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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

159 related items for PubMed ID: 22966897

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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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  • 3. Mutation Analysis of KCNQ1, KCNH2 and SCN5A Genes in Taiwanese Long QT Syndrome Patients.
    Chang YS, Yang YW, Lin YN, Lin KH, Chang KC, Chang JG.
    Int Heart J; 2015 Oct; 56(4):450-3. PubMed ID: 26118593
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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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  • 11. The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
    Vincent GM.
    Annu Rev Med; 1998 Oct; 49():263-74. PubMed ID: 9509262
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  • 12. Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention.
    Goldman AM, Behr ER, Semsarian C, Bagnall RD, Sisodiya S, Cooper PN.
    Epilepsia; 2016 Jan; 57 Suppl 1(Suppl 1):17-25. PubMed ID: 26749013
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  • 14. Genetics of long QT syndrome.
    Tester DJ, Ackerman MJ.
    Methodist Debakey Cardiovasc J; 2014 Jan; 10(1):29-33. PubMed ID: 24932360
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  • 15. Mutation analysis for the detection of long QT-syndrome (LQTS) associated SNPs.
    J E, T D, M S, M KN, J D, M NW.
    Int J Legal Med; 2017 Mar; 131(2):333-338. PubMed ID: 27613431
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  • 16. Arrhythmia phenotype during fetal life suggests long-QT syndrome genotype: risk stratification of perinatal long-QT syndrome.
    Cuneo BF, Etheridge SP, Horigome H, Sallee D, Moon-Grady A, Weng HY, Ackerman MJ, Benson DW.
    Circ Arrhythm Electrophysiol; 2013 Oct; 6(5):946-51. PubMed ID: 23995044
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  • 19. Clinical characteristics of patients with congenital long QT syndrome and bigenic mutations.
    Jimmy JJ, Chen CY, Yeh HM, Chiu WY, Yu CC, Liu YB, Tsai CT, Lo LW, Yeh SF, Lai LP.
    Chin Med J (Engl); 2014 Oct; 127(8):1482-6. PubMed ID: 24762593
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