Schwartz PJ - Search Results

1

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: schwartz pj. Circulation. 2007 Jan 23;115(3):368-76. doi: 10.1161/CIRCULATIONAHA.106.646513. Epub 2007 Jan 8. Circulation. 2007. PMID: 17210841

2

ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome.

Moss AJ, Zareba W, Benhorin J, Locati EH, Hall WJ, Robinson JL, Schwartz PJ, Towbin JA, Vincent GM, Lehmann MH. Moss AJ, et al. Among authors: schwartz pj. Circulation. 1995 Nov 15;92(10):2929-34. doi: 10.1161/01.cir.92.10.2929. Circulation. 1995. PMID: 7586261

3

Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.

Schwartz PJ, Priori SG, Locati EH, Napolitano C, Cantù F, Towbin JA, Keating MT, Hammoude H, Brown AM, Chen LS, Colatsky TJ. Schwartz PJ, et al. Circulation. 1995 Dec 15;92(12):3381-6. doi: 10.1161/01.cir.92.12.3381. Circulation. 1995. PMID: 8521555

4

Multiple mechanisms of Na+ channel--linked long-QT syndrome.

Dumaine R, Wang Q, Keating MT, Hartmann HA, Schwartz PJ, Brown AM, Kirsch GE. Dumaine R, et al. Among authors: schwartz pj. Circ Res. 1996 May;78(5):916-24. doi: 10.1161/01.res.78.5.916. Circ Res. 1996. PMID: 8620612

5

Differential response to Na+ channel blockade, beta-adrenergic stimulation, and rapid pacing in a cellular model mimicking the SCN5A and HERG defects present in the long-QT syndrome.

Priori SG, Napolitano C, Cantù F, Brown AM, Schwartz PJ. Priori SG, et al. Among authors: schwartz pj. Circ Res. 1996 Jun;78(6):1009-15. doi: 10.1161/01.res.78.6.1009. Circ Res. 1996. PMID: 8635231

6

Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS.

Roden DM, Lazzara R, Rosen M, Schwartz PJ, Towbin J, Vincent GM. Roden DM, et al. Among authors: schwartz pj. Circulation. 1996 Oct 15;94(8):1996-2012. doi: 10.1161/01.cir.94.8.1996. Circulation. 1996. PMID: 8873679 Review.

7

New mutations in the KVLQT1 potassium channel that cause long-QT syndrome.

Li H, Chen Q, Moss AJ, Robinson J, Goytia V, Perry JC, Vincent GM, Priori SG, Lehmann MH, Denfield SW, Duff D, Kaine S, Shimizu W, Schwartz PJ, Wang Q, Towbin JA. Li H, et al. Among authors: schwartz pj. Circulation. 1998 Apr 7;97(13):1264-9. doi: 10.1161/01.cir.97.13.1264. Circulation. 1998. PMID: 9570196

8

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.

9

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.

Splawski I, Shen J, Timothy KW, Lehmann MH, Priori S, Robinson JL, Moss AJ, Schwartz PJ, Towbin JA, Vincent GM, Keating MT. Splawski I, et al. Among authors: schwartz pj. Circulation. 2000 Sep 5;102(10):1178-85. doi: 10.1161/01.cir.102.10.1178. Circulation. 2000. PMID: 10973849

10

A common polymorphism associated with antibiotic-induced cardiac arrhythmia.

Sesti F, Abbott GW, Wei J, Murray KT, Saksena S, Schwartz PJ, Priori SG, Roden DM, George AL Jr, Goldstein SA. Sesti F, et al. Among authors: schwartz pj. Proc Natl Acad Sci U S A. 2000 Sep 12;97(19):10613-8. doi: 10.1073/pnas.180223197. Proc Natl Acad Sci U S A. 2000. PMID: 10984545 Free PMC article.

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