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PUBMED FOR HANDHELDS

Journal Abstract Search

504 related items for PubMed ID: 19083750

  • 21.
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  • 22. [Relationship between congenital long QT syndrome and Brugada syndrome gene mutation].
    Du R, Ren FX, Yang JG, Yuan GH, Zhang SY, Kang CL, Li W, Gui L, Li J.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2005 Jun; 27(3):289-94. PubMed ID: 16038262
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  • 25. Look beyond the hERG mutation: a neutral SCN5A variant may turn lidocaine into a threat.
    Lindegger N, Mongillo M.
    Heart Rhythm; 2008 Nov; 5(11):1575-6. PubMed ID: 18984535
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  • 30. 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
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  • 31. 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; 9(3):259-65. PubMed ID: 27114410
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  • 32. Prospective, population-based long QT molecular autopsy study of postmortem negative sudden death in 1 to 40 year olds.
    Skinner JR, Crawford J, Smith W, Aitken A, Heaven D, Evans CA, Hayes I, Neas KR, Stables S, Koelmeyer T, Denmark L, Vuletic J, Maxwell F, White K, Yang T, Roden DM, Leren TP, Shelling A, Love DR, Cardiac Inherited Disease Group New Zealand.
    Heart Rhythm; 2011 Mar; 8(3):412-9. PubMed ID: 21070882
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  • 34. [Gene mutation analysis of a Chinese family of congenital long Q-T syndrome type three].
    Shi RM, Ma AQ, Zhang YM, Yang C, Huang C, Zhou XH, Liu XH.
    Zhonghua Er Ke Za Zhi; 2009 Dec; 47(12):926-30. PubMed ID: 20193146
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  • 36. Long QT molecular autopsy in sudden infant death syndrome.
    Glengarry JM, Crawford J, Morrow PL, Stables SR, Love DR, Skinner JR.
    Arch Dis Child; 2014 Jul; 99(7):635-40. PubMed ID: 24596401
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  • 37. Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.
    Kapplinger JD, Tester DJ, Salisbury BA, Carr JL, Harris-Kerr C, Pollevick GD, Wilde AA, Ackerman MJ.
    Heart Rhythm; 2009 Sep; 6(9):1297-303. PubMed ID: 19716085
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  • 38. Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current.
    Cheng J, Van Norstrand DW, Medeiros-Domingo A, Valdivia C, Tan BH, Ye B, Kroboth S, Vatta M, Tester DJ, January CT, Makielski JC, Ackerman MJ.
    Circ Arrhythm Electrophysiol; 2009 Dec; 2(6):667-76. PubMed ID: 20009079
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  • 39. Latent genetic backgrounds and molecular pathogenesis in drug-induced long-QT syndrome.
    Itoh H, Sakaguchi T, Ding WG, Watanabe E, Watanabe I, Nishio Y, Makiyama T, Ohno S, Akao M, Higashi Y, Zenda N, Kubota T, Mori C, Okajima K, Haruna T, Miyamoto A, Kawamura M, Ishida K, Nagaoka I, Oka Y, Nakazawa Y, Yao T, Jo H, Sugimoto Y, Ashihara T, Hayashi H, Ito M, Imoto K, Matsuura H, Horie M.
    Circ Arrhythm Electrophysiol; 2009 Oct; 2(5):511-23. PubMed ID: 19843919
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