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Journal Abstract Search

420 related items for PubMed ID: 11710892

  • 1. Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome.
    Ackerman MJ, Siu BL, Sturner WQ, Tester DJ, Valdivia CR, Makielski JC, Towbin JA.
    JAMA; 2001 Nov 14; 286(18):2264-9. PubMed ID: 11710892
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  • 2. 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 14; 1(2):170-4. PubMed ID: 19083750
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  • 3. Sudden infant death syndrome-associated mutations in the sodium channel beta subunits.
    Tan BH, Pundi KN, Van Norstrand DW, Valdivia CR, Tester DJ, Medeiros-Domingo A, Makielski JC, Ackerman MJ.
    Heart Rhythm; 2010 Jun 14; 7(6):771-8. PubMed ID: 20226894
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  • 4. Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3.
    Cronk LB, Ye B, Kaku T, Tester DJ, Vatta M, Makielski JC, Ackerman MJ.
    Heart Rhythm; 2007 Feb 14; 4(2):161-6. PubMed ID: 17275750
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  • 6. De novo mutation in the SCN5A gene associated with early onset of sudden infant death.
    Wedekind H, Smits JP, Schulze-Bahr E, Arnold R, Veldkamp MW, Bajanowski T, Borggrefe M, Brinkmann B, Warnecke I, Funke H, Bhuiyan ZA, Wilde AA, Breithardt G, Haverkamp W.
    Circulation; 2001 Sep 04; 104(10):1158-64. PubMed ID: 11535573
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  • 7. 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 04; 5(4):325-34. PubMed ID: 14753626
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  • 8. A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y.
    Plant LD, Bowers PN, Liu Q, Morgan T, Zhang T, State MW, Chen W, Kittles RA, Goldstein SA.
    J Clin Invest; 2006 Feb 04; 116(2):430-5. PubMed ID: 16453024
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  • 10. A novel SCN5A arrhythmia mutation, M1766L, with expression defect rescued by mexiletine.
    Valdivia CR, Ackerman MJ, Tester DJ, Wada T, McCormack J, Ye B, Makielski JC.
    Cardiovasc Res; 2002 Aug 01; 55(2):279-89. PubMed ID: 12123767
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  • 11. Cardiac ion channel gene mutations in sudden infant death syndrome.
    Otagiri T, Kijima K, Osawa M, Ishii K, Makita N, Matoba R, Umetsu K, Hayasaka K.
    Pediatr Res; 2008 Nov 01; 64(5):482-7. PubMed ID: 18596570
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  • 12. Overrepresentation of the proarrhythmic, sudden death predisposing sodium channel polymorphism S1103Y in a population-based cohort of African-American sudden infant death syndrome.
    Van Norstrand DW, Tester DJ, Ackerman MJ.
    Heart Rhythm; 2008 May 01; 5(5):712-5. PubMed ID: 18452875
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  • 13. A mechanism for sudden infant death syndrome (SIDS): stress-induced leak via ryanodine receptors.
    Tester DJ, Dura M, Carturan E, Reiken S, Wronska A, Marks AR, Ackerman MJ.
    Heart Rhythm; 2007 Jun 01; 4(6):733-9. PubMed ID: 17556193
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  • 19. Biophysical characterization of a new SCN5A mutation S1333Y in a SIDS infant linked to long QT syndrome.
    Huang H, Millat G, Rodriguez-Lafrasse C, Rousson R, Kugener B, Chevalier P, Chahine M.
    FEBS Lett; 2009 Mar 04; 583(5):890-6. PubMed ID: 19302788
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