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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2005 | 1 |
2006 | 2 |
2007 | 1 |
2008 | 1 |
2009 | 1 |
2024 | 0 |
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SCN5A mutation associated with acute myocardial infarction.
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.
Lidocaine-induced Brugada syndrome phenotype linked to a novel double mutation in the cardiac sodium channel.
Barajas-Martínez HM, Hu D, Cordeiro JM, Wu Y, Kovacs RJ, Meltser H, Kui H, Elena B, Brugada R, Antzelevitch C, Dumaine R.
Barajas-Martínez HM, et al.
Circ Res. 2008 Aug 15;103(4):396-404. doi: 10.1161/CIRCRESAHA.108.172619. Epub 2008 Jul 3.
Circ Res. 2008.
PMID: 18599870
Free PMC article.
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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.
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.
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Genetic and biophysical basis for bupivacaine-induced ST segment elevation and VT/VF. Anesthesia unmasked Brugada syndrome.
Vernooy K, Sicouri S, Dumaine R, Hong K, Oliva A, Burashnikov E, Timmermans C, Delhaas T, Crijns HJ, Antzelevitch C, Rodriguez LM, Brugada R.
Vernooy K, et al.
Heart Rhythm. 2006 Sep;3(9):1074-8. doi: 10.1016/j.hrthm.2006.05.030. Epub 2006 Jul 7.
Heart Rhythm. 2006.
PMID: 16945804
Free PMC article.
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Electrocardiographic changes predicting sudden death in propofol-related infusion syndrome.
Vernooy K, Delhaas T, Cremer OL, Di Diego JM, Oliva A, Timmermans C, Volders PG, Prinzen FW, Crijns HJ, Antzelevitch C, Kalkman CJ, Rodriguez LM, Brugada R.
Vernooy K, et al.
Heart Rhythm. 2006 Feb;3(2):131-7. doi: 10.1016/j.hrthm.2005.11.005.
Heart Rhythm. 2006.
PMID: 16443524
Free PMC article.
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Short QT syndrome and atrial fibrillation caused by mutation in KCNH2.
Hong K, Bjerregaard P, Gussak I, Brugada R.
Hong K, et al.
J Cardiovasc Electrophysiol. 2005 Apr;16(4):394-6. doi: 10.1046/j.1540-8167.2005.40621.x.
J Cardiovasc Electrophysiol. 2005.
PMID: 15828882
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