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Journal Abstract Search

84 related items for PubMed ID: 12806729

  • 1. [A new type of myotonic dystrophy].
    Auvinen S, Vihola A, Krahe R, Kupila J, Hackman P, Hietaharju A, Udd B.
    Duodecim; 2003; 119(8):707-13. PubMed ID: 12806729
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  • 2. Homozygosity for CCTG mutation in myotonic dystrophy type 2.
    Schoser BG, Kress W, Walter MC, Halliger-Keller B, Lochmüller H, Ricker K.
    Brain; 2004 Aug; 127(Pt 8):1868-77. PubMed ID: 15231584
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  • 3. [From gene to disease; altered RNA processing as a cause of myotonic dystrophy type 1].
    de Die-Smulders CE, Faber CG, Smeets HJ.
    Ned Tijdschr Geneeskd; 2005 Sep 10; 149(37):2043-6. PubMed ID: 16184945
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  • 4. Biomedicine. Reconstructing myotonic dystrophy.
    Tapscott SJ, Thornton CA.
    Science; 2001 Aug 03; 293(5531):816-7. PubMed ID: 11486078
    [No Abstract] [Full Text] [Related]

  • 5. Myotonic dystrophies type 1 and 2: a summary on current aspects.
    Schara U, Schoser BG.
    Semin Pediatr Neurol; 2006 Jun 03; 13(2):71-9. PubMed ID: 17027856
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  • 6. Myotonic dystrophies--how many are there?
    Mastaglia FL.
    Curr Opin Neurol; 1999 Oct 03; 12(5):491-2. PubMed ID: 10590884
    [No Abstract] [Full Text] [Related]

  • 7. [Molecular and genetic aspects of the myotonic conditions].
    Morales Montero F, Cuenca Berger P.
    Rev Neurol; 1999 Oct 03; 38(7):668-74. PubMed ID: 15098190
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  • 8. Outcome and effect of pregnancy in myotonic dystrophy type 2.
    Rudnik-Schöneborn S, Schneider-Gold C, Raabe U, Kress W, Zerres K, Schoser BG.
    Neurology; 2006 Feb 28; 66(4):579-80. PubMed ID: 16505316
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  • 11. New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2).
    Sallinen R, Vihola A, Bachinski LL, Huoponen K, Haapasalo H, Hackman P, Zhang S, Sirito M, Kalimo H, Meola G, Horelli-Kuitunen N, Wessman M, Krahe R, Udd B.
    Neuromuscul Disord; 2004 Apr 28; 14(4):274-83. PubMed ID: 15019706
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  • 12. Colocalization of muscleblind with RNA foci is separable from mis-regulation of alternative splicing in myotonic dystrophy.
    Ho TH, Savkur RS, Poulos MG, Mancini MA, Swanson MS, Cooper TA.
    J Cell Sci; 2005 Jul 01; 118(Pt 13):2923-33. PubMed ID: 15961406
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  • 17. Myotonic dystrophy type 2 with focal asymmetric muscle weakness and no electrical myotonia.
    Milone M, Batish SD, Daube JR.
    Muscle Nerve; 2009 Mar 01; 39(3):383-5. PubMed ID: 19208413
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  • 18. Unusual clinical, laboratory, and muscle histopathological findings in a family with myotonic dystrophy type 2.
    Toth C, Dunham C, Suchowersky O, Parboosingh J, Brownell K.
    Muscle Nerve; 2007 Feb 01; 35(2):259-64. PubMed ID: 17068784
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  • 19. [Myotonic dystrophy as an RNA-mediated disease].
    Ishiura S.
    Rinsho Shinkeigaku; 2005 Nov 01; 45(11):828-30. PubMed ID: 16447737
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  • 20. Inheritance of a novel RYR1 mutation in a family with myotonic dystrophy type 1.
    Gambelli S, Malandrini A, Berti G, Gaudiano C, Zicari E, Brunori P, Perticoni G, Orrico A, Galli L, Sorrentino V, Lunardi J, Federico A, Dotti MT.
    Clin Genet; 2007 Jan 01; 71(1):93-4. PubMed ID: 17204054
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