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PUBMED FOR HANDHELDS

Journal Abstract Search


1129 related items for PubMed ID: 17222736

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  • 3. 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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  • 4. Long QT syndrome in adults.
    Sauer AJ, Moss AJ, McNitt S, Peterson DR, Zareba W, Robinson JL, Qi M, Goldenberg I, Hobbs JB, Ackerman MJ, Benhorin J, Hall WJ, Kaufman ES, Locati EH, Napolitano C, Priori SG, Schwartz PJ, Towbin JA, Vincent GM, Zhang L.
    J Am Coll Cardiol; 2007 Jan 23; 49(3):329-37. PubMed ID: 17239714
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  • 5. 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 23; 2(10):1099-105. PubMed ID: 16188589
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  • 9. Pathogenesis of unexplained drowning: new insights from a molecular autopsy.
    Tester DJ, Kopplin LJ, Creighton W, Burke AP, Ackerman MJ.
    Mayo Clin Proc; 2005 May 23; 80(5):596-600. PubMed ID: 15887426
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  • 11. 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 23; 2(5):507-17. PubMed ID: 15840476
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  • 12. Targeted mutational analysis of ankyrin-B in 541 consecutive, unrelated patients referred for long QT syndrome genetic testing and 200 healthy subjects.
    Sherman J, Tester DJ, Ackerman MJ.
    Heart Rhythm; 2005 Nov 23; 2(11):1218-23. PubMed ID: 16253912
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  • 14. Postmortem molecular analysis of KCNQ1 and SCN5A genes in sudden unexplained death in young Australians.
    Doolan A, Langlois N, Chiu C, Ingles J, Lind JM, Semsarian C.
    Int J Cardiol; 2008 Jun 23; 127(1):138-41. PubMed ID: 17544529
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  • 15. Mutation site-specific differences in arrhythmic risk and sensitivity to sympathetic stimulation in the LQT1 form of congenital long QT syndrome: multicenter study in Japan.
    Shimizu W, Horie M, Ohno S, Takenaka K, Yamaguchi M, Shimizu M, Washizuka T, Aizawa Y, Nakamura K, Ohe T, Aiba T, Miyamoto Y, Yoshimasa Y, Towbin JA, Priori SG, Kamakura S.
    J Am Coll Cardiol; 2004 Jul 07; 44(1):117-25. PubMed ID: 15234419
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  • 16. Mutation detection in congenital long QT syndrome: cardiac channel gene screen using PCR, dHPLC, and direct DNA sequencing.
    Tester DJ, Will ML, Ackerman MJ.
    Methods Mol Med; 2006 Jul 07; 128():181-207. PubMed ID: 17071997
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  • 18. Can a message from the dead save lives?
    Schwartz PJ, Crotti L.
    J Am Coll Cardiol; 2007 Jan 16; 49(2):247-9. PubMed ID: 17222737
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  • 19. Cardiac channelopathy testing in 274 ethnically diverse sudden unexplained deaths.
    Wang D, Shah KR, Um SY, Eng LS, Zhou B, Lin Y, Mitchell AA, Nicaj L, Prinz M, McDonald TV, Sampson BA, Tang Y.
    Forensic Sci Int; 2014 Apr 16; 237():90-9. PubMed ID: 24631775
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