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Page 1
Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry.
Crotti L, Spazzolini C, Tester DJ, Ghidoni A, Baruteau AE, Beckmann BM, Behr ER, Bennett JS, Bezzina CR, Bhuiyan ZA, Celiker A, Cerrone M, Dagradi F, De Ferrari GM, Etheridge SP, Fatah M, Garcia-Pavia P, Al-Ghamdi S, Hamilton RM, Al-Hassnan ZN, Horie M, Jimenez-Jaimez J, Kanter RJ, Kaski JP, Kotta MC, Lahrouchi N, Makita N, Norrish G, Odland HH, Ohno S, Papagiannis J, Parati G, Sekarski N, Tveten K, Vatta M, Webster G, Wilde AAM, Wojciak J, George AL, Ackerman MJ, Schwartz PJ. Crotti L, et al. Among authors: al hassnan zn, george al, al ghamdi s. Eur Heart J. 2019 Sep 14;40(35):2964-2975. doi: 10.1093/eurheartj/ehz311. Eur Heart J. 2019. PMID: 31170290 Free PMC article.
Pharmacological targeting of long QT mutant sodium channels.
Wang DW, Yazawa K, Makita N, George AL Jr, Bennett PB. Wang DW, et al. Among authors: george al jr. J Clin Invest. 1997 Apr 1;99(7):1714-20. doi: 10.1172/JCI119335. J Clin Invest. 1997. PMID: 9120016 Free PMC article.
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: george al jr. 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.
Sudden cardiac death, genes, and arrhythmogenesis : consideration of new population and mechanistic approaches from a national heart, lung, and blood institute workshop, part I.
Spooner PM, Albert C, Benjamin EJ, Boineau R, Elston RC, George AL Jr, Jouven X, Kuller LH, MacCluer JW, Marbán E, Muller JE, Schwartz PJ, Siscovick DS, Tracy RP, Zareba W, Zipes DP. Spooner PM, et al. Among authors: george al jr. Circulation. 2001 May 15;103(19):2361-4. doi: 10.1161/01.cir.103.19.2361. Circulation. 2001. PMID: 11352884
Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype.
Zhang L, Benson DW, Tristani-Firouzi M, Ptacek LJ, Tawil R, Schwartz PJ, George AL, Horie M, Andelfinger G, Snow GL, Fu YH, Ackerman MJ, Vincent GM. Zhang L, et al. Among authors: george al. Circulation. 2005 May 31;111(21):2720-6. doi: 10.1161/CIRCULATIONAHA.104.472498. Epub 2005 May 23. Circulation. 2005. PMID: 15911703
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: george al jr. Circulation. 2005 Aug 30;112(9):1251-8. doi: 10.1161/CIRCULATIONAHA.105.549071. Epub 2005 Aug 22. Circulation. 2005. PMID: 16116052
450 results