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Journal Abstract Search

348 related items for PubMed ID: 3323392

  • 21. [Congenital nemaline myopathy with mitochondrial abnormalities. An adult case report].
    Oya Y, Segawa M, Ogawa M, Goto Y, Nonaka I, Kawai M.
    Rinsho Shinkeigaku; 2000 May; 40(5):452-8. PubMed ID: 11002727
    [Abstract] [Full Text] [Related]

  • 22. Mitochondrial myopathies.
    DiMauro S, Bonilla E, Zeviani M, Nakagawa M, DeVivo DC.
    Ann Neurol; 1985 Jun; 17(6):521-38. PubMed ID: 3927817
    [Abstract] [Full Text] [Related]

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  • 25. Congenital myopathy with focal loss of cross striations: a case report with morphologic and immunohistochemical study.
    Yun Y, Bergmann M, Klein H, Sternowsky HJ.
    Gen Diagn Pathol; 1995 Oct; 141(2):155-60. PubMed ID: 8548596
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  • 27. Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene.
    Jungbluth H, Zhou H, Hartley L, Halliger-Keller B, Messina S, Longman C, Brockington M, Robb SA, Straub V, Voit T, Swash M, Ferreiro A, Bydder G, Sewry CA, Müller C, Muntoni F.
    Neurology; 2005 Dec 27; 65(12):1930-5. PubMed ID: 16380615
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  • 29. Congenital myopathies.
    Bodensteiner J.
    Neurol Clin; 1988 Aug 27; 6(3):499-518. PubMed ID: 3065597
    [Abstract] [Full Text] [Related]

  • 30. [A 34-year-old woman with delayed motor milestones, high arched palate, and proximal muscle weakness].
    Yamamoto T, Kitada T, Hirasawa E, Mori H, Mizuno Y.
    No To Shinkei; 1996 Jul 27; 48(7):677-84. PubMed ID: 8753005
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  • 31. [Nemaline myopathy (clinico-morphologic study)].
    Il'ina NA, Sokolina NA, Aver'ianov IuN, Korolev VV, Golovakina AN.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1978 Jul 27; 78(10):1447-50. PubMed ID: 716716
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  • 32. The myopathology of floppy and hypotonic infants in Singapore.
    Premasiri MK, Lee YS.
    Pathology; 2003 Oct 27; 35(5):409-13. PubMed ID: 14555385
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  • 33. 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 Oct 27; 21(5):220-31. PubMed ID: 12365725
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  • 34. [An unusual myopathy: the so-called congenital fiber-type disproportion].
    Lössner J, Ziegan J, Oertel G.
    Z Gesamte Inn Med; 1979 Nov 15; 34(22):685-7. PubMed ID: 549303
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  • 36. Multicore disease. A recently recognized congenital myopathy associated with multifocal degeneration of muscle fibers.
    Engel AG, Gomez MR, Groover RV.
    Mayo Clin Proc; 1971 Oct 15; 46(10):666-81. PubMed ID: 5115748
    [No Abstract] [Full Text] [Related]

  • 37. Metabolic myopathies.
    Gullotta F.
    Pathol Res Pract; 1985 Jul 15; 180(1):10-8. PubMed ID: 3862080
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  • 39. [Multicore myopathy--a case of congenital non-progressive myopathy associated with "multicore" degeneration of muscle fibers].
    Tanimura R, Suzuki Y, Segawa M, Fukuyama Y.
    Rinsho Shinkeigaku; 1974 Jul 01; 14(7):613-22. PubMed ID: 4473307
    [No Abstract] [Full Text] [Related]

  • 40. CONGENITAL NONPROGRESSIVE MYOPATHY. CENTRAL CORE DISEASE AND NEMALINE MYOPATHY IN ONE FAMILY.
    AFIFI AK, SMITH JW, ZELLWEGER H.
    Neurology; 1965 Apr 01; 15():371-81. PubMed ID: 14280602
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