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Journal Abstract Search

474 related items for PubMed ID: 17611253

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  • 3. Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes.
    Kaski JP, Syrris P, Burch M, Tomé-Esteban MT, Fenton M, Christiansen M, Andersen PS, Sebire N, Ashworth M, Deanfield JE, McKenna WJ, Elliott PM.
    Heart; 2008 Nov; 94(11):1478-84. PubMed ID: 18467357
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  • 6. The yield of risk stratification for sudden cardiac death in hypertrophic cardiomyopathy myosin-binding protein C gene mutation carriers: focus on predictive screening.
    Christiaans I, Birnie E, van Langen IM, van Spaendonck-Zwarts KY, van Tintelen JP, van den Berg MP, Atsma DE, Helderman-van den Enden AT, Pinto YM, Hermans-van Ast JF, Bonsel GJ, Wilde AA.
    Eur Heart J; 2010 Apr; 31(7):842-8. PubMed ID: 20019025
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  • 9. Mutation of Arg723Gly in beta-myosin heavy chain gene in five Chinese families with hypertrophic cardiomyopathy.
    Yang JH, Zheng DD, Dong NZ, Yang XJ, Song JP, Jiang TB, Cheng XJ, Li HX, Zhou BY, Zhao CM, Jiang WP.
    Chin Med J (Engl); 2006 Nov 05; 119(21):1785-9. PubMed ID: 17097032
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  • 10. Disease penetrance and risk stratification for sudden cardiac death in asymptomatic hypertrophic cardiomyopathy mutation carriers.
    Michels M, Soliman OI, Phefferkorn J, Hoedemaekers YM, Kofflard MJ, Dooijes D, Majoor-Krakauer D, Ten Cate FJ.
    Eur Heart J; 2009 Nov 05; 30(21):2593-8. PubMed ID: 19666645
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  • 11. Natural history and familial characteristics of isolated left ventricular non-compaction.
    Murphy RT, Thaman R, Blanes JG, Ward D, Sevdalis E, Papra E, Kiotsekoglou A, Tome MT, Pellerin D, McKenna WJ, Elliott PM.
    Eur Heart J; 2005 Jan 05; 26(2):187-92. PubMed ID: 15618076
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  • 12. Prevalence of sarcomere protein gene mutations in preadolescent children with hypertrophic cardiomyopathy.
    Kaski JP, Syrris P, Esteban MT, Jenkins S, Pantazis A, Deanfield JE, McKenna WJ, Elliott PM.
    Circ Cardiovasc Genet; 2009 Oct 05; 2(5):436-41. PubMed ID: 20031618
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  • 13. Left ventricular non-compaction revisited: a distinct phenotype with genetic heterogeneity?
    Oechslin E, Jenni R.
    Eur Heart J; 2011 Jun 05; 32(12):1446-56. PubMed ID: 21285074
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  • 14. Diagnosis of left-ventricular non-compaction in patients with left-ventricular systolic dysfunction: time for a reappraisal of diagnostic criteria?
    Kohli SK, Pantazis AA, Shah JS, Adeyemi B, Jackson G, McKenna WJ, Sharma S, Elliott PM.
    Eur Heart J; 2008 Jan 05; 29(1):89-95. PubMed ID: 17993472
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  • 15. Severe familial left ventricular non-compaction cardiomyopathy due to a novel troponin T (TNNT2) mutation.
    Luedde M, Ehlermann P, Weichenhan D, Will R, Zeller R, Rupp S, Müller A, Steen H, Ivandic BT, Ulmer HE, Kern M, Katus HA, Frey N.
    Cardiovasc Res; 2010 Jun 01; 86(3):452-60. PubMed ID: 20083571
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  • 16. Mutations in sarcomere protein genes in left ventricular noncompaction.
    Klaassen S, Probst S, Oechslin E, Gerull B, Krings G, Schuler P, Greutmann M, Hürlimann D, Yegitbasi M, Pons L, Gramlich M, Drenckhahn JD, Heuser A, Berger F, Jenni R, Thierfelder L.
    Circulation; 2008 Jun 03; 117(22):2893-901. PubMed ID: 18506004
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  • 17. Familial and sporadic hypertrophic myopathy: differences and similarities in a genotyped population. A long follow-up study.
    Brito D, Richard P, Komajda M, Madeira H.
    Rev Port Cardiol; 2008 Feb 03; 27(2):147-73. PubMed ID: 18488914
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  • 18. Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene.
    Villard E, Duboscq-Bidot L, Charron P, Benaiche A, Conraads V, Sylvius N, Komajda M.
    Eur Heart J; 2005 Apr 03; 26(8):794-803. PubMed ID: 15769782
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  • 19. Novel troponin T mutation in familial dilated cardiomyopathy with gender-dependant severity.
    Stefanelli CB, Rosenthal A, Borisov AB, Ensing GJ, Russell MW.
    Mol Genet Metab; 2004 Apr 03; 83(1-2):188-96. PubMed ID: 15464434
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  • 20. Left ventricular noncompaction associated with hypertrophic cardiomyopathy: echocardiographic diagnosis and genetic analysis of a new pedigree in China.
    Yuan L, Xie M, Cheng TO, Wang X, Zhu F, Kong X, Ghoorah D.
    Int J Cardiol; 2014 Jun 15; 174(2):249-59. PubMed ID: 24698237
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