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Phenotypic characterization of a large European family with Brugada syndrome displaying a sudden unexpected death syndrome mutation in SCN5A:
Hong K, Berruezo-Sanchez A, Poungvarin N, Oliva A, Vatta M, Brugada J, Brugada P, Towbin JA, Dumaine R, Piñero-Galvez C, Antzelevitch C, Brugada R. Hong K, et al. Among authors: brugada r, brugada p, brugada j. J Cardiovasc Electrophysiol. 2004 Jan;15(1):64-9. doi: 10.1046/j.1540-8167.2004.03341.x. J Cardiovasc Electrophysiol. 2004. PMID: 15028074
Cryptic 5' splice site activation in SCN5A associated with Brugada syndrome.
Hong K, Guerchicoff A, Pollevick GD, Oliva A, Dumaine R, de Zutter M, Burashnikov E, Wu YS, Brugada J, Brugada P, Brugada R. Hong K, et al. Among authors: brugada r, brugada p, brugada j. J Mol Cell Cardiol. 2005 Apr;38(4):555-60. doi: 10.1016/j.yjmcc.2004.10.015. Epub 2004 Dec 9. J Mol Cell Cardiol. 2005. PMID: 15808832
De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero.
Hong K, Piper DR, Diaz-Valdecantos A, Brugada J, Oliva A, Burashnikov E, Santos-de-Soto J, Grueso-Montero J, Diaz-Enfante E, Brugada P, Sachse F, Sanguinetti MC, Brugada R. Hong K, et al. Among authors: brugada r, brugada p, brugada j. Cardiovasc Res. 2005 Dec 1;68(3):433-40. doi: 10.1016/j.cardiores.2005.06.023. Epub 2005 Aug 18. Cardiovasc Res. 2005. PMID: 16109388
SCN5A mutation associated with acute myocardial infarction.
Oliva A, Hu D, Viskin S, Carrier T, Cordeiro JM, Barajas-Martinez H, Wu Y, Burashnikov E, Brugada R, Rosso R, Guerchicoff A, Pollevick G, Pascali VL, Antzelevitch C. Oliva A, et al. Among authors: brugada r. Leg Med (Tokyo). 2009 Apr;11 Suppl 1(Suppl 1):S206-9. doi: 10.1016/j.legalmed.2009.02.044. Epub 2009 Apr 2. Leg Med (Tokyo). 2009. PMID: 19345130 Free PMC article.
404 results