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Journal Abstract Search

102 related items for PubMed ID: 1653096

  • 1. [Nemaline myopathy--a case report].
    Chen CW, Chi CS, Mak SC, Chu HY, Ho L.
    Zhonghua Yi Xue Za Zhi (Taipei); 1991 Jul; 48(1):66-70. PubMed ID: 1653096
    [Abstract] [Full Text] [Related]

  • 2. [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; 48(7):677-84. PubMed ID: 8753005
    [Abstract] [Full Text] [Related]

  • 3. [Nemaline myopathy. General review apropos of 3 cases].
    Pagès M, Ramos J, Pagès AM, Echenne B.
    Ann Pathol; 1987 Jul; 7(3):216-22. PubMed ID: 3325069
    [Abstract] [Full Text] [Related]

  • 4. [Two adult cases of nemaline myopathy presenting different clinical symptoms and CT findings].
    Tajima Y, Yoshida A, Ura S.
    No To Shinkei; 2001 Jul; 53(7):653-8. PubMed ID: 11517491
    [Abstract] [Full Text] [Related]

  • 5. Mental retardation in congenital nonprogressive myopathy with uniform type 1 fibers.
    Jong YJ, Huang SC, Liu GC, Chiang CH.
    Brain Dev; 1991 Nov; 13(6):444-6. PubMed ID: 1810161
    [Abstract] [Full Text] [Related]

  • 6. [An adult case of congenital myopathy--coexistence of nemaline rods and core-like structures].
    Eto K, Watanabe T, Ida M, Kojima S, Takagi A, Narui K.
    Rinsho Shinkeigaku; 1994 Jan; 34(1):43-7. PubMed ID: 8156709
    [Abstract] [Full Text] [Related]

  • 7. [An adulthood progressive case of congenital nemaline myopathy showing rimmed vacuoles in muscle biopsy and diffuse neurogenic changes on electromyography].
    Ikezoe K, Murai H, Kawajiri M, Ohyagi Y, Kira J.
    Rinsho Shinkeigaku; 2004 Jul; 44(7):450-3. PubMed ID: 15384708
    [Abstract] [Full Text] [Related]

  • 8. [Nemaline myopathy with type 2 fiber predominance; a case report].
    Sunaga Y, Fujinaga T, Tamura H.
    No To Hattatsu; 1991 Jul; 23(4):380-3. PubMed ID: 1651744
    [Abstract] [Full Text] [Related]

  • 9. A case of nemaline myopathy with ophthalmoplegia and mitochondrial abnormalities.
    Fukunaga H, Osame M, Igata A.
    J Neurol Sci; 1980 May; 46(2):169-77. PubMed ID: 6247453
    [Abstract] [Full Text] [Related]

  • 10. [A 22-year-old man with long-standing weakness and atrophy predominantly in the lower extremities].
    Mori H, Sato K, Hirasawa E, Kondo T, Mizuno Y.
    No To Shinkei; 1996 Aug; 48(8):763-71. PubMed ID: 8797213
    [Abstract] [Full Text] [Related]

  • 11. [Reducing body myopathy--a case report].
    Kobayashi Y, Nihei K, Kuwajima K, Nonaka I.
    Rinsho Shinkeigaku; 1992 Jan; 32(1):62-7. PubMed ID: 1321016
    [Abstract] [Full Text] [Related]

  • 12. [An electrophoretic study of the muscle proteins in nemaline myopathy: a new method using type-defined freeze-dried sections].
    Tanaka K, Toyoshima I, Fukuhara N, Miyatake T.
    No To Shinkei; 1984 Jan; 36(1):57-63. PubMed ID: 6732976
    [Abstract] [Full Text] [Related]

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  • 14. [A patient of late-onset nemaline myopathy with mononuclear cell infiltration].
    Miura H, Kannari K, Kashiwamura H, Nonaka I.
    Rinsho Shinkeigaku; 1994 Oct; 34(10):1061-3. PubMed ID: 7834955
    [Abstract] [Full Text] [Related]

  • 15. Nemaline myopathy.
    Greenwood SM, Viozzi FJ.
    Arch Pathol Lab Med; 1978 Apr; 102(4):196-200. PubMed ID: 580714
    [Abstract] [Full Text] [Related]

  • 16. [Nemaline myopathy: report of a case with a histochemical and electron microscopy study].
    Werneck LC, Silvado CE, Jamur MC, Yacubian EM, Salum PN.
    Arq Neuropsiquiatr; 1983 Jun; 41(2):199-207. PubMed ID: 6639404
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  • 18. Congenital myopathy without specific features (minimal change myopathy).
    Nonaka I, Nakamura Y, Tojo M, Sugita H, Ishikawa T, Awaya A, Sugiyama N.
    Neuropediatrics; 1983 Nov; 14(4):237-41. PubMed ID: 6657012
    [Abstract] [Full Text] [Related]

  • 19. Fatal neonatal nemaline myopathy.
    Matsuo T, Tashiro T, Ikeda T, Tsujihata M, Shimomura C.
    Acta Pathol Jpn; 1982 Sep; 32(5):907-16. PubMed ID: 6182741
    [Abstract] [Full Text] [Related]

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