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Journal Abstract Search

253 related items for PubMed ID: 10655062

  • 1. Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin.
    Moreira ES, Wiltshire TJ, Faulkner G, Nilforoushan A, Vainzof M, Suzuki OT, Valle G, Reeves R, Zatz M, Passos-Bueno MR, Jenne DE.
    Nat Genet; 2000 Feb; 24(2):163-6. PubMed ID: 10655062
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  • 2. Dysferlin protein analysis in limb-girdle muscular dystrophies.
    Vainzof M, Anderson LV, McNally EM, Davis DB, Faulkner G, Valle G, Moreira ES, Pavanello RC, Passos-Bueno MR, Zatz M.
    J Mol Neurosci; 2001 Aug; 17(1):71-80. PubMed ID: 11665864
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  • 3. Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G.
    Passos-Bueno MR, Vainzof M, Moreira ES, Zatz M.
    Am J Med Genet; 1999 Feb 19; 82(5):392-8. PubMed ID: 10069710
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  • 6. Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMD.
    Passos-Bueno MR, Moreira ES, Vainzof M, Marie SK, Zatz M.
    Hum Mol Genet; 1996 Jun 19; 5(6):815-20. PubMed ID: 8776597
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  • 8. Molecular bases of autosomal recessive limb-girdle muscular dystrophies.
    Nigro V.
    Acta Myol; 2003 Sep 19; 22(2):35-42. PubMed ID: 14959561
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  • 9. 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 19; 14(2):195-8. PubMed ID: 8841194
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  • 10. Telethonin protein expression in neuromuscular disorders.
    Vainzof M, Moreira ES, Suzuki OT, Faulkner G, Valle G, Beggs AH, Carpen O, Ribeiro AF, Zanoteli E, Gurgel-Gianneti J, Tsanaclis AM, Silva HC, Passos-Bueno MR, Zatz M.
    Biochim Biophys Acta; 2002 Oct 09; 1588(1):33-40. PubMed ID: 12379311
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  • 12. A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus.
    Weiler T, Greenberg CR, Zelinski T, Nylen E, Coghlan G, Crumley MJ, Fujiwara TM, Morgan K, Wrogemann K.
    Am J Hum Genet; 1998 Jul 09; 63(1):140-7. PubMed ID: 9634523
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  • 15. LGMD 2E in Tunisia is caused by a homozygous missense mutation in beta-sarcoglycan exon 3.
    Bönnemann CG, Wong J, Ben Hamida C, Hamida MB, Hentati F, Kunkel LM.
    Neuromuscul Disord; 1998 May 09; 8(3-4):193-7. PubMed ID: 9631401
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  • 16. 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 09; 35(11):951-3. PubMed ID: 9832045
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  • 18. The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12.
    Moreira ES, Vainzof M, Marie SK, Sertié AL, Zatz M, Passos-Bueno MR.
    Am J Hum Genet; 1997 Jul 09; 61(1):151-9. PubMed ID: 9245996
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  • 19. Myotilin, a novel sarcomeric protein with two Ig-like domains, is encoded by a candidate gene for limb-girdle muscular dystrophy.
    Salmikangas P, Mykkänen OM, Grönholm M, Heiska L, Kere J, Carpén O.
    Hum Mol Genet; 1999 Jul 09; 8(7):1329-36. PubMed ID: 10369880
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