Schwartz PJ - Search Results

1

Mutation analysis of the phospholamban gene in 315 South Africans with dilated, hypertrophic, peripartum and arrhythmogenic right ventricular cardiomyopathies.

Fish M, Shaboodien G, Kraus S, Sliwa K, Seidman CE, Burke MA, Crotti L, Schwartz PJ, Mayosi BM. Fish M, et al. Among authors: schwartz pj. Sci Rep. 2016 Feb 26;6:22235. doi: 10.1038/srep22235. Sci Rep. 2016. PMID: 26917049 Free PMC article.

2

The elusive link between LQT3 and Brugada syndrome: the role of flecainide challenge.

Priori SG, Napolitano C, Schwartz PJ, Bloise R, Crotti L, Ronchetti E. Priori SG, et al. Among authors: schwartz pj. Circulation. 2000 Aug 29;102(9):945-7. doi: 10.1161/01.cir.102.9.945. Circulation. 2000. PMID: 10961955 Clinical Trial.

3

Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families.

Priori SG, Napolitano C, Gasparini M, Pappone C, Della Bella P, Brignole M, Giordano U, Giovannini T, Menozzi C, Bloise R, Crotti L, Terreni L, Schwartz PJ. Priori SG, et al. Among authors: schwartz pj. Circulation. 2000 Nov 14;102(20):2509-15. doi: 10.1161/01.cir.102.20.2509. Circulation. 2000. PMID: 11076825 Clinical Trial.

4

[Long QT syndrome and Brugada syndrome: 2 aspects of the same disease?].

Cerrone M, Crotti L, Faggiano G, De Michelis V, Napolitano C, Schwartz PJ, Priori SG. Cerrone M, et al. Among authors: schwartz pj. Ital Heart J Suppl. 2001 Mar;2(3):253-7. Ital Heart J Suppl. 2001. PMID: 11307783 Free article. Review. Italian.

5

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. Among authors: schwartz pj. Circulation. 2005 Aug 30;112(9):1251-8. doi: 10.1161/CIRCULATIONAHA.105.549071. Epub 2005 Aug 22. Circulation. 2005. PMID: 16116052

6

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: schwartz pj. Circulation. 2005 Oct 25;112(17):2602-10. doi: 10.1161/CIRCULATIONAHA.105.572453. Circulation. 2005. PMID: 16246960

7

The Jervell and Lange-Nielsen syndrome: natural history, molecular basis, and clinical outcome.

Schwartz PJ, Spazzolini C, Crotti L, Bathen J, Amlie JP, Timothy K, Shkolnikova M, Berul CI, Bitner-Glindzicz M, Toivonen L, Horie M, Schulze-Bahr E, Denjoy I. Schwartz PJ, et al. Circulation. 2006 Feb 14;113(6):783-90. doi: 10.1161/CIRCULATIONAHA.105.592899. Epub 2006 Feb 6. Circulation. 2006. PMID: 16461811

8

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: schwartz pj. 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.

9

Can a message from the dead save lives?

Schwartz PJ, Crotti L. Schwartz PJ, et al. 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.

10

Gene symbol: KCNH2.

Crotti L, Insolia R, Pedrazzini M, Andreoli C, Gabanti E, Moncalvo C, Crimi G, De Ferrari GM, Schwartz PJ. Crotti L, et al. Among authors: schwartz pj. Hum Genet. 2007 Feb;120(6):911. Hum Genet. 2007. PMID: 17438606 Free article. No abstract available.

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