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Journal Abstract Search

352 related items for PubMed ID: 9120997

  • 21. alpha-Sarcoglycan (adhalin) deficiency: complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutations.
    Duggan DJ, Fanin M, Pegoraro E, Angelini C, Hoffman EP.
    J Neurol Sci; 1996 Sep 01; 140(1-2):30-9. PubMed ID: 8866424
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  • 22. rAAV vector-mediated sarcogylcan gene transfer in a hamster model for limb girdle muscular dystrophy.
    Li J, Dressman D, Tsao YP, Sakamoto A, Hoffman EP, Xiao X.
    Gene Ther; 1999 Jan 01; 6(1):74-82. PubMed ID: 10341878
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  • 23. [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 01; 26(154):905-11. PubMed ID: 9658457
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  • 25. Mutations in the sarcoglycan genes in patients with myopathy.
    Duggan DJ, Gorospe JR, Fanin M, Hoffman EP, Angelini C.
    N Engl J Med; 1997 Feb 27; 336(9):618-24. PubMed ID: 9032047
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  • 28. Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency.
    Romero NB, Tomé FM, Leturcq F, el Kerch FE, Azibi K, Bachner L, Anderson RD, Roberds SL, Campbell KP, Fardeau M.
    C R Acad Sci III; 1994 Jan 27; 317(1):70-6. PubMed ID: 7987694
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  • 31. 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 27; 45(6):751-62. PubMed ID: 10541473
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  • 36. Specific assembly pathway of sarcoglycans is dependent on beta- and delta-sarcoglycan.
    Shi W, Chen Z, Schottenfeld J, Stahl RC, Kunkel LM, Chan YM.
    Muscle Nerve; 2004 Mar 27; 29(3):409-19. PubMed ID: 14981741
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  • 38. Noval mutation (Y184C) in exon 4 of the beta-sarcoglycan gene identified in a Portuguese patient. Mutations in brief no. 177. Online.
    dos Santos MR, Jorge P, Ribeiro EM, Pires MM, Guimarães A.
    Hum Mutat; 1998 Mar 27; 12(3):214-5. PubMed ID: 10660328
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