HuGE Literature Finder
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Records 1-22
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Correlations of SCN5A gene polymorphisms with onset of atrial fibrillation.
European review for medical and pharmacological sciences 2019 Aug 23 (16): 7089-7097. Wang X-J, Ding P, Wang F-Z, Liu |
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Surveillance after cardiac arrest in patients with Brugada syndrome without an implantable defibrillator: An alarm effect of the previous syncope.
International journal of cardiology 2016 May 218 69-74. Calvo David, Flórez Juan Pablo, Valverde Irene, Rubín José, Pérez Diego, Vasserot Mar Gonzalez, Rodríguez-Reguero Julián, Avanzas Pablo, de la Hera Jesús María, Gómez Juan, Coto Eliecer, Martínez-Camblor Pablo, Morís Cés |
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The Influence of Pregnancy in Patients with Congenital Long QT Syndrome.
Cardiology in review 2016 Mar . Garg Lohit, Garg Jalaj, Krishnamoorthy Parasuram, Ahnert Amy, Shah Neeraj, Dusaj Raman S, Bozorgnia Bab |
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Novel SCN10A variants associated with Brugada syndrome.
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2015 Apr . Fukuyama Megumi, Ohno Seiko, Makiyama Takeru, Horie Mino |
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Mutation Analysis of KCNQ1, KCNH2 and SCN5A Genes in Taiwanese Long QT Syndrome Patients.
International heart journal 2015 56 (4): 450-3. Chang Ya-Sian, Yang Yi-Wen, Lin Yen-Nien, Lin Kuo-Hung, Chang Kuan-Cheng, Chang Jan-Gow |
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Prevalence and prognostic role of various conduction disturbances in patients with the Brugada syndrome.
The American journal of cardiology 2013 Nov 112 (9): 1384-9. Maury Philippe, Rollin Anne, Sacher Frédéric, Gourraud Jean-Baptiste, Raczka Franck, Pasquié Jean-Luc, Duparc Alexandre, Mondoly Pierre, Cardin Christelle, Delay Marc, Derval Nicolas, Chatel Stéphanie, Bongard Vanina, Sadron Marie, Denis Arnaud, Davy Jean-Marc, Hocini Mélèze, Jaïs Pierre, Jesel Laurence, Haïssaguerre Michel, Probst Vince |
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Results of genetic testing in 855 consecutive unrelated patients referred for long QT syndrome in a clinical laboratory.
Genetic testing and molecular biomarkers 2013 Jul 17 (7): 553-61. Lieve Krystien V, Williams Leah, Daly Amy, Richard Gabriele, Bale Sherri, Macaya Daniela, Chung Wendy |
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A study of the SCN5A gene in a cohort of 76 patients with Brugada syndrome.
Clinical genetics 2013 Jun 83 (6): 530-8. García-Molina E, Lacunza J, Ruiz-Espejo F, Sabater M, García-Alberola A, Gimeno J R, Cañizares F, García A, Martínez P, Valdés M, Tovar |
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L-type calcium channel mutations in Japanese patients with inherited arrhythmias.
Circulation journal : official journal of the Japanese Circulation Society 2013 77 (7): 1799-806. Fukuyama Megumi, Ohno Seiko, Wang Qi, Kimura Hiromi, Makiyama Takeru, Itoh Hideki, Ito Makoto, Horie Mino |
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Novel SCN3B Mutation Associated With Brugada Syndrome Affects Intracellular Trafficking and Function of Nav1.5.
Circulation journal : official journal of the Japanese Circulation Society 2012 Dec . Ishikawa T, Takahashi N, Ohno S, Sakurada H, Nakamura K, On YK, Park JE, Makiyama T, Horie M, Arimura T, Makita N, Kimura A |
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Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing.
BMC cardiovascular disorders 2012 12 (1): 95. Stattin Eva-Lena, Boström Ida Maria, Winbo Annika, Cederquist Kristina, Jonasson Jenni, Jonsson Björn-Anders, Diamant Ulla-Britt, Jensen Steen M, Rydberg Annika, Norberg An |
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Prevalence and spectrum of large deletions or duplications in the major long QT syndrome-susceptibility genes and implications for long QT syndrome genetic testing.
The American journal of cardiology 2010 Oct 106 (8): 1124-8. Tester David J, Benton Amber J, Train Laura, Deal Barbara, Baudhuin Linnea M, Ackerman Michael |
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Torsades de pointes during complete atrioventricular block: Genetic factors and electrocardiogram correlates.
The Canadian journal of cardiology 2010 Apr 26 (4): 208-12. Subbiah Rajesh N, Gollob Michael H, Gula Lorne J, Davies Robert W, Leong-Sit Peter, Skanes Allan C, Yee Raymond, Klein George J, Krahn Andrew |
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Mutation analysis of KCNQ1, KCNH2, SCN5A, KCNE1 and KCNE2 genes in Chinese patients with long QT syndrome.
Frontiers of medicine in China 2007 Jul 1 (3): 312-5. Du Rong, Tian Li, Yuan Guohui, Li Jin, Ren Faxin, Gui Le, Li Wei, Zhang Shouyan, Kang Cailian, Yang Jung |
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Allelic variants of SCN5A and risk of sudden cardiac arrest in patients with coronary artery disease.
Heart rhythm : the official journal of the Heart Rhythm Society 2006 Jun 3 (6): 697-700. Stecker Eric C, Sono Megan, Wallace Erin, Gunson Karen, Jui Jonathan, Chugh Sumeet |
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The long QT syndrome family of cardiac ion channelopathies: a HuGE review.
Genetics in medicine : official journal of the American College of Medical Genetics 2006 Mar 8 (3): 143-55. Modell Stephen M, Lehmann Michael |
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Double SCN5A mutation underlying asymptomatic Brugada syndrome.
Heart rhythm : the official journal of the Heart Rhythm Society 2005 Mar 2 (3): 285-92. Yokoi Hisataka, Makita Naomasa, Sasaki Koji, Takagi Yasuhiro, Okumura Yasuo, Nishino Tetsuo, Makiyama Takeru, Kitabatake Akira, Horie Minoru, Watanabe Ichiro, Tsutsui Hiroyu |
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Identification of a common genetic substrate underlying postpartum cardiac events in congenital long QT syndrome.
Heart rhythm : the official journal of the Heart Rhythm Society 2004 May 1 (1): 60-4. Khositseth Anant, Tester David J, Will Melissa L, Bell Carla M, Ackerman Michael |
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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 |
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Modulating effects of age and gender on the clinical course of long QT syndrome by genotype.
Journal of the American College of Cardiology 2003 Jul 42 (1): 103-9. Zareba Wojciech, Moss Arthur J, Locati Emanuela H, Lehmann Michael H, Peterson Derick R, Hall W Jackson, Schwartz Peter J, Vincent G Michael, Priori Silvia G, Benhorin Jesaia, Towbin Jeffrey A, Robinson Jennifer L, Andrews Mark L, Napolitano Carlo, Timothy Katherine, Zhang Li, Medina Aharon, |
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Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.
Circulation 2001 Jan 103 (1): 89-95. Schwartz P J, Priori S G, Spazzolini C, Moss A J, Vincent G M, Napolitano C, Denjoy I, Guicheney P, Breithardt G, Keating M T, Towbin J A, Beggs A H, Brink P, Wilde A A, Toivonen L, Zareba W, Robinson J L, Timothy K W, Corfield V, Wattanasirichaigoon D, Corbett C, Haverkamp W, Schulze-Bahr E, Lehmann M H, Schwartz K, Coumel P, Bloise |
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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 |
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- Page last updated:Oct 10, 2019
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