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Journal Abstract Search

504 related items for PubMed ID: 19083750

  • 41. Mutations in the HERG K+-ion channel: a novel link between long QT syndrome and sudden infant death syndrome.
    Christiansen M, Tønder N, Larsen LA, Andersen PS, Simonsen H, Oyen N, Kanters JK, Jacobsen JR, Fosdal I, Wettrell G, Kjeldsen K.
    Am J Cardiol; 2005 Feb 01; 95(3):433-4. PubMed ID: 15670565
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  • 45. A sodium channel pore mutation causing Brugada syndrome.
    Pfahnl AE, Viswanathan PC, Weiss R, Shang LL, Sanyal S, Shusterman V, Kornblit C, London B, Dudley SC.
    Heart Rhythm; 2007 Jan 01; 4(1):46-53. PubMed ID: 17198989
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  • 46. Molecular autopsy for sudden unexplained death? Time to discuss pros and cons.
    Mazzanti A, Priori SG.
    J Cardiovasc Electrophysiol; 2012 Oct 01; 23(10):1099-102. PubMed ID: 22966897
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  • 48. Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patients.
    Fodstad H, Bendahhou S, Rougier JS, Laitinen-Forsblom PJ, Barhanin J, Abriel H, Schild L, Kontula K, Swan H.
    Ann Med; 2006 Oct 01; 38(4):294-304. PubMed ID: 16754261
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  • 49. Sudden infant death syndrome: how significant are the cardiac channelopathies?
    Tester DJ, Ackerman MJ.
    Cardiovasc Res; 2005 Aug 15; 67(3):388-96. PubMed ID: 15913580
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  • 52. 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 15; 20(6):475-6. PubMed ID: 12442276
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  • 55. An autopsy case of sudden unexpected nocturnal death syndrome with R1193Q polymorphism in the SCN5A gene.
    Matsusue A, Kashiwagi M, Hara K, Waters B, Sugimura T, Kubo S.
    Leg Med (Tokyo); 2012 Nov 15; 14(6):317-9. PubMed ID: 22682427
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  • 56. Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants.
    Kapa S, Tester DJ, Salisbury BA, Harris-Kerr C, Pungliya MS, Alders M, Wilde AA, Ackerman MJ.
    Circulation; 2009 Nov 03; 120(18):1752-60. PubMed ID: 19841300
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  • 57. Posthumous diagnosis of long QT syndrome from neonatal screening cards.
    Gladding PA, Evans CA, Crawford J, Chung SK, Vaughan A, Webster D, Neas K, Love DR, Rees MI, Shelling AN, Skinner JR.
    Heart Rhythm; 2010 Apr 03; 7(4):481-6. PubMed ID: 20167303
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  • 58. The implications of genetic mutations in the sodium channel gene (SCN5A).
    Moric E, Herbert E, Trusz-Gluza M, Filipecki A, Mazurek U, Wilczok T.
    Europace; 2003 Oct 03; 5(4):325-34. PubMed ID: 14753626
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  • 59. Congenital long-QT syndrome caused by a novel mutation in a conserved acidic domain of the cardiac Na+ channel.
    Wei J, Wang DW, Alings M, Fish F, Wathen M, Roden DM, George AL.
    Circulation; 1999 Jun 22; 99(24):3165-71. PubMed ID: 10377081
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  • 60. 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 22; 131(2):333-338. PubMed ID: 27613431
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