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Page 1
Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study.
Behr ER, Savio-Galimberti E, Barc J, Holst AG, Petropoulou E, Prins BP, Jabbari J, Torchio M, Berthet M, Mizusawa Y, Yang T, Nannenberg EA, Dagradi F, Weeke P, Bastiaenan R, Ackerman MJ, Haunso S, Leenhardt A, Kääb S, Probst V, Redon R, Sharma S, Wilde A, Tfelt-Hansen J, Schwartz P, Roden DM, Bezzina CR, Olesen M, Darbar D, Guicheney P, Crotti L; UK10K Consortium; Jamshidi Y. Behr ER, et al. Among authors: crotti l. Cardiovasc Res. 2015 Jun 1;106(3):520-9. doi: 10.1093/cvr/cvv042. Epub 2015 Feb 17. Cardiovasc Res. 2015. PMID: 25691538 Free PMC article.
KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome.
Crotti L, Lundquist AL, Insolia R, Pedrazzini M, Ferrandi C, De Ferrari GM, Vicentini A, Yang P, Roden DM, George AL Jr, Schwartz PJ. Crotti L, et al. Circulation. 2005 Aug 30;112(9):1251-8. doi: 10.1161/CIRCULATIONAHA.105.549071. Epub 2005 Aug 22. Circulation. 2005. PMID: 16116052
Prevalence of long-QT syndrome gene variants in sudden infant death syndrome.
Arnestad M, Crotti L, Rognum TO, Insolia R, Pedrazzini M, Ferrandi C, Vege A, Wang DW, Rhodes TE, George AL Jr, Schwartz PJ. Arnestad M, et al. Among authors: crotti l. Circulation. 2007 Jan 23;115(3):361-7. doi: 10.1161/CIRCULATIONAHA.106.658021. Epub 2007 Jan 8. Circulation. 2007. PMID: 17210839
Cardiac sodium channel dysfunction in sudden infant death syndrome.
Wang DW, Desai RR, Crotti L, Arnestad M, Insolia R, Pedrazzini M, Ferrandi C, Vege A, Rognum T, Schwartz PJ, George AL Jr. Wang DW, et al. Among authors: crotti l. Circulation. 2007 Jan 23;115(3):368-76. doi: 10.1161/CIRCULATIONAHA.106.646513. Epub 2007 Jan 8. Circulation. 2007. PMID: 17210841
Can a message from the dead save lives?
Schwartz PJ, Crotti L. Schwartz PJ, et al. Among authors: crotti l. J Am Coll Cardiol. 2007 Jan 16;49(2):247-9. doi: 10.1016/j.jacc.2006.10.009. Epub 2006 Dec 29. J Am Coll Cardiol. 2007. PMID: 17222737 Free article. No abstract available.
The common long-QT syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification.
Crotti L, Spazzolini C, Schwartz PJ, Shimizu W, Denjoy I, Schulze-Bahr E, Zaklyazminskaya EV, Swan H, Ackerman MJ, Moss AJ, Wilde AA, Horie M, Brink PA, Insolia R, De Ferrari GM, Crimi G. Crotti L, et al. Circulation. 2007 Nov 20;116(21):2366-75. doi: 10.1161/CIRCULATIONAHA.107.726950. Epub 2007 Nov 5. Circulation. 2007. PMID: 17984373
Cardiac potassium channel dysfunction in sudden infant death syndrome.
Rhodes TE, Abraham RL, Welch RC, Vanoye CG, Crotti L, Arnestad M, Insolia R, Pedrazzini M, Ferrandi C, Vege A, Rognum T, Roden DM, Schwartz PJ, George AL Jr. Rhodes TE, et al. Among authors: crotti l. J Mol Cell Cardiol. 2008 Mar;44(3):571-81. doi: 10.1016/j.yjmcc.2007.11.015. Epub 2007 Dec 7. J Mol Cell Cardiol. 2008. PMID: 18222468 Free PMC article.
Neural control of heart rate is an arrhythmia risk modifier in long QT syndrome.
Schwartz PJ, Vanoli E, Crotti L, Spazzolini C, Ferrandi C, Goosen A, Hedley P, Heradien M, Bacchini S, Turco A, La Rovere MT, Bartoli A, George AL Jr, Brink PA. Schwartz PJ, et al. Among authors: crotti l. J Am Coll Cardiol. 2008 Mar 4;51(9):920-9. doi: 10.1016/j.jacc.2007.09.069. J Am Coll Cardiol. 2008. PMID: 18308161 Free article.
235 results