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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

220 related items for PubMed ID: 8776597

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  • 7. Molecular bases of autosomal recessive limb-girdle muscular dystrophies.
    Nigro V.
    Acta Myol; 2003 Sep; 22(2):35-42. PubMed ID: 14959561
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  • 10. Limb-girdle muscular dystrophy: a follow-up study of 79 patients.
    Mahjneh I, Bushby K, Pizzi A, Bashir R, Marconi G.
    Acta Neurol Scand; 1996 Sep; 94(3):177-89. PubMed ID: 8899051
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  • 11. A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies.
    Moreira ES, Vainzof M, Marie SK, Nigro V, Zatz M, Passos-Bueno MR.
    J Med Genet; 1998 Nov; 35(11):951-3. PubMed ID: 9832045
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  • 13. [Limb girdle muscular dystrophies].
    Finsterer J.
    Nervenarzt; 2004 Dec; 75(12):1153-66. PubMed ID: 15316618
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  • 14. A diagnostic fluorescent marker kit for six limb girdle muscular dystrophies.
    Richard I, Bourg N, Marchand S, Alibert O, Eymard B, van der Kooi AJ, Jackson CE, Garcia C, Burgunder JM, Legum C, de Visser M, Fardeau M, Beckmann JS.
    Neuromuscul Disord; 1999 Dec; 9(8):555-63. PubMed ID: 10619713
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  • 16. Genetic and physical mapping at the limb-girdle muscular dystrophy locus (LGMD2B) on chromosome 2p.
    Bashir R, Keers S, Strachan T, Passos-Bueno R, Zatz M, Weissenbach J, Le Paslier D, Meisler M, Bushby K.
    Genomics; 1996 Apr 01; 33(1):46-52. PubMed ID: 8617508
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