Vatta M - Search Results

1

KCNE2 modulation of Kv4.3 current and its potential role in fatal rhythm disorders.

Wu J, Shimizu W, Ding WG, Ohno S, Toyoda F, Itoh H, Zang WJ, Miyamoto Y, Kamakura S, Matsuura H, Nademanee K, Brugada J, Brugada P, Brugada R, Vatta M, Towbin JA, Antzelevitch C, Horie M. Wu J, et al. Among authors: vatta m. Heart Rhythm. 2010;7(2):199-205. doi: 10.1016/j.hrthm.2009.10.012. Epub 2009 Oct 12. Heart Rhythm. 2010. PMID: 20042375 Free PMC article.

2

Mutations in KCNE1 in long QT syndrome (LQTS): insights into mechanism of LQTS and drug sensitivity?

Vatta M, Towbin JA. Vatta M, et al. Heart Rhythm. 2006 Sep;3(9):1041-2. doi: 10.1016/j.hrthm.2006.07.020. Epub 2006 Jul 21. Heart Rhythm. 2006. PMID: 16945798 No abstract available.

3

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: vatta m. 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.

4

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. Hum Mol Genet. 2002 Feb 1;11(3):337-45. doi: 10.1093/hmg/11.3.337. Hum Mol Genet. 2002. PMID: 11823453

5

A novel SCN5A mutation V1340I in Brugada syndrome augmenting arrhythmias during febrile illness.

Samani K, Wu G, Ai T, Shuraih M, Mathuria NS, Li Z, Sohma Y, Purevjav E, Xi Y, Towbin JA, Cheng J, Vatta M. Samani K, et al. Among authors: vatta m. Heart Rhythm. 2009 Sep;6(9):1318-26. doi: 10.1016/j.hrthm.2009.05.016. Epub 2009 May 18. Heart Rhythm. 2009. PMID: 19648062 Free PMC article.

6

Ionic mechanisms responsible for the electrocardiographic phenotype of the Brugada syndrome are temperature dependent.

Dumaine R, Towbin JA, Brugada P, Vatta M, Nesterenko DV, Nesterenko VV, Brugada J, Brugada R, Antzelevitch C. Dumaine R, et al. Among authors: vatta m. Circ Res. 1999 Oct 29;85(9):803-9. doi: 10.1161/01.res.85.9.803. Circ Res. 1999. PMID: 10532948

7

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. Mol Genet Metab. 2002 Apr;75(4):317-24. doi: 10.1016/S1096-7192(02)00006-9. Mol Genet Metab. 2002. PMID: 12051963

8

Myocardial infarction, viral infection, and the cytoskeleton final common pathways of a common disease?

Towbin JA, Vatta M. Towbin JA, et al. Among authors: vatta m. J Am Coll Cardiol. 2007 Dec 4;50(23):2215-7. doi: 10.1016/j.jacc.2007.08.034. Epub 2007 Nov 19. J Am Coll Cardiol. 2007. PMID: 18061068 Free article. No abstract available.

9

A nonsense SCN5A mutation associated with Brugada-type electrocardiogram and intraventricular conduction defects.

Samani K, Ai T, Towbin JA, Brugada R, Shuraih M, Xi Y, Wu G, Cheng J, Vatta M. Samani K, et al. Among authors: vatta m. Pacing Clin Electrophysiol. 2009 Sep;32(9):1231-6. doi: 10.1111/j.1540-8159.2009.02470.x. Pacing Clin Electrophysiol. 2009. PMID: 19719504 Free PMC article.

10

Arrhythmogenic right ventricular cardiomyopathy: a 'final common pathway' that defines clinical phenotype.

Vatta M, Marcus F, Towbin JA. Vatta M, et al. Eur Heart J. 2007 Mar;28(5):529-30. doi: 10.1093/eurheartj/ehl530. Epub 2007 Feb 15. Eur Heart J. 2007. PMID: 17303588 No abstract available.

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