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Journal Abstract Search

145 related items for PubMed ID: 8195819

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. [Monoclonal antibodies to dystrophin in biopsy diagnosis of Duchenne and Becker progressive muscular dystrophies].
    Lukás Z, Foretová L, Vojtísková M, Dráber P, Hájek J.
    Cesk Patol; 1994 May; 30(2):37-42. PubMed ID: 8020113
    [Abstract] [Full Text] [Related]

  • 23. Dystrophin immunohistochemistry in a symptomatic carrier of Becker muscular dystrophy.
    Haginoya K, Yamamoto K, Iinuma K, Yanagisawa T, Ichinohasama Y, Shimmoto M, Suzuki Y, Tada K.
    J Neurol; 1991 Oct; 238(7):375-8. PubMed ID: 1683669
    [Abstract] [Full Text] [Related]

  • 24. Limb-girdle syndrome: a genetic study of 22 large Brazilian families. Comparison with X-linked Duchenne and Becker dystrophies.
    Passos-Bueno MR, Vainzof M, Pavanello Rde C, Pavanello-Filho I, Lima MA, Zatz M.
    J Neurol Sci; 1991 May; 103(1):65-75. PubMed ID: 1865235
    [Abstract] [Full Text] [Related]

  • 25.
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  • 26. Dystrophin-related protein in Becker muscular dystrophy.
    Higuchi I, Niiyama T, Fukunaga H, Nakamura K, Nakagawa M, Osame M.
    Intern Med; 1994 Jun; 33(6):334-6. PubMed ID: 7919618
    [Abstract] [Full Text] [Related]

  • 27. [Separation of dystrophinopathies from the group previously classified as limb-girdle muscular dystrophies].
    Kozłowska M, Bushby K, Bisko M, Zimowski J, Badurska B.
    Neurol Neurochir Pol; 1994 Jun; 28(1 Suppl 1):115-24. PubMed ID: 8065538
    [Abstract] [Full Text] [Related]

  • 28.
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  • 29. Early onset autosomal dominant progressive muscular dystrophy presenting in childhood as a Becker phenotype--the importance of dystrophin and molecular genetic analysis.
    Miller G, Beggs AH, Towfighi J.
    Neuromuscul Disord; 1992 Jun; 2(2):121-4. PubMed ID: 1422199
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  • 30.
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  • 31. Dystrophin analysis using a panel of anti-dystrophin antibodies in Duchenne and Becker muscular dystrophy.
    Muntoni F, Mateddu A, Cianchetti C, Marrosu MG, Clerk A, Cau M, Congiu R, Cao A, Melis MA.
    J Neurol Neurosurg Psychiatry; 1993 Jan; 56(1):26-31. PubMed ID: 8429320
    [Abstract] [Full Text] [Related]

  • 32.
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  • 33. Is the maintainance of the C-terminus domain of dystrophin enough to ensure a milder Becker muscular dystrophy phenotype?
    Vainzof M, Takata RI, Passos-Bueno MR, Pavanello RC, Zatz M.
    Hum Mol Genet; 1993 Jan; 2(1):39-42. PubMed ID: 8490621
    [Abstract] [Full Text] [Related]

  • 34. Asymptomatic Becker muscular dystrophy: histological changes in biopsied muscles.
    Tachi N, Watanabe Y, Ohya K, Chiba S.
    Acta Paediatr Jpn; 1993 Oct; 35(5):409-11. PubMed ID: 8256625
    [Abstract] [Full Text] [Related]

  • 35. [Application of combined DNA and dystrophin protein analysis in the diagnosis of Duchenne's and Becker's muscular dystrophy in 102 Dutch patients].
    Ginjaar HB, Bakker E, Busch HF, Moorman AF, de Visser M, van Ommen JB.
    Ned Tijdschr Geneeskd; 1993 Jan 09; 137(2):68-75. PubMed ID: 8421530
    [Abstract] [Full Text] [Related]

  • 36. Preservation of the C-terminus of dystrophin molecule in the skeletal muscle from Becker muscular dystrophy.
    Arahata K, Beggs AH, Honda H, Ito S, Ishiura S, Tsukahara T, Ishiguro T, Eguchi C, Orimo S, Arikawa E.
    J Neurol Sci; 1991 Feb 09; 101(2):148-56. PubMed ID: 2033400
    [Abstract] [Full Text] [Related]

  • 37. Is dystrophin labelling always discontinuous in Becker muscular dystrophy?
    Slater CR, Nicholson LV.
    J Neurol Sci; 1991 Feb 09; 101(2):187-92. PubMed ID: 2033404
    [Abstract] [Full Text] [Related]

  • 38.
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  • 39. Epidemiology of progressive muscular dystrophy in Okinawa, Japan. Classification with molecular biological techniques.
    Nakagawa M, Nakahara K, Yoshidome H, Suehara M, Higuchi I, Fujiyama J, Nakamura A, Kubota R, Takenaga S, Arahata K.
    Neuroepidemiology; 1991 Feb 09; 10(4):185-91. PubMed ID: 1745328
    [Abstract] [Full Text] [Related]

  • 40.
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