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Journal Abstract Search

220 related items for PubMed ID: 8776597

  • 21. Limb girdle muscular dystrophy in Manitoba Hutterites does not map to any of the known LGMD loci.
    Weiler T, Greenberg CR, Nylen E, Morgan K, Fujiwara TM, Crumley MJ, Zelinski T, Halliday W, Nickel B, Triggs-Raine B, Wrogemann K.
    Am J Med Genet; 1997 Oct 31; 72(3):363-8. PubMed ID: 9332671
    [Abstract] [Full Text] [Related]

  • 22. 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]

  • 23. A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21.
    Starling A, Kok F, Passos-Bueno MR, Vainzof M, Zatz M.
    Eur J Hum Genet; 2004 Dec 01; 12(12):1033-40. PubMed ID: 15367920
    [Abstract] [Full Text] [Related]

  • 24. Genetic basis of limb-girdle muscular dystrophies: the 2014 update.
    Nigro V, Savarese M.
    Acta Myol; 2014 May 01; 33(1):1-12. PubMed ID: 24843229
    [Abstract] [Full Text] [Related]

  • 25. Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy families.
    Speer MC, Vance JM, Lennon-Graham F, Stajich JM, Viles KD, Gilchrist JM, Nigro V, McMichael R, Chutkow JG, Bartoloni L, Horrigan SK, Westbrook CA, Pericak-Vance MA.
    Hum Hered; 1998 May 01; 48(4):179-84. PubMed ID: 9694248
    [Abstract] [Full Text] [Related]

  • 26. Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy.
    Jung D, Duclos F, Apostol B, Straub V, Lee JC, Allamand V, Venzke DP, Sunada Y, Moomaw CR, Leveille CJ, Slaughter CA, Crawford TO, McPherson JD, Campbell KP.
    J Biol Chem; 1996 Dec 13; 271(50):32321-9. PubMed ID: 8943294
    [Abstract] [Full Text] [Related]

  • 27. Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequence.
    Passos-Bueno MR, Terwilliger J, Ott J, Vainzof M, Love DR, Davies KE, Zatz M.
    Am J Med Genet; 1991 Jan 13; 38(1):140-6. PubMed ID: 2012126
    [Abstract] [Full Text] [Related]

  • 28. [Limb-girdle muscular dystrophy; update].
    Sunada Y.
    Rinsho Shinkeigaku; 2004 Nov 13; 44(11):995-7. PubMed ID: 15651352
    [Abstract] [Full Text] [Related]

  • 29. Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophy.
    Illarioshkin SN, Ivanova-Smolenskaya IA, Tanaka H, Vereshchagin NV, Markova ED, Poleshchuk VV, Lozhnikova SM, Sukhorukov VS, Limborska SA, Slominsky PA, Bulayeva KB, Tsuji S.
    Brain; 1996 Dec 13; 119 ( Pt 6)():1895-909. PubMed ID: 9009996
    [Abstract] [Full Text] [Related]

  • 30. Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21.
    van der Kooi AJ, van Meegen M, Ledderhof TM, McNally EM, de Visser M, Bolhuis PA.
    Am J Hum Genet; 1997 Apr 13; 60(4):891-5. PubMed ID: 9106535
    [Abstract] [Full Text] [Related]

  • 31. The 10 autosomal recessive limb-girdle muscular dystrophies.
    Zatz M, de Paula F, Starling A, Vainzof M.
    Neuromuscul Disord; 2003 Sep 13; 13(7-8):532-44. PubMed ID: 12921790
    [Abstract] [Full Text] [Related]

  • 32. [Clinical and genetic heterogeneity of limb-girdle muscular dystrophy].
    Kozłowska M.
    Neurol Neurochir Pol; 1995 Sep 13; 29(4):569-75. PubMed ID: 8544936
    [Abstract] [Full Text] [Related]

  • 33. Limb-girdle muscular dystrophy is closely linked to the fibrillin locus on chromosome 15.
    Velinov M, Sarfarazi M, Young K, Hodes ME, Conneally PM, Jackson CE, Tsipouras P.
    Connect Tissue Res; 1993 Sep 13; 29(1):13-21. PubMed ID: 8339542
    [Abstract] [Full Text] [Related]

  • 34.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Pegoraro E, Hoffman EP.
    ; 1993 Sep 13. PubMed ID: 20301582
    [Abstract] [Full Text] [Related]

  • 35. Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy.
    Speer MC, Gilchrist JM, Chutkow JG, McMichael R, Westbrook CA, Stajich JM, Jorgenson EM, Gaskell PC, Rosi BL, Ramesar R.
    Am J Hum Genet; 1995 Dec 13; 57(6):1371-6. PubMed ID: 8533766
    [Abstract] [Full Text] [Related]

  • 36. [Mapping of the gene for autosomal-recessive progressive muscular dystrophy in an isolate from a highland region of Dagestan to chromosome 2-13].
    Illarioshkin SN, Ivanova-Smolenskaia IA, Dimborskaia SA, Poleshchuk VV, Markova ED, Slominskiĭ PA, Bulaeva KB, Tsudzi Sh.
    Genetika; 1997 Nov 13; 33(11):1551-8. PubMed ID: 9480219
    [Abstract] [Full Text] [Related]

  • 37. 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 13; 8(3-4):193-7. PubMed ID: 9631401
    [Abstract] [Full Text] [Related]

  • 38. Autosomal dominant limb-girdle muscular dystrophy: a large kindred with evidence for anticipation.
    Gamez J, Navarro C, Andreu AL, Fernandez JM, Palenzuela L, Tejeira S, Fernandez-Hojas R, Schwartz S, Karadimas C, DiMauro S, Hirano M, Cervera C.
    Neurology; 2001 Feb 27; 56(4):450-4. PubMed ID: 11222786
    [Abstract] [Full Text] [Related]

  • 39. 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 27; 3(3):455-7. PubMed ID: 8012357
    [Abstract] [Full Text] [Related]

  • 40. 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 27; 37(5):361-7. PubMed ID: 10807695
    [Abstract] [Full Text] [Related]

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