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The Brugada syndrome.
Escárcega RO, Jiménez-Hernández M, Garcia-Carrasco M, Perez-Alva JC, Brugada J. Escárcega RO, et al. Among authors: brugada j. Acta Cardiol. 2009 Dec;64(6):795-801. doi: 10.2143/AC.64.6.2044745. Acta Cardiol. 2009. PMID: 20128157 Review.
Novel mutations in domain I of SCN5A cause Brugada syndrome.
Vatta M, Dumaine R, Antzelevitch C, Brugada R, Li H, Bowles NE, Nademanee K, Brugada J, Brugada P, Towbin JA. Vatta M, et al. Among authors: brugada r, brugada p, brugada j. Mol Genet Metab. 2002 Apr;75(4):317-24. doi: 10.1016/S1096-7192(02)00006-9. Mol Genet Metab. 2002. PMID: 12051963
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
Brugada syndrome: 12 years of progression.
Hong K, Antzelevitch C, Brugada P, Brugada J, Ohe T, Brugada R. Hong K, et al. Among authors: brugada r, brugada p, brugada j. Acta Med Okayama. 2004 Dec;58(6):255-61. doi: 10.18926/AMO/32094. Acta Med Okayama. 2004. PMID: 15762293 Free article. Review.
Compound heterozygous mutations P336L and I1660V in the human cardiac sodium channel associated with the Brugada syndrome.
Cordeiro JM, Barajas-Martinez H, Hong K, Burashnikov E, Pfeiffer R, Orsino AM, Wu YS, Hu D, Brugada J, Brugada P, Antzelevitch C, Dumaine R, Brugada R. Cordeiro JM, et al. Among authors: brugada r, brugada p, brugada j. Circulation. 2006 Nov 7;114(19):2026-33. doi: 10.1161/CIRCULATIONAHA.106.627489. Epub 2006 Oct 30. Circulation. 2006. PMID: 17075016 Free PMC article.
Brugada syndrome.
Benito B, Brugada R, Brugada J, Brugada P. Benito B, et al. Among authors: brugada r, brugada p, brugada j. Prog Cardiovasc Dis. 2008 Jul-Aug;51(1):1-22. doi: 10.1016/j.pcad.2008.05.002. Prog Cardiovasc Dis. 2008. PMID: 18634914 Review.
Genetic modulation of brugada syndrome by a common polymorphism.
Lizotte E, Junttila MJ, Dube MP, Hong K, Benito B, DE Zutter M, Henkens S, Sarkozy A, Huikuri HV, Towbin J, Vatta M, Brugada P, Brugada J, Brugada R. Lizotte E, et al. Among authors: brugada r, brugada p, brugada j. J Cardiovasc Electrophysiol. 2009 Oct;20(10):1137-41. doi: 10.1111/j.1540-8167.2009.01508.x. Epub 2009 Jun 22. J Cardiovasc Electrophysiol. 2009. PMID: 19549036
BACKGROUND: Brugada syndrome predisposes some subjects to ventricular tachyarrhythmias and sudden cardiac death. ...We studied whether common variant H558R has any clinical implications in the phenotype of Brugada syndrome. METHODS: Our study population consisted of …
BACKGROUND: Brugada syndrome predisposes some subjects to ventricular tachyarrhythmias and sudden cardiac death. ...We studied whethe …
Brugada syndrome.
Benito B, Brugada J, Brugada R, Brugada P. Benito B, et al. Among authors: brugada r, brugada p, brugada j. Rev Esp Cardiol. 2009 Nov;62(11):1297-315. doi: 10.1016/s1885-5857(09)73357-2. Rev Esp Cardiol. 2009. PMID: 19889341 Free article. Review.
Sleep-disordered breathing in patients with the Brugada syndrome.
Macedo PG, Brugada J, Leinveber P, Benito B, Molina I, Sert-Kuniyoshi F, Adachi T, Bukartyk J, van der Walt C, Konecny T, Maharaj S, Kara T, Montserrat J, Somers V. Macedo PG, et al. Among authors: brugada j. Am J Cardiol. 2011 Mar 1;107(5):709-13. doi: 10.1016/j.amjcard.2010.10.046. Epub 2011 Jan 19. Am J Cardiol. 2011. PMID: 21247540 Free PMC article.
Risk stratification and treatment of brugada syndrome.
Arbelo E, Brugada J. Arbelo E, et al. Among authors: brugada j. Curr Cardiol Rep. 2014 Jul;16(7):508. doi: 10.1007/s11886-014-0508-1. Curr Cardiol Rep. 2014. PMID: 24893941 Review.
684 results