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PUBMED FOR HANDHELDS

Journal Abstract Search

144 related items for PubMed ID: 8358239

  • 1. Manifesting carriers of Xp21 muscular dystrophy; lack of correlation between dystrophin expression and clinical weakness.
    Sewry CA, Sansome A, Clerk A, Sherratt TG, Hasson N, Rodillo E, Heckmatt JZ, Strong PN, Dubowitz V.
    Neuromuscul Disord; 1993 Mar; 3(2):141-8. PubMed ID: 8358239
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  • 2. Expression of dystrophin-associated glycoproteins and utrophin in carriers of Duchenne muscular dystrophy.
    Sewry CA, Matsumura K, Campbell KP, Dubowitz V.
    Neuromuscul Disord; 1994 Mar; 4(5-6):401-9. PubMed ID: 7881285
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  • 3. Heterogeneity of dystrophin expression in patients with Duchenne and Becker muscular dystrophy.
    Nicholson LV, Johnson MA, Gardner-Medwin D, Bhattacharya S, Harris JB.
    Acta Neuropathol; 1990 Mar; 80(3):239-50. PubMed ID: 2205076
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  • 4. Characterisation of dystrophin in carriers of Duchenne muscular dystrophy.
    Clerk A, Rodillo E, Heckmatt JZ, Dubowitz V, Strong PN, Sewry CA.
    J Neurol Sci; 1991 Apr; 102(2):197-205. PubMed ID: 2072119
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  • 6. Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 3. Differential diagnosis and prognosis.
    Nicholson LV, Johnson MA, Bushby KM, Gardner-Medwin D, Curtis A, Ginjaar IB, den Dunnen JT, Welch JL, Butler TJ, Bakker E.
    J Med Genet; 1993 Sep; 30(9):745-51. PubMed ID: 8411069
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  • 7. Sarcolemmal distribution of abnormal dystrophin in Xp21 carriers.
    Vainzof M, Nicholson LV, Bulman DE, Tsanaclis AM, Passos-Bueno MR, Pavanello RC, Zatz M.
    Neuromuscul Disord; 1993 Mar; 3(2):135-40. PubMed ID: 7689380
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  • 8. X inactivation and dystrophin studies in a t(X;12) female: evidence for biochemical normalization in Duchenne muscular dystrophy carriers.
    Wenger SL, Steele MW, Hoffman EP, Barmada MA, Wessel HB.
    Am J Med Genet; 1992 Aug 01; 43(6):1012-5. PubMed ID: 1415326
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  • 9. Quantitative and qualitative alterations of dystrophin are expressed in muscle cell cultures of Xp21 muscular dystrophy patients (Duchenne and Becker type).
    Mongini T, Doriguzzi C, Palmucci L, Chiadò-Piat L.
    Eur J Clin Invest; 1996 Apr 01; 26(4):322-4. PubMed ID: 8732491
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  • 10. Improved diagnosis of Becker muscular dystrophy by dystrophin testing.
    Hoffman EP, Kunkel LM, Angelini C, Clarke A, Johnson M, Harris JB.
    Neurology; 1989 Aug 01; 39(8):1011-7. PubMed ID: 2668783
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  • 11. Variability in clinical, genetic and protein abnormalities in manifesting carriers of Duchenne and Becker muscular dystrophy.
    Bushby KM, Goodship JA, Nicholson LV, Johnson MA, Haggerty ID, Gardner-Medwin D.
    Neuromuscul Disord; 1993 Jan 01; 3(1):57-64. PubMed ID: 8329890
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  • 15. Becker-like muscular dystrophy in sisters.
    Diószeghy P, Molnár M, Mechler F.
    Eur Arch Psychiatry Clin Neurosci; 1995 Jan 01; 245(6):326-30. PubMed ID: 8527470
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