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Journal Abstract Search

209 related items for PubMed ID: 29214556

  • 1. Influence of genetic modifiers on sudden cardiac death cases.
    Jenewein T, Neumann T, Erkapic D, Kuniss M, Verhoff MA, Thiel G, Kauferstein S.
    Int J Legal Med; 2018 Mar; 132(2):379-385. PubMed ID: 29214556
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Identification novel LQT syndrome-associated variants in Polish population and genotype-phenotype correlations in eight families.
    Szperl M, Kozicka U, Kosiec A, Kukla P, Roszczynko M, Biernacka EK.
    J Appl Genet; 2018 Nov; 59(4):463-469. PubMed ID: 30244407
    [Abstract] [Full Text] [Related]

  • 7. 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; 96(3):172-8. PubMed ID: 21308345
    [Abstract] [Full Text] [Related]

  • 8. Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases.
    Neubauer J, Haas C, Bartsch C, Medeiros-Domingo A, Berger W.
    Int J Legal Med; 2016 Jul; 130(4):1011-1021. PubMed ID: 26846766
    [Abstract] [Full Text] [Related]

  • 9. Postmortem Analysis of 4 Mutation Hotspots of KCNQ1, KCNH2, and SCN5A Genes in Sudden Unexplained Death in Southwest of China.
    Jia PL, Wang YB, Fu H, Huang WL, Zhong SR, Ma L, Li YH, Dong Y, Sun ZC, Yang L, Qu PF, Zhao S, Qu YQ, Xi YM, Wang SW, Tang X, Lei PP.
    Am J Forensic Med Pathol; 2018 Sep; 39(3):218-222. PubMed ID: 29851656
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. 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
    [Abstract] [Full Text] [Related]

  • 13. Whole exome sequencing in Brugada and long QT syndromes revealed novel rare and potential pathogenic mutations related to the dysfunction of the cardiac sodium channel.
    Chen J, Li H, Guo S, Yang Z, Sun S, Zeng J, Gou H, Chen Y, Wang F, Lin Y, Huang K, Yue H, Ma Y, Lin Y.
    Orphanet J Rare Dis; 2022 Oct 27; 17(1):394. PubMed ID: 36303204
    [Abstract] [Full Text] [Related]

  • 14. Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance.
    Barc J, Briec F, Schmitt S, Kyndt F, Le Cunff M, Baron E, Vieyres C, Sacher F, Redon R, Le Caignec C, Le Marec H, Probst V, Schott JJ.
    J Am Coll Cardiol; 2011 Jan 04; 57(1):40-7. PubMed ID: 21185499
    [Abstract] [Full Text] [Related]

  • 15. Whole-Exome Molecular Autopsy After Exertion-Related Sudden Unexplained Death in the Young.
    Anderson JH, Tester DJ, Will ML, Ackerman MJ.
    Circ Cardiovasc Genet; 2016 Jun 04; 9(3):259-65. PubMed ID: 27114410
    [Abstract] [Full Text] [Related]

  • 16. KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.
    Liu W, Yang J, Hu D, Kang C, Li C, Zhang S, Li P, Chen Z, Qin X, Ying K, Li Y, Li Y, Li Z, Cheng X, Li L, Qi Y, Chen S, Wang Q.
    Hum Mutat; 2002 Dec 04; 20(6):475-6. PubMed ID: 12442276
    [Abstract] [Full Text] [Related]

  • 17. Cardiac sodium channel gene variants and sudden cardiac death in women.
    Albert CM, Nam EG, Rimm EB, Jin HW, Hajjar RJ, Hunter DJ, MacRae CA, Ellinor PT.
    Circulation; 2008 Jan 01; 117(1):16-23. PubMed ID: 18071069
    [Abstract] [Full Text] [Related]

  • 18. The role of known variants of KCNQ1, KCNH2, KCNE1, SCN5A, and NOS1AP in water-related deaths.
    Tzimas I, Zingraf JC, Bajanowski T, Poetsch M.
    Int J Legal Med; 2016 Nov 01; 130(6):1575-1579. PubMed ID: 27460199
    [Abstract] [Full Text] [Related]

  • 19. Genetic Variants on SCN5A, KCNQ1, and KCNH2 in Patients with Ventricular Arrhythmias during Acute Myocardial Infarction in a Chinese Population.
    Wang F, Liu Y, Liao H, Xue Y, Zhan X, Fang X, Liang Y, Wei W, Rao F, Zhang Q, Deng H, Lin Y, Liu F, Lin W, Zhang B, Wu S.
    Cardiology; 2020 Nov 01; 145(1):38-45. PubMed ID: 31751991
    [Abstract] [Full Text] [Related]

  • 20. Long QT syndrome with mutations in three genes: A rare case.
    Fernandes M, Martins Ribeiro S, Sanfins V, Lourenço A.
    Rev Port Cardiol; 2015 May 01; 34(5):359.e1-5. PubMed ID: 25935074
    [Abstract] [Full Text] [Related]

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