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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

372 related items for PubMed ID: 9505924

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  • 4. Abnormalities in alpha-, beta- and gamma-sarcoglycan in patients with limb-girdle muscular dystrophy.
    Sewry CA, Taylor J, Anderson LV, Ozawa E, Pogue R, Piccolo F, Bushby K, Dubowitz V, Muntoni F.
    Neuromuscul Disord; 1996 Dec; 6(6):467-74. PubMed ID: 9027857
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  • 5. Autosomal recessive muscular dystrophy and mutations of the sarcoglycan complex.
    Duggan DJ, Hoffman EP.
    Neuromuscul Disord; 1996 Dec; 6(6):475-82. PubMed ID: 9027858
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  • 6. A novel gamma-sarcoglycan mutation causing childhood onset, slowly progressive limb girdle muscular dystrophy.
    van der Kooi AJ, de Visser M, van Meegen M, Ginjaar HB, van Essen AJ, Jennekens FG, Jongen PJ, Leschot NJ, Bolhuis PA.
    Neuromuscul Disord; 1998 Jun; 8(5):305-8. PubMed ID: 9673983
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  • 9. 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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  • 10. 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
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  • 12. Advances in the molecular genetics of the limb-girdle type of autosomal recessive progressive muscular dystrophy.
    Beckmann JS, Bushby KM.
    Curr Opin Neurol; 1996 Oct 22; 9(5):389-93. PubMed ID: 8894416
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  • 13. [The frequency of patients with adhalin deficiency in a muscular dystrophy patient population].
    Hayashi YK, Arahata K.
    Nihon Rinsho; 1997 Dec 22; 55(12):3165-8. PubMed ID: 9436429
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  • 15. A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families.
    Dinçer P, Akçören Z, Demir E, Richard I, Sancak O, Kale G, Ozme S, Karaduman A, Tan E, Urtizberea JA, Beckmann JS, Topaloğlu H.
    J Med Genet; 2000 May 22; 37(5):361-7. PubMed ID: 10807695
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  • 16. [Clinicopathological characteristics and molecular genetics of adhalin deficiency (severe childhood autosomal recessive muscular dystrophy/SCARMD)].
    Matsumura K.
    Nihon Rinsho; 1997 Dec 22; 55(12):3154-8. PubMed ID: 9436427
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  • 17. 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 22; 11(3):257-65. PubMed ID: 7581448
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  • 18. [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 22; 45(2):136-40. PubMed ID: 9120997
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  • 19. Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy.
    McNally EM, Duggan D, Gorospe JR, Bönnemann CG, Fanin M, Pegoraro E, Lidov HG, Noguchi S, Ozawa E, Finkel RS, Cruse RP, Angelini C, Kunkel LM, Hoffman EP.
    Hum Mol Genet; 1996 Nov 22; 5(11):1841-7. PubMed ID: 8923014
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  • 20. Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions.
    Crosbie RH, Lim LE, Moore SA, Hirano M, Hays AP, Maybaum SW, Collin H, Dovico SA, Stolle CA, Fardeau M, Tomé FM, Campbell KP.
    Hum Mol Genet; 2000 Aug 12; 9(13):2019-27. PubMed ID: 10942431
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