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Journal Abstract Search

392 related items for PubMed ID: 7581448

  • 1. Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12.
    Lim LE, Duclos F, Broux O, Bourg N, Sunada Y, Allamand V, Meyer J, Richard I, Moomaw C, Slaughter C.
    Nat Genet; 1995 Nov; 11(3):257-65. PubMed ID: 7581448
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  • 2. 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; 49(1):19-24. PubMed ID: 11303236
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  • 3. Sarcoglycans in muscular dystrophy.
    Hack AA, Groh ME, McNally EM.
    Microsc Res Tech; 2001 Mar; 48(3-4):167-80. PubMed ID: 10679964
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  • 4. Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate.
    Duclos F, Broux O, Bourg N, Straub V, Feldman GL, Sunada Y, Lim LE, Piccolo F, Cutshall S, Gary F, Quetier F, Kaplan JC, Jackson CE, Beckmann JS, Campbell KP.
    Neuromuscul Disord; 1998 Feb; 8(1):30-8. PubMed ID: 9565988
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  • 5. [Gene analysis in patients with muscular dystrophy: alpha-sarcoglycan (adhalin) gene mutations in patients with malignant limb-girdle muscular dystrophy].
    Akaike M, Kawai H.
    Rinsho Byori; 1997 Feb; 45(2):136-40. PubMed ID: 9120997
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  • 11. Sarcoglycan complex: a muscular supporter of dystroglycan-dystrophin interplay?
    Matsumura K, Saito F, Yamada H, Hase A, Sunada Y, Shimizu T.
    Cell Mol Biol (Noisy-le-grand); 1999 Sep; 45(6):751-62. PubMed ID: 10541473
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  • 12. [Adhalin gene mutations in malignant limb-girdle muscular dystrophy and clinical features in adhalin-deficient muscular dystrophy].
    Endo T, Akaike M, Kawai H, Matsumura K, Saito S.
    Rinsho Shinkeigaku; 1996 Mar; 36(3):415-22. PubMed ID: 8741343
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  • 13. Human epsilon-sarcoglycan is highly related to alpha-sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene.
    McNally EM, Ly CT, Kunkel LM.
    FEBS Lett; 1998 Jan 23; 422(1):27-32. PubMed ID: 9475163
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  • 16. 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 23; 10(2):243-5. PubMed ID: 7663524
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  • 17. Severe limb girdle muscular dystrophy in Spanish gypsies: further evidence for a founder mutation in the gamma-sarcoglycan gene.
    Lasa A, Piccolo F, de Diego C, Jeanpierre M, Colomer J, Rodríguez MJ, Urtizberea JA, Baiget M, Kaplan J, Gallano P.
    Eur J Hum Genet; 1998 Jun 23; 6(4):396-9. PubMed ID: 9781048
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  • 20. [Significance of merosin and sarcoglycan in manifestations of certain forms of muscular dystrophy].
    Medić S, Rakocević-Stojanović V.
    Srp Arh Celok Lek; 1998 Jun 23; 126(1-2):34-9. PubMed ID: 9525081
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