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Journal Abstract Search

392 related items for PubMed ID: 7581448

  • 21. [Muscular dystrophy due to a deficit of gamma-sarcoglycan. A report of three patients with the Delta-521t mutation].
    Eirís-Puñal J, Pintos-Martínez E, Lasa A, Gallano P, Castro-Gago M.
    Rev Neurol; ; 34(5):486-9. PubMed ID: 12040521
    [Abstract] [Full Text] [Related]

  • 22. Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12.
    Jung D, Leturcq F, Sunada Y, Duclos F, Tomé FM, Moomaw C, Merlini L, Azibi K, Chaouch M, Slaughter C, Fardeau M, Kaplan JC, Campbell KP.
    FEBS Lett; 1996 Feb 26; 381(1-2):15-20. PubMed ID: 8641426
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  • 23. Dystroglycan and muscular dystrophies related to the dystrophin-glycoprotein complex.
    Sciandra F, Bozzi M, Bianchi M, Pavoni E, Giardina B, Brancaccio A.
    Ann Ist Super Sanita; 2003 Feb 26; 39(2):173-81. PubMed ID: 14587215
    [Abstract] [Full Text] [Related]

  • 24. Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy.
    Roberds SL, Leturcq F, Allamand V, Piccolo F, Jeanpierre M, Anderson RD, Lim LE, Lee JC, Tomé FM, Romero NB.
    Cell; 1994 Aug 26; 78(4):625-33. PubMed ID: 8069911
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  • 25. [Adhalin(alpha-sarcoglycan) gene mutations in patients with malignant limb-girdle muscular dystrophy (MLGMD) (Miyoshi)].
    Endo T, Kawai H.
    Nihon Rinsho; 1997 Dec 26; 55(12):3159-64. PubMed ID: 9436428
    [Abstract] [Full Text] [Related]

  • 26. Adhalin gene mutations in patients with autosomal recessive childhood onset muscular dystrophy with adhalin deficiency.
    Kawai H, Akaike M, Endo T, Adachi K, Inui T, Mitsui T, Kashiwagi S, Fujiwara T, Okuno S, Shin S.
    J Clin Invest; 1995 Sep 26; 96(3):1202-7. PubMed ID: 7657792
    [Abstract] [Full Text] [Related]

  • 27. Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E).
    Bönnemann CG, Passos-Bueno MR, McNally EM, Vainzof M, de Sá Moreira E, Marie SK, Pavanello RC, Noguchi S, Ozawa E, Zatz M, Kunkel LM.
    Hum Mol Genet; 1996 Dec 26; 5(12):1953-61. PubMed ID: 8968749
    [Abstract] [Full Text] [Related]

  • 28. Gene transfer establishes primacy of striated vs. smooth muscle sarcoglycan complex in limb-girdle muscular dystrophy.
    Durbeej M, Sawatzki SM, Barresi R, Schmainda KM, Allamand V, Michele DE, Campbell KP.
    Proc Natl Acad Sci U S A; 2003 Jul 22; 100(15):8910-5. PubMed ID: 12851463
    [Abstract] [Full Text] [Related]

  • 29. [Gamma-sarcoglycanopathy: clinico-pathological and genetic study of 11 cases].
    García-García D, Teijeira-Bautista S, Fernández-Rodríguez JM, Flores-Calvete J, Sánchez-Espíldora P, Fernández-Couto D, Cimas-Hernando I, Teijeiro-Ferreira A, Fernández-Hojas R, Brasa-Fernández Fierros J, Martínez de Alegría A, Escribano-Arias JL, Núñez-Delgado M, Navarro-Fernández Balbuena C.
    Rev Neurol; 1998 Jun 22; 26(154):905-11. PubMed ID: 9658457
    [Abstract] [Full Text] [Related]

  • 30. Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene.
    Nigro V, de Sá Moreira E, Piluso G, Vainzof M, Belsito A, Politano L, Puca AA, Passos-Bueno MR, Zatz M.
    Nat Genet; 1996 Oct 22; 14(2):195-8. PubMed ID: 8841194
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  • 33. epsilon-Sarcoglycan, a broadly expressed homologue of the gene mutated in limb-girdle muscular dystrophy 2D.
    Ettinger AJ, Feng G, Sanes JR.
    J Biol Chem; 1997 Dec 19; 272(51):32534-8. PubMed ID: 9405466
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  • 36. Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan-deficient mice.
    Araishi K, Sasaoka T, Imamura M, Noguchi S, Hama H, Wakabayashi E, Yoshida M, Hori T, Ozawa E.
    Hum Mol Genet; 1999 Sep 19; 8(9):1589-98. PubMed ID: 10441321
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  • 38. Loss of sarcolemma nNOS in sarcoglycan-deficient muscle.
    Crosbie RH, Barresi R, Campbell KP.
    FASEB J; 2002 Nov 19; 16(13):1786-91. PubMed ID: 12409321
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