    Osborn M, Goebel HH.
    Acta Neuropathol; 1983 Mar; 62(1-2):149-52. PubMed ID: 6318501
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  • 15. Myofibrillar (desmin-related) myopathy: clinico-pathological spectrum in 3 cases and review of the literature.
    Wanschit J, Nakano S, Goudeau B, Ströbel T, Rinner W, Wimmer G, Resch H, Jaksch M, Akiguchi I, Vicart P, Budka H.
    Clin Neuropathol; 2002 Mar; 21(5):220-31. PubMed ID: 12365725
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  • 16. New observations in reducing body myopathy.
    Carpenter S, Karpati G, Holland P.
    Neurology; 1985 Jun; 35(6):818-27. PubMed ID: 4000482
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  • 18. [Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material without mutation of the alphabeta-crystallin gene].
    Pou Serradell A, Lloreta Trull J, Corominas Torres J, Guicheney P.
    Neurologia; 2001 May; 16(5):195-203. PubMed ID: 11412718
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