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Journal Abstract Search


202 related items for PubMed ID: 7898714

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  • 7. Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophy.
    Matsumura K, Nonaka I, Campbell KP.
    Lancet; 1993 Feb 27; 341(8844):521-2. PubMed ID: 8094772
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  • 10. Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle.
    Matsumura K, Ervasti JM, Ohlendieck K, Kahl SD, Campbell KP.
    Nature; 1992 Dec 10; 360(6404):588-91. PubMed ID: 1461282
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  • 12. Deficiency of the 50 kDa dystrophin-associated-glycoprotein (adhalin) in an Indian autosomal recessive limb girdle muscular dystrophy patient : immunochemical analysis and clinical aspects.
    Handa V, Mital A, Gupta M, Goyle S.
    Neurol India; 2001 Mar 10; 49(1):19-24. PubMed ID: 11303236
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  • 13. Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin.
    Higuchi I, Yamada H, Fukunaga H, Iwaki H, Okubo R, Nakagawa M, Osame M, Roberds SL, Shimizu T, Campbell KP.
    J Clin Invest; 1994 Aug 10; 94(2):601-6. PubMed ID: 8040315
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  • 14. Increased expression of dystrophin, beta-dystroglycan and adhalin in denervated rat muscles.
    Biral D, Senter L, Salviati G.
    J Muscle Res Cell Motil; 1996 Oct 10; 17(5):523-32. PubMed ID: 8906620
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  • 15. Primary adhalin deficiency as a cause of muscular dystrophy in patients with normal dystrophin.
    Ljunggren A, Duggan D, McNally E, Boylan KB, Gama CH, Kunkel LM, Hoffman EP.
    Ann Neurol; 1995 Sep 10; 38(3):367-72. PubMed ID: 7668821
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  • 17. Dystrophin-associated protein abnormalities in dystrophin-deficient muscle fibers from symptomatic and asymptomatic Duchenne/Becker muscular dystrophy carriers.
    Di Blasi C, Morandi L, Barresi R, Blasevich F, Cornelio F, Mora M.
    Acta Neuropathol; 1996 Oct 10; 92(4):369-77. PubMed ID: 8891069
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  • 20. Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity.
    Piccolo F, Roberds SL, Jeanpierre M, Leturcq F, Azibi K, Beldjord C, Carrié A, Récan D, Chaouch M, Reghis A.
    Nat Genet; 1995 Jun 10; 10(2):243-5. PubMed ID: 7663524
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