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1,106 results

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Page 1
Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death.
Antzelevitch C, Pollevick GD, Cordeiro JM, Casis O, Sanguinetti MC, Aizawa Y, Guerchicoff A, Pfeiffer R, Oliva A, Wollnik B, Gelber P, Bonaros EP Jr, Burashnikov E, Wu Y, Sargent JD, Schickel S, Oberheiden R, Bhatia A, Hsu LF, Haïssaguerre M, Schimpf R, Borggrefe M, Wolpert C. Antzelevitch C, et al. Among authors: oliva a. Circulation. 2007 Jan 30;115(4):442-9. doi: 10.1161/CIRCULATIONAHA.106.668392. Epub 2007 Jan 15. Circulation. 2007. PMID: 17224476 Free PMC article.
Value of electrocardiographic parameters and ajmaline test in the diagnosis of Brugada syndrome caused by SCN5A mutations.
Hong K, Brugada J, Oliva A, Berruezo-Sanchez A, Potenza D, Pollevick GD, Guerchicoff A, Matsuo K, Burashnikov E, Dumaine R, Towbin JA, Nesterenko V, Brugada P, Antzelevitch C, Brugada R. Hong K, et al. Among authors: oliva a. Circulation. 2004 Nov 9;110(19):3023-7. doi: 10.1161/01.CIR.0000144299.17008.07. Epub 2004 Nov 1. Circulation. 2004. PMID: 15520322 Free PMC article.
Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction.
Hu D, Viskin S, Oliva A, Carrier T, Cordeiro JM, Barajas-Martinez H, Wu Y, Burashnikov E, Sicouri S, Brugada R, Rosso R, Guerchicoff A, Pollevick GD, Antzelevitch C. Hu D, et al. Among authors: oliva a. Heart Rhythm. 2007 Aug;4(8):1072-80. doi: 10.1016/j.hrthm.2007.03.040. Epub 2007 Apr 10. Heart Rhythm. 2007. PMID: 17675083 Free PMC article.
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: oliva a. 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: oliva a. 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
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: oliva a. J Cardiovasc Electrophysiol. 2004 Jan;15(1):64-9. doi: 10.1046/j.1540-8167.2004.03341.x. J Cardiovasc Electrophysiol. 2004. PMID: 15028074
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. 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.
1,106 results