Vatta M - Search Results

1

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

2

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

3

Genetics and cardiac arrhythmias.

Towbin JA, Vatta M, Li H, Bowles NE. Towbin JA, et al. Among authors: vatta m. Adv Pediatr. 2002;49:87-129. Adv Pediatr. 2002. PMID: 12214781 Review.

4

Genetics of brugada, long QT, and arrhythmogenic right ventricular dysplasia syndromes.

Towbin JA, Vatta M, Li H. Towbin JA, et al. Among authors: vatta m. J Electrocardiol. 2000;33 Suppl:11-22. doi: 10.1054/jelc.2000.20361. J Electrocardiol. 2000. PMID: 11265709 Review.

5

Mutations in the muscle LIM protein and alpha-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis.

Mohapatra B, Jimenez S, Lin JH, Bowles KR, Coveler KJ, Marx JG, Chrisco MA, Murphy RT, Lurie PR, Schwartz RJ, Elliott PM, Vatta M, McKenna W, Towbin JA, Bowles NE. Mohapatra B, et al. Among authors: vatta m. Mol Genet Metab. 2003 Sep-Oct;80(1-2):207-15. doi: 10.1016/s1096-7192(03)00142-2. Mol Genet Metab. 2003. PMID: 14567970

6

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: vatta m. J Cardiovasc Electrophysiol. 2004 Jan;15(1):64-9. doi: 10.1046/j.1540-8167.2004.03341.x. J Cardiovasc Electrophysiol. 2004. PMID: 15028074

7

Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome.

Vatta M, Ackerman MJ, Ye B, Makielski JC, Ughanze EE, Taylor EW, Tester DJ, Balijepalli RC, Foell JD, Li Z, Kamp TJ, Towbin JA. Vatta M, et al. Circulation. 2006 Nov 14;114(20):2104-12. doi: 10.1161/CIRCULATIONAHA.106.635268. Epub 2006 Oct 23. Circulation. 2006. PMID: 17060380

8

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: vatta m. 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

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

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

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