Crotti L - Search Results

1

Filtering approach based on empirical mode decomposition improves the assessment of short scale complexity in long QT syndrome type 1 population.

Bari V, Marchi A, Girardengo G, George AL Jr, Brink PA, Cerutti S, Crotti L, Schwartz PJ, Porta A. Bari V, et al. Among authors: crotti l. Annu Int Conf IEEE Eng Med Biol Soc. 2014;2014:6671-4. doi: 10.1109/EMBC.2014.6945158. Annu Int Conf IEEE Eng Med Biol Soc. 2014. PMID: 25571526

2

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

3

Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder population.

Brink PA, Crotti L, Corfield V, Goosen A, Durrheim G, Hedley P, Heradien M, Geldenhuys G, Vanoli E, Bacchini S, Spazzolini C, Lundquist AL, Roden DM, George AL Jr, Schwartz PJ. Brink PA, et al. Among authors: crotti l. Circulation. 2005 Oct 25;112(17):2602-10. doi: 10.1161/CIRCULATIONAHA.105.572453. Circulation. 2005. PMID: 16246960

4

Does pregnancy increase cardiac risk for LQT1 patients with the KCNQ1-A341V mutation?

Heradien MJ, Goosen A, Crotti L, Durrheim G, Corfield V, Brink PA, Schwartz PJ. Heradien MJ, et al. Among authors: crotti l. J Am Coll Cardiol. 2006 Oct 3;48(7):1410-5. doi: 10.1016/j.jacc.2006.05.060. Epub 2006 Sep 14. J Am Coll Cardiol. 2006. PMID: 17010804 Free article.

5

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

6

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

7

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.

8

Cardiac arrhythmias of genetic origin are important contributors to sudden infant death syndrome.

Schwartz PJ, Crotti L. Schwartz PJ, et al. Among authors: crotti l. Heart Rhythm. 2007 Jun;4(6):740-2. doi: 10.1016/j.hrthm.2007.03.035. Epub 2007 Apr 6. Heart Rhythm. 2007. PMID: 17556194 No abstract available.

9

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

10

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.

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