Human Genome Epidemiology Literature Finder
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Query Trace: Bradycardia and KCNQ1[original query] |
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Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations. Journal of the American College of Cardiology 2004 Mar 43 (5): 826-30. Lupoglazoff JM, Denjoy I, Villain E, Fressart V, Simon F, Bozio A, Berthet M, Benammar N, Hainque B, Guicheney P |
Beta-blocker therapy failures in symptomatic probands with genotyped long-QT syndrome. Pediatric cardiology 0 25 (5): 459-65. Chatrath R, Bell C M, Ackerman M |
Torsades de pointes complicating atrioventricular block: evidence for a genetic predisposition. Heart rhythm : the official journal of the Heart Rhythm Society 2007 Feb 4 (2): 170-4. Chevalier Philippe, Bellocq Chloé, Millat Gilles, Piqueras Eric, Potet Franck, Schott Jean-Jacques, Baró Isabelle, Lemarec Hervé, Barhanin Jacques, Rousson Robert, Rodriguez-Lafrasse Clai |
Arrhythmia phenotype during fetal life suggests long-QT syndrome genotype: risk stratification of perinatal long-QT syndrome. Circulation. Arrhythmia and electrophysiology 2013 Aug . Cuneo BF, Etheridge SP, Horigome H, Sallee D, Moon-Grady A, Weng HY, Ackerman MJ, Benson DW |
The genetics underlying acquired long QT syndrome: impact for genetic screening. European heart journal 2015 Dec . Itoh Hideki, Crotti Lia, Aiba Takeshi, Spazzolini Carla, Denjoy Isabelle, Fressart Véronique, Hayashi Kenshi, Nakajima Tadashi, Ohno Seiko, Makiyama Takeru, Wu Jie, Hasegawa Kanae, Mastantuono Elisa, Dagradi Federica, Pedrazzini Matteo, Yamagishi Masakazu, Berthet Myriam, Murakami Yoshitaka, Shimizu Wataru, Guicheney Pascale, Schwartz Peter J, Horie Mino |
Autosomal recessive long QT syndrome, type 1 in eight families from Saudi Arabia. Molecular genetics & genomic medicine 2017 9 5 (5): 592-601. Bdier Amnah Y, Al-Ghamdi Saleh, Verma Prashant K, Dagriri Khalid, Alshehri Bandar, Jiman Omamah A, Ahmed Sherif E, Wilde Arthur A M, Bhuiyan Zahurul A, Al-Aama Jumana |
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