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Journal Abstract Search

342 related items for PubMed ID: 15721128

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  • 2. High prevalence of exercise-induced arrhythmias in catecholaminergic polymorphic ventricular tachycardia mutation-positive family members diagnosed by cascade genetic screening.
    Haugaa KH, Leren IS, Berge KE, Bathen J, Loennechen JP, Anfinsen OG, Früh A, Edvardsen T, Kongsgård E, Leren TP, Amlie JP.
    Europace; 2010 Mar; 12(3):417-23. PubMed ID: 20106799
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  • 5. [Catecholaminergic polymorphic ventricular tachycardia].
    Leren IS, Haugaa KH, Edvardsen T, Anfinsen OG, Kongsgård E, Berge KE, Leren TP, Amlie JP.
    Tidsskr Nor Laegeforen; 2010 Jan 28; 130(2):139-42. PubMed ID: 20125202
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  • 7. Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients.
    Postma AV, Denjoy I, Kamblock J, Alders M, Lupoglazoff JM, Vaksmann G, Dubosq-Bidot L, Sebillon P, Mannens MM, Guicheney P, Wilde AA.
    J Med Genet; 2005 Nov 28; 42(11):863-70. PubMed ID: 16272262
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  • 9. A novel mutation (Arg169Gln) of the cardiac ryanodine receptor gene causing exercise-induced bidirectional ventricular tachycardia.
    Hsueh CH, Weng YC, Chen CY, Lin TK, Lin YH, Lai LP, Lin JL.
    Int J Cardiol; 2006 Apr 04; 108(2):276-8. PubMed ID: 16517285
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  • 11. Genetic characterization of familial CPVT after 30 years.
    Beery TA, Shah MJ, Benson DW.
    Biol Res Nurs; 2009 Jul 04; 11(1):66-72. PubMed ID: 19398417
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  • 13. Familial evaluation in catecholaminergic polymorphic ventricular tachycardia: disease penetrance and expression in cardiac ryanodine receptor mutation-carrying relatives.
    van der Werf C, Nederend I, Hofman N, van Geloven N, Ebink C, Frohn-Mulder IM, Alings AM, Bosker HA, Bracke FA, van den Heuvel F, Waalewijn RA, Bikker H, van Tintelen JP, Bhuiyan ZA, van den Berg MP, Wilde AA.
    Circ Arrhythm Electrophysiol; 2012 Aug 01; 5(4):748-56. PubMed ID: 22787013
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  • 15. Mutant ryanodine receptors in catecholaminergic polymorphic ventricular tachycardia generate delayed afterdepolarizations due to increased propensity to Ca2+ waves.
    Paavola J, Viitasalo M, Laitinen-Forsblom PJ, Pasternack M, Swan H, Tikkanen I, Toivonen L, Kontula K, Laine M.
    Eur Heart J; 2007 May 01; 28(9):1135-42. PubMed ID: 17347175
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  • 17. Catecholaminergic polymorphic ventricular tachycardia.
    Liu N, Ruan Y, Priori SG.
    Prog Cardiovasc Dis; 2008 May 01; 51(1):23-30. PubMed ID: 18634915
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  • 20. Postmortem molecular analysis for fatal arrhythmogenic disease in sudden unexplained death.
    Nishio H, Suzuki K.
    Leg Med (Tokyo); 2009 Apr 01; 11 Suppl 1():S119-20. PubMed ID: 19261510
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