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Journal Abstract Search

657 related items for PubMed ID: 9851444

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  • 3. Screening of male patients with autosomal recessive Duchenne dystrophy through dystrophin and DNA studies.
    Vainzof M, Pavanello RC, Pavanello-Filho I, Rapaport D, Passos-Bueno MR, Zubrzycka-Gaarn EE, Bulman DE, Zatz M.
    Am J Med Genet; 1991 Apr 01; 39(1):38-41. PubMed ID: 1867262
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  • 4. Genomic organization of the MTM1 gene implicated in X-linked myotubular myopathy.
    Laporte J, Guiraud-Chaumeil C, Tanner SM, Blondeau F, Hu LJ, Vicaire S, Liechti-Gallati S, Mandel JL.
    Eur J Hum Genet; 1998 Apr 01; 6(4):325-30. PubMed ID: 9781038
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  • 7. Normal dystrophin in McLeod myopathy.
    Danek A, Witt TN, Stockmann HB, Weiss BJ, Schotland DL, Fischbeck KH.
    Ann Neurol; 1990 Nov 01; 28(5):720-2. PubMed ID: 2260862
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  • 8. Dystrophin immunocytochemistry in muscle culture: detection of a carrier of Duchenne muscular dystrophy.
    Miranda AF, Francke U, Bonilla E, Martucci G, Schmidt B, Salviati G, Rubin M.
    Am J Med Genet; 1989 Feb 01; 32(2):268-73. PubMed ID: 2648829
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  • 9. Duchenne muscular dystrophy in a girl identified by dystrophin deficiency.
    Maytal J, Shanske AL, Fox JE, Lipper S, Eviatar L.
    Neuropediatrics; 1991 Aug 01; 22(3):163-5. PubMed ID: 1944823
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  • 11. A gene mutated in X-linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast.
    Laporte J, Hu LJ, Kretz C, Mandel JL, Kioschis P, Coy JF, Klauck SM, Poustka A, Dahl N.
    Nat Genet; 1996 Jun 01; 13(2):175-82. PubMed ID: 8640223
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  • 14. X-linked myotubular myopathy: report of a case with novel mutation.
    Hortobágyi T, Szabó H, Kovács KS, Bódi I, Bereg E, Katona M, Biancalana V, Túri S, Sztriha L.
    J Child Neurol; 2007 Apr 01; 22(4):447-51. PubMed ID: 17621527
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  • 16. Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin.
    Matsumura K, Tomé FM, Ionasescu V, Ervasti JM, Anderson RD, Romero NB, Simon D, Récan D, Kaplan JC, Fardeau M.
    J Clin Invest; 1993 Aug 01; 92(2):866-71. PubMed ID: 8349821
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  • 17. Utility of dystrophin and utrophin staining in childhood muscular dystrophy.
    Sundaram C, Vydehi B, Meena K, Murthy J.
    Indian J Pathol Microbiol; 2004 Jul 01; 47(3):367-9. PubMed ID: 16295426
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  • 18. Quadriceps myopathy: forme fruste of Becker muscular dystrophy.
    Sunohara N, Arahata K, Hoffman EP, Yamada H, Nishimiya J, Arikawa E, Kaido M, Nonaka I, Sugita H.
    Ann Neurol; 1990 Nov 01; 28(5):634-9. PubMed ID: 2260849
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  • 19. Nitric oxide synthase I (NOS-I) is deficient in the sarcolemma of striated muscle fibers in patients with Duchenne muscular dystrophy, suggesting an association with dystrophin.
    Grozdanovic Z, Gosztonyi G, Gossrau R.
    Acta Histochem; 1996 Jan 01; 98(1):61-9. PubMed ID: 9054190
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  • 20. X-linked dystrophies: from gene localization to gene therapy.
    Chamberlain JS.
    Curr Opin Neurol Neurosurg; 1992 Oct 01; 5(5):610-4. PubMed ID: 1392134
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