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Journal Abstract Search

249 related items for PubMed ID: 20206892

  • 1. Familial dilated cardiomyopathy secondary to dystrophin splice site mutation.
    Obler D, Wu BL, Lip V, Estrella E, Keck S, Haggan C, Semigran M, Smoot LB.
    J Card Fail; 2010 Mar; 16(3):194-9. PubMed ID: 20206892
    [Abstract] [Full Text] [Related]

  • 2. [Familial dilated cardiomyopathy].
    Osterziel KJ, Hassfeld S, Geier C, Perrot A.
    Herz; 2005 Sep; 30(6):529-34. PubMed ID: 16170685
    [Abstract] [Full Text] [Related]

  • 3. A 5' dystrophin duplication mutation causes membrane deficiency of alpha-dystroglycan in a family with X-linked cardiomyopathy.
    Bies RD, Maeda M, Roberds SL, Holder E, Bohlmeyer T, Young JB, Campbell KP.
    J Mol Cell Cardiol; 1997 Dec; 29(12):3175-88. PubMed ID: 9441825
    [Abstract] [Full Text] [Related]

  • 4. Novel mutation in splicing donor of dystrophin gene first exon in a patient with dilated cardiomyopathy but no clinical signs of skeletal myopathy.
    Kimura S, Ikezawa M, Ozasa S, Ito K, Ueno H, Yoshioka K, Ijiri S, Nomura K, Nakamura K, Matuskura M, Miike T.
    J Child Neurol; 2007 Jul; 22(7):901-6. PubMed ID: 17715288
    [Abstract] [Full Text] [Related]

  • 5. Familial dilated cardiomyopathy with troponin T K210del mutation.
    Martins E, Silva-Cardoso J, Alves C, Pereira H, Soares B, Damasceno A, Abreu-Lima C, Amorim A, Rocha-Gonçalves F.
    Rev Port Cardiol; 2006 Mar; 25(3):295-300. PubMed ID: 16789403
    [Abstract] [Full Text] [Related]

  • 6. High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics.
    van Tintelen JP, Hofstra RM, Katerberg H, Rossenbacker T, Wiesfeld AC, du Marchie Sarvaas GJ, Wilde AA, van Langen IM, Nannenberg EA, van der Kooi AJ, Kraak M, van Gelder IC, van Veldhuisen DJ, Vos Y, van den Berg MP, Working Group on Inherited Cardiac Disorders, line 27/50, Interuniversity Cardiology Institute of The Netherlands.
    Am Heart J; 2007 Dec; 154(6):1130-9. PubMed ID: 18035086
    [Abstract] [Full Text] [Related]

  • 7. Diagnostic work-up and risk stratification in X-linked dilated cardiomyopathies caused by dystrophin defects.
    Diegoli M, Grasso M, Favalli V, Serio A, Gambarin FI, Klersy C, Pasotti M, Agozzino E, Scelsi L, Ferlini A, Febo O, Piccolo G, Tavazzi L, Narula J, Arbustini E.
    J Am Coll Cardiol; 2011 Aug 23; 58(9):925-34. PubMed ID: 21851881
    [Abstract] [Full Text] [Related]

  • 8. Inflammatory dilated cardiomyopathy (DCMI).
    Maisch B, Richter A, Sandmöller A, Portig I, Pankuweit S, BMBF-Heart Failure Network.
    Herz; 2005 Sep 23; 30(6):535-44. PubMed ID: 16170686
    [Abstract] [Full Text] [Related]

  • 9. Genetic predictors and remodeling of dilated cardiomyopathy in muscular dystrophy.
    Jefferies JL, Eidem BW, Belmont JW, Craigen WJ, Ware SM, Fernbach SD, Neish SR, Smith EO, Towbin JA.
    Circulation; 2005 Nov 01; 112(18):2799-804. PubMed ID: 16246949
    [Abstract] [Full Text] [Related]

  • 10. Current perspective new insights into the molecular basis of familial dilated cardiomyopathy.
    Sinagra G, Di Lenarda A, Brodsky GL, Taylor MR, Muntoni F, Pinamonti B, Carniel E, Driussi M, Bristow MR, Mestroni L, Heart Muscle Disease Study Group.
    Ital Heart J; 2001 Apr 01; 2(4):280-6. PubMed ID: 11374497
    [Abstract] [Full Text] [Related]

  • 11. Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy.
    Millat G, Bouvagnet P, Chevalier P, Sebbag L, Dulac A, Dauphin C, Jouk PS, Delrue MA, Thambo JB, Le Metayer P, Seronde MF, Faivre L, Eicher JC, Rousson R.
    Eur J Med Genet; 2011 Apr 01; 54(6):e570-5. PubMed ID: 21846512
    [Abstract] [Full Text] [Related]

  • 12. Thymopoietin (lamina-associated polypeptide 2) gene mutation associated with dilated cardiomyopathy.
    Taylor MR, Slavov D, Gajewski A, Vlcek S, Ku L, Fain PR, Carniel E, Di Lenarda A, Sinagra G, Boucek MM, Cavanaugh J, Graw SL, Ruegg P, Feiger J, Zhu X, Ferguson DA, Bristow MR, Gotzmann J, Foisner R, Mestroni L, Familial Cardiomyopathy Registry Research Group.
    Hum Mutat; 2005 Dec 01; 26(6):566-74. PubMed ID: 16247757
    [Abstract] [Full Text] [Related]

  • 13. Identification of a point mutation and germinal mosaicism in a Duchenne muscular dystrophy family.
    Wilton SD, Chandler DC, Kakulas BA, Laing NG.
    Hum Mutat; 1994 Dec 01; 3(2):133-40. PubMed ID: 8199594
    [Abstract] [Full Text] [Related]

  • 14. R25G mutation in exon 1 of LMNA gene is associated with dilated cardiomyopathy and limb-girdle muscular dystrophy 1B.
    Yuan WL, Huang CY, Wang JF, Xie SL, Nie RQ, Liu YM, Liu PM, Zhou SX, Chen SQ, Huang WJ.
    Chin Med J (Engl); 2009 Dec 05; 122(23):2840-5. PubMed ID: 20092787
    [Abstract] [Full Text] [Related]

  • 15. [Genetic diagnosis of familial dilated cardiomyopathy].
    Pasotti M, Repetto A, Pisani A, Arbustini E.
    Ital Heart J Suppl; 2002 Apr 05; 3(4):386-93. PubMed ID: 12025381
    [Abstract] [Full Text] [Related]

  • 16. Functional consequences of an LMNA mutation associated with a new cardiac and non-cardiac phenotype.
    Charniot JC, Pascal C, Bouchier C, Sébillon P, Salama J, Duboscq-Bidot L, Peuchmaurd M, Desnos M, Artigou JY, Komajda M.
    Hum Mutat; 2003 May 05; 21(5):473-81. PubMed ID: 12673789
    [Abstract] [Full Text] [Related]

  • 17. Dilated cardiomyopathy caused by LMNA mutations. Clinical and morphological studies.
    Bilińska ZT, Sylvius N, Grzybowski J, Fidziańska A, Michalak E, Walczak E, Walski M, Bieganowska K, Szymaniak E, Kuśmierczyk-Droszcz B, Lubiszewska B, Wagner T, Tesson F, Ruzyłło W.
    Kardiol Pol; 2006 Aug 05; 64(8):812-9; discussion 820-1. PubMed ID: 16981056
    [Abstract] [Full Text] [Related]

  • 18. A novel mutation, Ser143Pro, in the lamin A/C gene is common in finnish patients with familial dilated cardiomyopathy.
    Kärkkäinen S, Heliö T, Miettinen R, Tuomainen P, Peltola P, Rummukainen J, Ylitalo K, Kaartinen M, Kuusisto J, Toivonen L, Nieminen MS, Laakso M, Peuhkurinen K.
    Eur Heart J; 2004 May 05; 25(10):885-93. PubMed ID: 15140538
    [Abstract] [Full Text] [Related]

  • 19. A point mutation in the 5' splice site of the dystrophin gene first intron responsible for X-linked dilated cardiomyopathy.
    Milasin J, Muntoni F, Severini GM, Bartoloni L, Vatta M, Krajinovic M, Mateddu A, Angelini C, Camerini F, Falaschi A, Mestroni L, Giacca M.
    Hum Mol Genet; 1996 Jan 05; 5(1):73-9. PubMed ID: 8789442
    [Abstract] [Full Text] [Related]

  • 20. Familial dilated cardiomyopathy: evidence for clinical and immunogenetic heterogeneity.
    Bilińska ZT, Michalak E, Piatosa B, Grzybowski J, Skwarek M, Deptuch TW, Kuśmierczyk-Droszcz B, Piotrowski W, Ruzyłło W.
    Med Sci Monit; 2003 May 05; 9(5):CR167-74. PubMed ID: 12761452
    [Abstract] [Full Text] [Related]

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