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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. Among authors: schwartz pj. Circulation. 2007 Nov 20;116(21):2366-75. doi: 10.1161/CIRCULATIONAHA.107.726950. Epub 2007 Nov 5. Circulation. 2007. PMID: 17984373
Sudden death and the idiopathic long Q-T syndrome.
Moss AJ, Schwartz PJ. Moss AJ, et al. Among authors: schwartz pj. Am J Med. 1979 Jan;66(1):6-7. doi: 10.1016/0002-9343(79)90473-x. Am J Med. 1979. PMID: 420251 No abstract available.
The long QT syndrome. Prospective longitudinal study of 328 families.
Moss AJ, Schwartz PJ, Crampton RS, Tzivoni D, Locati EH, MacCluer J, Hall WJ, Weitkamp L, Vincent GM, Garson A Jr, et al. Moss AJ, et al. Among authors: schwartz pj. Circulation. 1991 Sep;84(3):1136-44. doi: 10.1161/01.cir.84.3.1136. Circulation. 1991. PMID: 1884444
641 results