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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

504 related items for PubMed ID: 19083750

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  • 2. 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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  • 4. Molecular biology and cellular mechanisms of Brugada and long QT syndromes in infants and young children.
    Antzelevitch C.
    J Electrocardiol; 2001 Oct; 34 Suppl():177-81. PubMed ID: 11781953
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  • 6. 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; 254():5-11. PubMed ID: 26164358
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  • 13. 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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  • 15. Post-mortem review and genetic analysis of sudden unexpected death in epilepsy (SUDEP) cases.
    Tu E, Bagnall RD, Duflou J, Semsarian C.
    Brain Pathol; 2011 Mar; 21(2):201-8. PubMed ID: 20875080
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