Vatta M - Search Results

1

Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3.

Cronk LB, Ye B, Kaku T, Tester DJ, Vatta M, Makielski JC, Ackerman MJ. Cronk LB, et al. Among authors: vatta m. Heart Rhythm. 2007 Feb;4(2):161-6. doi: 10.1016/j.hrthm.2006.11.030. Epub 2006 Dec 6. Heart Rhythm. 2007. PMID: 17275750 Free PMC article.

2

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.

3

Genotype-phenotype relationships involving hypertrophic cardiomyopathy-associated mutations in titin, muscle LIM protein, and telethonin.

Bos JM, Poley RN, Ny M, Tester DJ, Xu X, Vatta M, Towbin JA, Gersh BJ, Ommen SR, Ackerman MJ. Bos JM, et al. Among authors: vatta m. Mol Genet Metab. 2006 May;88(1):78-85. doi: 10.1016/j.ymgme.2005.10.008. Epub 2005 Dec 13. Mol Genet Metab. 2006. PMID: 16352453 Free PMC article.

4

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

5

Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current.

Cheng J, Van Norstrand DW, Medeiros-Domingo A, Valdivia C, Tan BH, Ye B, Kroboth S, Vatta M, Tester DJ, January CT, Makielski JC, Ackerman MJ. Cheng J, et al. Among authors: vatta m. Circ Arrhythm Electrophysiol. 2009 Dec;2(6):667-76. doi: 10.1161/CIRCEP.109.891440. Circ Arrhythm Electrophysiol. 2009. PMID: 20009079 Free PMC article.

6

Genetics of heart failure and sudden death.

Vatta M, Ackerman MJ. Vatta M, et al. Heart Fail Clin. 2010 Oct;6(4):507-14, ix. doi: 10.1016/j.hfc.2010.05.008. Heart Fail Clin. 2010. PMID: 20869650 Review.

7

Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry.

Crotti L, Spazzolini C, Tester DJ, Ghidoni A, Baruteau AE, Beckmann BM, Behr ER, Bennett JS, Bezzina CR, Bhuiyan ZA, Celiker A, Cerrone M, Dagradi F, De Ferrari GM, Etheridge SP, Fatah M, Garcia-Pavia P, Al-Ghamdi S, Hamilton RM, Al-Hassnan ZN, Horie M, Jimenez-Jaimez J, Kanter RJ, Kaski JP, Kotta MC, Lahrouchi N, Makita N, Norrish G, Odland HH, Ohno S, Papagiannis J, Parati G, Sekarski N, Tveten K, Vatta M, Webster G, Wilde AAM, Wojciak J, George AL, Ackerman MJ, Schwartz PJ. Crotti L, et al. Among authors: vatta m. Eur Heart J. 2019 Sep 14;40(35):2964-2975. doi: 10.1093/eurheartj/ehz311. Eur Heart J. 2019. PMID: 31170290 Free PMC article.

8

Echocardiographic-determined septal morphology in Z-disc hypertrophic cardiomyopathy.

Theis JL, Bos JM, Bartleson VB, Will ML, Binder J, Vatta M, Towbin JA, Gersh BJ, Ommen SR, Ackerman MJ. Theis JL, et al. Among authors: vatta m. Biochem Biophys Res Commun. 2006 Dec 29;351(4):896-902. doi: 10.1016/j.bbrc.2006.10.119. Epub 2006 Nov 9. Biochem Biophys Res Commun. 2006. PMID: 17097056

9

Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex.

Ueda K, Valdivia C, Medeiros-Domingo A, Tester DJ, Vatta M, Farrugia G, Ackerman MJ, Makielski JC. Ueda K, et al. Among authors: vatta m. Proc Natl Acad Sci U S A. 2008 Jul 8;105(27):9355-60. doi: 10.1073/pnas.0801294105. Epub 2008 Jun 30. Proc Natl Acad Sci U S A. 2008. PMID: 18591664 Free PMC article.

10

alpha-1-syntrophin mutation and the long-QT syndrome: a disease of sodium channel disruption.

Wu G, Ai T, Kim JJ, Mohapatra B, Xi Y, Li Z, Abbasi S, Purevjav E, Samani K, Ackerman MJ, Qi M, Moss AJ, Shimizu W, Towbin JA, Cheng J, Vatta M. Wu G, et al. Among authors: vatta m. Circ Arrhythm Electrophysiol. 2008 Aug;1(3):193-201. doi: 10.1161/CIRCEP.108.769224. Circ Arrhythm Electrophysiol. 2008. PMID: 19684871 Free PMC article.

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