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440 results

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Page 1
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: antzelevitch c. 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.
Dual variation in SCN5A and CACNB2b underlies the development of cardiac conduction disease without Brugada syndrome.
Hu D, Barajas-Martinez H, Nesterenko VV, Pfeiffer R, Guerchicoff A, Cordeiro JM, Curtis AB, Pollevick GD, Wu Y, Burashnikov E, Antzelevitch C. Hu D, et al. Among authors: antzelevitch c. Pacing Clin Electrophysiol. 2010 Mar;33(3):274-85. doi: 10.1111/j.1540-8159.2009.02642.x. Epub 2009 Dec 16. Pacing Clin Electrophysiol. 2010. PMID: 20025708 Free PMC article.
A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype.
Hu D, Barajas-Martinez H, Burashnikov E, Springer M, Wu Y, Varro A, Pfeiffer R, Koopmann TT, Cordeiro JM, Guerchicoff A, Pollevick GD, Antzelevitch C. Hu D, et al. Among authors: antzelevitch c. Circ Cardiovasc Genet. 2009 Jun;2(3):270-8. doi: 10.1161/CIRCGENETICS.108.829192. Epub 2009 Apr 21. Circ Cardiovasc Genet. 2009. PMID: 20031595 Free PMC article.
An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing.
Kapplinger JD, Tester DJ, Alders M, Benito B, Berthet M, Brugada J, Brugada P, Fressart V, Guerchicoff A, Harris-Kerr C, Kamakura S, Kyndt F, Koopmann TT, Miyamoto Y, Pfeiffer R, Pollevick GD, Probst V, Zumhagen S, Vatta M, Towbin JA, Shimizu W, Schulze-Bahr E, Antzelevitch C, Salisbury BA, Guicheney P, Wilde AA, Brugada R, Schott JJ, Ackerman MJ. Kapplinger JD, et al. Among authors: antzelevitch c. Heart Rhythm. 2010 Jan;7(1):33-46. doi: 10.1016/j.hrthm.2009.09.069. Epub 2009 Oct 8. Heart Rhythm. 2010. PMID: 20129283 Free PMC article.
Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death.
Burashnikov E, Pfeiffer R, Barajas-Martinez H, Delpón E, Hu D, Desai M, Borggrefe M, Häissaguerre M, Kanter R, Pollevick GD, Guerchicoff A, Laiño R, Marieb M, Nademanee K, Nam GB, Robles R, Schimpf R, Stapleton DD, Viskin S, Winters S, Wolpert C, Zimmern S, Veltmann C, Antzelevitch C. Burashnikov E, et al. Among authors: antzelevitch c. Heart Rhythm. 2010 Dec;7(12):1872-82. doi: 10.1016/j.hrthm.2010.08.026. Epub 2010 Oct 14. Heart Rhythm. 2010. PMID: 20817017 Free PMC article.
Sudden death associated with short-QT syndrome linked to mutations in HERG.
Brugada R, Hong K, Dumaine R, Cordeiro J, Gaita F, Borggrefe M, Menendez TM, Brugada J, Pollevick GD, Wolpert C, Burashnikov E, Matsuo K, Wu YS, Guerchicoff A, Bianchi F, Giustetto C, Schimpf R, Brugada P, Antzelevitch C. Brugada R, et al. Among authors: antzelevitch c. Circulation. 2004 Jan 6;109(1):30-5. doi: 10.1161/01.CIR.0000109482.92774.3A. Epub 2003 Dec 15. Circulation. 2004. PMID: 14676148
Electrophysiologic properties and antiarrhythmic actions of a novel antianginal agent.
Antzelevitch C, Belardinelli L, Wu L, Fraser H, Zygmunt AC, Burashnikov A, Di Diego JM, Fish JM, Cordeiro JM, Goodrow RJ Jr, Scornik F, Perez G. Antzelevitch C, et al. J Cardiovasc Pharmacol Ther. 2004 Sep;9 Suppl 1:S65-83. doi: 10.1177/107424840400900106. J Cardiovasc Pharmacol Ther. 2004. PMID: 15378132 Review.
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: antzelevitch c. 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.
Brugada syndrome: 12 years of progression.
Hong K, Antzelevitch C, Brugada P, Brugada J, Ohe T, Brugada R. Hong K, et al. Among authors: antzelevitch c. Acta Med Okayama. 2004 Dec;58(6):255-61. doi: 10.18926/AMO/32094. Acta Med Okayama. 2004. PMID: 15762293 Free article. Review.
440 results