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Journal Abstract Search

140 related items for PubMed ID: 21623088

  • 1. Dysferlinopathy: spectrum of pathological changes in skeletal muscle tissue.
    Gayathri N, Alefia R, Nalini A, Yasha TC, Anita M, Santosh V, Shankar SK.
    Indian J Pathol Microbiol; 2011; 54(2):350-4. PubMed ID: 21623088
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  • 2. Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1B.
    Park YE, Hayashi YK, Goto K, Komaki H, Hayashi Y, Inuzuka T, Noguchi S, Nonaka I, Nishino I.
    Neuromuscul Disord; 2009 Jan; 19(1):29-36. PubMed ID: 19070492
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  • 3. Limb girdle muscular dystrophy type 2A in India: a study based on semi-quantitative protein analysis, with clinical and histopathological correlation.
    Pathak P, Sharma MC, Sarkar C, Jha P, Suri V, Mohd H, Singh S, Bhatia R, Gulati S.
    Neurol India; 2010 Jan; 58(4):549-54. PubMed ID: 20739790
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  • 4. Painful enlargement of the calf muscles in limb girdle muscular dystrophy type 2B (LGMD2B) with a novel compound heterozygous mutation in DYSF.
    Diers A, Carl M, Stoltenburg-Didinger G, Vorgerd M, Spuler S.
    Neuromuscul Disord; 2007 Feb; 17(2):157-62. PubMed ID: 17129727
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  • 5. Analysis of histopathologic and molecular pathologic findings in Czech LGMD2A patients.
    Hermanová M, Zapletalová E, Sedlácková J, Chrobáková T, Letocha O, Kroupová I, Zámecník J, Vondrácek P, Mazanec R, Maríková T, Vohánka S, Fajkusová L.
    Muscle Nerve; 2006 Mar; 33(3):424-32. PubMed ID: 16372320
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  • 8. Lariat branch point mutation in the dysferlin gene with mild limb-girdle muscular dystrophy.
    Sinnreich M, Therrien C, Karpati G.
    Neurology; 2006 Apr 11; 66(7):1114-6. PubMed ID: 16606933
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  • 10. Redefining dysferlinopathy phenotypes based on clinical findings and muscle imaging studies.
    Paradas C, Llauger J, Diaz-Manera J, Rojas-García R, De Luna N, Iturriaga C, Márquez C, Usón M, Hankiewicz K, Gallardo E, Illa I.
    Neurology; 2010 Jul 27; 75(4):316-23. PubMed ID: 20574037
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  • 13. [Autosomal recessive limb-girdle muscular dystrophy].
    Hernández-Caballero ME, Miranda-Duarte A, Escobar-Cedillo RE, Villegas-Castrejon H.
    Rev Neurol; 2010 Oct 16; 51(8):489-96. PubMed ID: 20925031
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  • 15. Clinical and magnetic resonance imaging features of 'diamond on quadriceps' sign in dysferlinopathy.
    Pradhan S.
    Neurol India; 2009 Oct 16; 57(2):172-5. PubMed ID: 19439848
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  • 17. SJL dystrophic mice express a significant amount of human muscle proteins following systemic delivery of human adipose-derived stromal cells without immunosuppression.
    Vieira NM, Bueno CR, Brandalise V, Moraes LV, Zucconi E, Secco M, Suzuki MF, Camargo MM, Bartolini P, Brum PC, Vainzof M, Zatz M.
    Stem Cells; 2008 Sep 16; 26(9):2391-8. PubMed ID: 18583542
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