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Journal Abstract Search

510 related items for PubMed ID: 22677073

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  • 5. Unexplained drownings and the cardiac channelopathies: a molecular autopsy series.
    Tester DJ, Medeiros-Domingo A, Will ML, Ackerman MJ.
    Mayo Clin Proc; 2011 Oct; 86(10):941-7. PubMed ID: 21964171
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  • 6. The prevalence of mutations in KCNQ1, KCNH2, and SCN5A in an unselected national cohort of young sudden unexplained death cases.
    Winkel BG, Larsen MK, Berge KE, Leren TP, Nissen PH, Olesen MS, Hollegaard MV, Jespersen T, Yuan L, Nielsen N, Haunsø S, Svendsen JH, Wang Y, Kristensen IB, Jensen HK, Tfelt-Hansen J, Banner J.
    J Cardiovasc Electrophysiol; 2012 Oct; 23(10):1092-8. PubMed ID: 22882672
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  • 7. 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; 79(11):1380-4. PubMed ID: 15544015
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  • 8. Long QT and Brugada syndrome gene mutations in New Zealand.
    Chung SK, MacCormick JM, McCulley CH, Crawford J, Eddy CA, Mitchell EA, Shelling AN, French JK, Skinner JR, Rees MI.
    Heart Rhythm; 2007 Oct; 4(10):1306-14. PubMed ID: 17905336
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  • 9. Mutations in the SCN5A gene: evidence for a link between long QT syndrome and sudden death?
    Kiehne N, Kauferstein S.
    Forensic Sci Int Genet; 2007 Jun; 1(2):170-4. PubMed ID: 19083750
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  • 10. Prospective, population-based long QT molecular autopsy study of postmortem negative sudden death in 1 to 40 year olds.
    Skinner JR, Crawford J, Smith W, Aitken A, Heaven D, Evans CA, Hayes I, Neas KR, Stables S, Koelmeyer T, Denmark L, Vuletic J, Maxwell F, White K, Yang T, Roden DM, Leren TP, Shelling A, Love DR, Cardiac Inherited Disease Group New Zealand.
    Heart Rhythm; 2011 Mar; 8(3):412-9. PubMed ID: 21070882
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  • 11. Allelic dropout in long QT syndrome genetic testing: a possible mechanism underlying false-negative results.
    Tester DJ, Cronk LB, Carr JL, Schulz V, Salisbury BA, Judson RS, Ackerman MJ.
    Heart Rhythm; 2006 Jul; 3(7):815-21. PubMed ID: 16818214
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  • 12. 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; 130(1):59-66. PubMed ID: 26228265
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  • 13. Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.
    Tester DJ, Will ML, Haglund CM, Ackerman MJ.
    Heart Rhythm; 2005 May; 2(5):507-17. PubMed ID: 15840476
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  • 14. Long QT syndrome-associated mutations in intrauterine fetal death.
    Crotti L, Tester DJ, White WM, Bartos DC, Insolia R, Besana A, Kunic JD, Will ML, Velasco EJ, Bair JJ, Ghidoni A, Cetin I, Van Dyke DL, Wick MJ, Brost B, Delisle BP, Facchinetti F, George AL, Schwartz PJ, Ackerman MJ.
    JAMA; 2013 Apr 10; 309(14):1473-82. PubMed ID: 23571586
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  • 17. Investigation of ion channel gene variants in patients with long QT syndrome.
    Ernesto C, Cruz FE, Lima FS, Coutinho JL, Silva R, Urményi TP, Carvalho AC, Rondinelli E.
    Arq Bras Cardiol; 2011 Mar 10; 96(3):172-8. PubMed ID: 21308345
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  • 19. Targeted next generation sequencing application in cardiac channelopathies: Analysis of a cohort of autopsy-negative sudden unexplained deaths.
    Farrugia A, Keyser C, Hollard C, Raul JS, Muller J, Ludes B.
    Forensic Sci Int; 2015 Sep 10; 254():5-11. PubMed ID: 26164358
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  • 20. Mutation screening in KCNQ1, HERG, KCNE1, KCNE2 and SCN5A genes in a long QT syndrome family.
    Koo SH, Teo WS, Ching CK, Chan SH, Lee EJ.
    Ann Acad Med Singap; 2007 Jun 10; 36(6):394-8. PubMed ID: 17597962
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