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Journal Abstract Search


389 related items for PubMed ID: 18252757

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  • 3. Characterization of a novel SCN5A mutation associated with Brugada syndrome reveals involvement of DIIIS4-S5 linker in slow inactivation.
    Casini S, Tan HL, Bhuiyan ZA, Bezzina CR, Barnett P, Cerbai E, Mugelli A, Wilde AA, Veldkamp MW.
    Cardiovasc Res; 2007 Dec 01; 76(3):418-29. PubMed ID: 17854786
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  • 6. The occurrence of Brugada syndrome and isolated cardiac conductive disease in the same family could be due to a single SCN5A mutation or to the accidental association of both diseases.
    Six I, Hermida JS, Huang H, Gouas L, Fressart V, Benammar N, Hainque B, Denjoy I, Chahine M, Guicheney P.
    Europace; 2008 Jan 01; 10(1):79-85. PubMed ID: 18156160
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  • 12. Pathophysiological mechanisms of Brugada syndrome: depolarization disorder, repolarization disorder, or more?
    Meregalli PG, Wilde AA, Tan HL.
    Cardiovasc Res; 2005 Aug 15; 67(3):367-78. PubMed ID: 15913579
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  • 19. Criteria to predict carriers of a novel SCN5A mutation in a large Portuguese family affected by the Brugada syndrome.
    Santos LF, Rodrigues B, Moreira D, Correia E, Nunes L, Costa A, Elvas L, Pereira T, Machado JC, Castedo S, Henriques C, Matos A, Santos JO.
    Europace; 2012 Jun 15; 14(6):882-8. PubMed ID: 22277643
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