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Journal Abstract Search

822 related items for PubMed ID: 17010805

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  • 23. Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations.
    Bauce B, Basso C, Rampazzo A, Beffagna G, Daliento L, Frigo G, Malacrida S, Settimo L, Danieli G, Thiene G, Nava A.
    Eur Heart J; 2005 Aug; 26(16):1666-75. PubMed ID: 15941723
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  • 24. Molecular insights into arrhythmogenic right ventricular cardiomyopathy caused by plakophilin-2 missense mutations.
    Kirchner F, Schuetz A, Boldt LH, Martens K, Dittmar G, Haverkamp W, Thierfelder L, Heinemann U, Gerull B.
    Circ Cardiovasc Genet; 2012 Aug 01; 5(4):400-11. PubMed ID: 22781308
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  • 27. The molecular genetics of arrhythmogenic right ventricular dysplasia-cardiomyopathy.
    Ahmad F.
    Clin Invest Med; 2003 Aug 01; 26(4):167-78. PubMed ID: 12934820
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  • 28. Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression.
    Sen-Chowdhry S, Syrris P, Ward D, Asimaki A, Sevdalis E, McKenna WJ.
    Circulation; 2007 Apr 03; 115(13):1710-20. PubMed ID: 17372169
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  • 30. Molecular genetics of arrhythmogenic right ventricular cardiomyopathy: emerging horizon?
    van Tintelen JP, Hofstra RM, Wiesfeld AC, van den Berg MP, Hauer RN, Jongbloed JD.
    Curr Opin Cardiol; 2007 May 03; 22(3):185-92. PubMed ID: 17413274
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  • 31. Arrhythmogenic right ventricular dysplasia/cardiomyopathy: pathogenic desmosome mutations in index-patients predict outcome of family screening: Dutch arrhythmogenic right ventricular dysplasia/cardiomyopathy genotype-phenotype follow-up study.
    Cox MG, van der Zwaag PA, van der Werf C, van der Smagt JJ, Noorman M, Bhuiyan ZA, Wiesfeld AC, Volders PG, van Langen IM, Atsma DE, Dooijes D, van den Wijngaard A, Houweling AC, Jongbloed JD, Jordaens L, Cramer MJ, Doevendans PA, de Bakker JM, Wilde AA, van Tintelen JP, Hauer RN.
    Circulation; 2011 Jun 14; 123(23):2690-700. PubMed ID: 21606396
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  • 33. Noninvasive detection of myocardial fibrosis in arrhythmogenic right ventricular cardiomyopathy using delayed-enhancement magnetic resonance imaging.
    Tandri H, Saranathan M, Rodriguez ER, Martinez C, Bomma C, Nasir K, Rosen B, Lima JA, Calkins H, Bluemke DA.
    J Am Coll Cardiol; 2005 Jan 04; 45(1):98-103. PubMed ID: 15629382
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  • 34. Functional assessment of potential splice site variants in arrhythmogenic right ventricular dysplasia/cardiomyopathy.
    Groeneweg JA, Ummels A, Mulder M, Bikker H, van der Smagt JJ, van Mil AM, Homfray T, Post JG, Elvan A, van der Heijden JF, Houweling AC, Jongbloed JD, Wilde AA, van Tintelen JP, Hauer RN, Dooijes D.
    Heart Rhythm; 2014 Nov 04; 11(11):2010-7. PubMed ID: 25087486
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  • 36. Clinical expression of plakophilin-2 mutations in familial arrhythmogenic right ventricular cardiomyopathy.
    Syrris P, Ward D, Asimaki A, Sen-Chowdhry S, Ebrahim HY, Evans A, Hitomi N, Norman M, Pantazis A, Shaw AL, Elliott PM, McKenna WJ.
    Circulation; 2006 Jan 24; 113(3):356-64. PubMed ID: 16415378
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  • 37. The value of different electrocardiographic depolarization criteria in the diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy.
    Peters S, Trümmel M, Koehler B, Westermann KU.
    J Electrocardiol; 2007 Jan 24; 40(1):34-7. PubMed ID: 17118392
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  • 38. Left-dominant arrhythmogenic cardiomyopathy in a large family: associated desmosomal or nondesmosomal genotype?
    Groeneweg JA, van der Zwaag PA, Jongbloed JD, Cox MG, Vreeker A, de Boer RA, van der Heijden JF, van Veen TA, McKenna WJ, van Tintelen JP, Dooijes D, Hauer RN.
    Heart Rhythm; 2013 Apr 24; 10(4):548-59. PubMed ID: 23270881
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  • 39. Plakophilin 2A is the dominant isoform in human heart tissue: consequences for the genetic screening of arrhythmogenic right ventricular cardiomyopathy.
    Gandjbakhch E, Charron P, Fressart V, Lorin de la Grandmaison G, Simon F, Gary F, Vite A, Hainque B, Hidden-Lucet F, Komajda M, Villard E.
    Heart; 2011 May 24; 97(10):844-9. PubMed ID: 21378009
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  • 40. Role of genetic testing in arrhythmogenic right ventricular cardiomyopathy/dysplasia.
    Barahona-Dussault C, Benito B, Campuzano O, Iglesias A, Leung TL, Robb L, Talajic M, Brugada R.
    Clin Genet; 2010 Jan 24; 77(1):37-48. PubMed ID: 19863551
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