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Page 1
Genetic analysis, in silico prediction, and family segregation in long QT syndrome.
Riuró H, Campuzano O, Berne P, Arbelo E, Iglesias A, Pérez-Serra A, Coll-Vidal M, Partemi S, Mademont-Soler I, Picó F, Allegue C, Oliva A, Gerstenfeld E, Sarquella-Brugada G, Castro-Urda V, Fernández-Lozano I, Mont L, Brugada J, Scornik FS, Brugada R. Riuró H, et al. Among authors: brugada r, brugada j. Eur J Hum Genet. 2015 Jan;23(1):79-85. doi: 10.1038/ejhg.2014.54. Epub 2014 Mar 26. Eur J Hum Genet. 2015. PMID: 24667783 Free PMC article.
Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome.
Vatta M, Dumaine R, Varghese G, Richard TA, Shimizu W, Aihara N, Nademanee K, Brugada R, Brugada J, Veerakul G, Li H, Bowles NE, Brugada P, Antzelevitch C, Towbin JA. Vatta M, et al. Among authors: brugada r, brugada p, brugada j. Hum Mol Genet. 2002 Feb 1;11(3):337-45. doi: 10.1093/hmg/11.3.337. Hum Mol Genet. 2002. PMID: 11823453
[Genetics and arrhythmias].
Brugada R, Brugada J, Brugada P. Brugada R, et al. Among authors: brugada p, brugada j. Rev Esp Cardiol. 2002 Apr;55(4):432-7. doi: 10.1016/s0300-8932(02)76621-9. Rev Esp Cardiol. 2002. PMID: 11975907 Free article. Review. Spanish.
The Brugada syndrome.
Brugada P, Brugada J, Brugada R. Brugada P, et al. Among authors: brugada r, brugada j. Card Electrophysiol Rev. 2002 Feb;6(1-2):45-8. doi: 10.1023/a:1017978903909. Card Electrophysiol Rev. 2002. PMID: 11984016 Review. No abstract available.
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
697 results