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204 related items for PubMed ID: 19261510

  • 1. Postmortem molecular analysis for fatal arrhythmogenic disease in sudden unexplained death.
    Nishio H, Suzuki K.
    Leg Med (Tokyo); 2009 Apr; 11 Suppl 1():S119-20. PubMed ID: 19261510
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  • 2. Postmortem long QT syndrome genetic testing for sudden unexplained death in the young.
    Tester DJ, Ackerman MJ.
    J Am Coll Cardiol; 2007 Jan 16; 49(2):240-6. PubMed ID: 17222736
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  • 3. Identification of a novel mutation V2321M of the cardiac ryanodine receptor gene of sudden unexplained death and a phenotypic study of the gene mutations.
    Nishio H, Iwata M, Tamura A, Miyazaki T, Tsuboi K, Suzuki K.
    Leg Med (Tokyo); 2008 Jul 16; 10(4):196-200. PubMed ID: 18262818
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  • 4. Genetic screening in sudden cardiac death in the young can save future lives.
    Stattin EL, Westin IM, Cederquist K, Jonasson J, Jonsson BA, Mörner S, Norberg A, Krantz P, Wisten A.
    Int J Legal Med; 2016 Jan 16; 130(1):59-66. PubMed ID: 26228265
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  • 5. Targeted mutational analysis of the RyR2-encoded cardiac ryanodine receptor in sudden unexplained death: a molecular autopsy of 49 medical examiner/coroner's cases.
    Tester DJ, Spoon DB, Valdivia HH, Makielski JC, Ackerman MJ.
    Mayo Clin Proc; 2004 Nov 16; 79(11):1380-4. PubMed ID: 15544015
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  • 6. Molecular genetics of exercise-induced polymorphic ventricular tachycardia: identification of three novel cardiac ryanodine receptor mutations and two common calsequestrin 2 amino-acid polymorphisms.
    Laitinen PJ, Swan H, Kontula K.
    Eur J Hum Genet; 2003 Nov 16; 11(11):888-91. PubMed ID: 14571276
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  • 7. Dual inheritance of sudden death from cardiovascular causes.
    Beckmann BM, Wilde AA, Kääb S.
    N Engl J Med; 2008 May 08; 358(19):2077-8. PubMed ID: 18463390
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  • 10. 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 08; 42(11):863-70. PubMed ID: 16272262
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  • 11. Spectrum and prevalence of cardiac ryanodine receptor (RyR2) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testing.
    Tester DJ, Kopplin LJ, Will ML, Ackerman MJ.
    Heart Rhythm; 2005 Oct 08; 2(10):1099-105. PubMed ID: 16188589
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  • 13. Unusual clinical presentation in a family with catecholaminergic polymorphic ventricular tachycardia due to a G14876A ryanodine receptor gene mutation.
    Allouis M, Probst V, Jaafar P, Schott JJ, Le Marec H.
    Am J Cardiol; 2005 Mar 01; 95(5):700-2. PubMed ID: 15721128
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  • 16. Catecholaminergic polymorphic ventricular tachycardia from bedside to bench and beyond.
    Katz G, Arad M, Eldar M.
    Curr Probl Cardiol; 2009 Jan 01; 34(1):9-43. PubMed ID: 19068246
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  • 20. A case of catecholaminergic polymorphic ventricular tachycardia caused by two calsequestrin 2 mutations.
    de la Fuente S, Van Langen IM, Postma AV, Bikker H, Meijer A.
    Pacing Clin Electrophysiol; 2008 Jul 01; 31(7):916-9. PubMed ID: 18684293
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