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Journal Abstract Search

420 related items for PubMed ID: 11710892

  • 21.
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  • 22. Explaining sudden infant death with cardiac arrhythmias: Complete exon sequencing of nine cardiac arrhythmia genes in Dutch SIDS cases highlights new and known DNA variants.
    Liebrechts-Akkerman G, Liu F, van Marion R, Dinjens WNM, Kayser M.
    Forensic Sci Int Genet; 2020 May; 46():102266. PubMed ID: 32145446
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  • 23. Malignant perinatal variant of long-QT syndrome caused by a profoundly dysfunctional cardiac sodium channel.
    Wang DW, Crotti L, Shimizu W, Pedrazzini M, Cantu F, De Filippo P, Kishiki K, Miyazaki A, Ikeda T, Schwartz PJ, George AL.
    Circ Arrhythm Electrophysiol; 2008 Dec; 1(5):370-8. PubMed ID: 19808432
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  • 26. 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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  • 28. Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) mutations in sudden infant death syndrome.
    Van Norstrand DW, Valdivia CR, Tester DJ, Ueda K, London B, Makielski JC, Ackerman MJ.
    Circulation; 2007 Nov 13; 116(20):2253-9. PubMed ID: 17967976
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  • 29. 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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  • 30. Contribution of long-QT syndrome genetic variants in sudden infant death syndrome.
    Millat G, Kugener B, Chevalier P, Chahine M, Huang H, Malicier D, Rodriguez-Lafrasse C, Rousson R.
    Pediatr Cardiol; 2009 May 15; 30(4):502-9. PubMed ID: 19322600
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  • 31.
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  • 32. SCN4B-encoded sodium channel beta4 subunit in congenital long-QT syndrome.
    Medeiros-Domingo A, Kaku T, Tester DJ, Iturralde-Torres P, Itty A, Ye B, Valdivia C, Ueda K, Canizales-Quinteros S, Tusié-Luna MT, Makielski JC, Ackerman MJ.
    Circulation; 2007 Jul 10; 116(2):134-42. PubMed ID: 17592081
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  • 33. Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study.
    Wedekind H, Bajanowski T, Friederich P, Breithardt G, Wülfing T, Siebrands C, Engeland B, Mönnig G, Haverkamp W, Brinkmann B, Schulze-Bahr E.
    Int J Legal Med; 2006 May 10; 120(3):129-37. PubMed ID: 16012827
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  • 34. GPD1L links redox state to cardiac excitability by PKC-dependent phosphorylation of the sodium channel SCN5A.
    Valdivia CR, Ueda K, Ackerman MJ, Makielski JC.
    Am J Physiol Heart Circ Physiol; 2009 Oct 10; 297(4):H1446-52. PubMed ID: 19666841
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  • 35. 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 10; 4(10):1306-14. PubMed ID: 17905336
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  • 36. A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currents.
    Hu D, Barajas-Martínez H, Medeiros-Domingo A, Crotti L, Veltmann C, Schimpf R, Urrutia J, Alday A, Casis O, Pfeiffer R, Burashnikov E, Caceres G, Tester DJ, Wolpert C, Borggrefe M, Schwartz P, Ackerman MJ, Antzelevitch C.
    Heart Rhythm; 2012 May 10; 9(5):760-9. PubMed ID: 22155597
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  • 37. Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing.
    Ackerman MJ, Splawski I, Makielski JC, Tester DJ, Will ML, Timothy KW, Keating MT, Jones G, Chadha M, Burrow CR, Stephens JC, Xu C, Judson R, Curran ME.
    Heart Rhythm; 2004 Nov 10; 1(5):600-7. PubMed ID: 15851227
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  • 40. Genomic organization of the human SCN5A gene encoding the cardiac sodium channel.
    Wang Q, Li Z, Shen J, Keating MT.
    Genomics; 1996 May 15; 34(1):9-16. PubMed ID: 8661019
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