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Journal Abstract Search

294 related items for PubMed ID: 1842672

  • 21. 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; 80(3):239-50. PubMed ID: 2205076
    [Abstract] [Full Text] [Related]

  • 22. A case of Becker muscular dystrophy resulting from the skipping of four contiguous exons (71-74) of the dystrophin gene during mRNA maturation.
    Patria SY, Alimsardjono H, Nishio H, Takeshima Y, Nakamura H, Matsuo M.
    Proc Assoc Am Physicians; 1996 Jul; 108(4):308-14. PubMed ID: 8863344
    [Abstract] [Full Text] [Related]

  • 23. Is the carboxyl-terminus of dystrophin required for membrane association? A novel, severe case of Duchenne muscular dystrophy.
    Hoffman EP, Garcia CA, Chamberlain JS, Angelini C, Lupski JR, Fenwick R.
    Ann Neurol; 1991 Oct; 30(4):605-10. PubMed ID: 1789686
    [Abstract] [Full Text] [Related]

  • 24. 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
    [Abstract] [Full Text] [Related]

  • 25. Is dystrophin always altered in Becker muscular dystrophy patients?
    Vainzof M, Passos-Bueno MR, Pavanello RC, Zatz M.
    J Neurol Sci; 1995 Jul 01; 131(1):99-104. PubMed ID: 7561956
    [Abstract] [Full Text] [Related]

  • 26. 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 Jul 01; 2(2):121-4. PubMed ID: 1422199
    [Abstract] [Full Text] [Related]

  • 27. Dystrophinopathies in females.
    Hausmanowa-Petrusewicz I, Fidziańska A, Niebrój-Dobosz I, Dorobek M, Bojakowski J.
    Folia Neuropathol; 2000 Jul 01; 38(1):7-12. PubMed ID: 11057028
    [Abstract] [Full Text] [Related]

  • 28. Systematic use of dystrophin testing in muscle biopsies: results in 201 cases.
    Doriguzzi C, Palmucci L, Mongini T, Chiadò-Piat L, Maniscalco M, Restagno G.
    Eur J Clin Invest; 1997 Apr 01; 27(4):352-8. PubMed ID: 9134386
    [Abstract] [Full Text] [Related]

  • 29. [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 Apr 01; 28(1 Suppl 1):115-24. PubMed ID: 8065538
    [Abstract] [Full Text] [Related]

  • 30. Distinction of Becker from limb-girdle muscular dystrophy by means of dystrophin cDNA probes.
    Norman A, Thomas N, Coakley J, Harper P.
    Lancet; 1989 Mar 04; 1(8636):466-8. PubMed ID: 2563842
    [Abstract] [Full Text] [Related]

  • 31. [Dystrophin and dystrophin-associated proteins. Their evaluation at the neuromuscular pathology laboratory].
    Navarro C.
    Rev Neurol; 1989 Mar 04; 28(2):154-8. PubMed ID: 10101784
    [Abstract] [Full Text] [Related]

  • 32. Carrier detection of Duchenne and Becker muscular dystrophy using muscle dystrophin immunohistochemistry.
    Oliveira AS, Gabbai AA, Schmidt B, Kiyomoto BH, Lima JG, Minetti C, Bonilla E.
    Arq Neuropsiquiatr; 1992 Dec 04; 50(4):478-85. PubMed ID: 1309152
    [Abstract] [Full Text] [Related]

  • 33. PCR and immunoblot analyses of dystrophin in Becker muscular dystrophy.
    Uchino M, Miike T, Iwashita H, Uyama E, Yoshioka K, Sugino S, Ando M.
    J Neurol Sci; 1994 Jul 04; 124(2):225-9. PubMed ID: 7964876
    [Abstract] [Full Text] [Related]

  • 34. Absence of dystrophin in two patients with Becker type Xp21 muscular dystrophy.
    Mongini T, Palmucci L, Doriguzzi C, Chiadoò-Piat L, Restagno G.
    Neurosci Lett; 1992 Nov 23; 147(1):37-40. PubMed ID: 1480320
    [Abstract] [Full Text] [Related]

  • 35. [Association between dystrophin and neuronal nitric oxide synthase in muscles of progressive muscular dystrophy].
    Wang S, Shen D.
    Zhonghua Yi Xue Za Zhi; 2002 Feb 10; 82(3):155-7. PubMed ID: 11953148
    [Abstract] [Full Text] [Related]

  • 36. Immunohistochemical alterations of dystrophin in congenital muscular dystrophy.
    Werneck LC, Bonilla E.
    Arq Neuropsiquiatr; 1995 Sep 10; 53(3-A):416-23. PubMed ID: 8540815
    [Abstract] [Full Text] [Related]

  • 37. Becker muscular dystrophy: demonstration of the carrier status of a female by immunoblotting and immunostaining.
    Chevron MP, Tuffery S, Echenne B, Demaille J, Claustres M.
    Neuromuscul Disord; 1992 Sep 10; 2(1):47-50. PubMed ID: 1525558
    [Abstract] [Full Text] [Related]

  • 38. Very small dystrophin molecule in a family with a mild form of Becker dystrophy.
    Morandi L, Mora M, Bernasconi P, Mantegazza R, Gebbia M, Balestrini MR, Cornelio F.
    Neuromuscul Disord; 1993 Jan 10; 3(1):65-70. PubMed ID: 8329891
    [Abstract] [Full Text] [Related]

  • 39. Recent advances in diagnosis of the childhood muscular dystrophies.
    Jones KJ, North KN.
    J Paediatr Child Health; 1997 Jun 10; 33(3):195-201. PubMed ID: 9259292
    [Abstract] [Full Text] [Related]

  • 40. Cardiac dystrophin abnormalities in Becker muscular dystrophy assessed by endomyocardial biopsy.
    Maeda M, Nakao S, Miyazato H, Setoguchi M, Arima S, Higuchi I, Osame M, Taira A, Nomoto K, Toda H.
    Am Heart J; 1995 Apr 10; 129(4):702-7. PubMed ID: 7900621
    [Abstract] [Full Text] [Related]

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