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Journal Abstract Search

136 related items for PubMed ID: 8899051

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy.
    Bueno MR, Moreira ES, Vainzof M, Chamberlain J, Marie SK, Pereira L, Akiyama J, Roberds SL, Campbell KP, Zatz M.
    Hum Mol Genet; 1995 Jul; 4(7):1163-7. PubMed ID: 8528203
    [Abstract] [Full Text] [Related]

  • 3. Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families.
    Passos-Bueno MR, Moreira ES, Marie SK, Bashir R, Vasquez L, Love DR, Vainzof M, Iughetti P, Oliveira JR, Bakker E, Strachan T, Bushby K, Zatz M.
    J Med Genet; 1996 Feb; 33(2):97-102. PubMed ID: 8929943
    [Abstract] [Full Text] [Related]

  • 4. 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; 5(6):815-20. PubMed ID: 8776597
    [Abstract] [Full Text] [Related]

  • 5. 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; 14(2):195-8. PubMed ID: 8841194
    [Abstract] [Full Text] [Related]

  • 6. A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey.
    Dinçer P, Leturcq F, Richard I, Piccolo F, Yalnizoglu D, de Toma C, Akçören Z, Broux O, Deburgrave N, Brenguier L, Roudaut C, Urtizberea JA, Jung D, Tan E, Jeanpierre M, Campbell KP, Kaplan JC, Beckmann JS, Topaloglu H.
    Ann Neurol; 1997 Aug; 42(2):222-9. PubMed ID: 9266733
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. Limb girdle muscular dystrophy: reappraisal of a rejected entity.
    van der Kooi AJ, de Visser M, Barth PG.
    Clin Neurol Neurosurg; 1994 Aug 19; 96(3):209-18. PubMed ID: 7988088
    [Abstract] [Full Text] [Related]

  • 9. Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (LGMD2B) in three families allows refinement of the candidate region.
    Passos-Bueno MR, Bashir R, Moreira ES, Vainzof M, Marie SK, Vasquez L, Iughetti P, Bakker E, Keers S, Stephenson A.
    Genomics; 1995 May 01; 27(1):192-5. PubMed ID: 7665169
    [Abstract] [Full Text] [Related]

  • 10. A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p.
    Bashir R, Strachan T, Keers S, Stephenson A, Mahjneh I, Marconi G, Nashef L, Bushby KM.
    Hum Mol Genet; 1994 Mar 01; 3(3):455-7. PubMed ID: 8012357
    [Abstract] [Full Text] [Related]

  • 11. 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 01; 61(1):151-9. PubMed ID: 9245996
    [Abstract] [Full Text] [Related]

  • 12. Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q.
    Speer MC, Yamaoka LH, Gilchrist JH, Gaskell CP, Stajich JM, Vance JM, Kazantsev A, Lastra AA, Haynes CS, Beckmann JS.
    Am J Hum Genet; 1992 Jun 01; 50(6):1211-7. PubMed ID: 1598902
    [Abstract] [Full Text] [Related]

  • 13. Understanding the heterogeneity of the limb-girdle muscular dystrophies.
    Bushby K.
    Biochem Soc Trans; 1996 May 01; 24(2):489-96. PubMed ID: 8736790
    [No Abstract] [Full Text] [Related]

  • 14. [Clinical and genetic heterogeneity of limb-girdle muscular dystrophy].
    Kozłowska M.
    Neurol Neurochir Pol; 1995 May 01; 29(4):569-75. PubMed ID: 8544936
    [Abstract] [Full Text] [Related]

  • 15. Refined genetic location of the chromosome 2p-linked progressive muscular dystrophy gene.
    Illarioshkin SN, Ivanova-Smolenskaya IA, Tanaka H, Poleshchuk VV, Markova ED, Tsuji S.
    Genomics; 1997 Jun 01; 42(2):345-8. PubMed ID: 9192858
    [Abstract] [Full Text] [Related]

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  • 17. 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 01; 63(1):140-7. PubMed ID: 9634523
    [Abstract] [Full Text] [Related]

  • 18. Facioscapulohumeral muscular dystrophy: the impact of genetic research.
    Brouwer OF, Wijmenga C, Frants RR, Padberg GW.
    Clin Neurol Neurosurg; 1993 Mar 01; 95(1):9-21. PubMed ID: 8095870
    [Abstract] [Full Text] [Related]

  • 19. 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
    [Abstract] [Full Text] [Related]

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