HuGE Literature Finder
Records 1-5
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An investigation of the association of the H558R polymorphism of the SCN5A gene with idiopathic cardiac conduction disorders.
Genetic testing and molecular biomarkers 2015 Jun 19 (6): 288-94. Nikulina Svetlana Y, Chernova Anna A, Shulman Vladimir A, Maksimov Vladimir N, Gavrilyuk Oksana A, Tretyakova Svetlana S, Marilovceva Olga |
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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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Arrhythmia Phenotype during Fetal Life Suggests LQTS 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 |
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A1180V of cardiac sodium channel gene (SCN5A): is it a risk factor for dilated cardiomyopathy or just a common variant in Han Chinese?
Disease markers 2013 35 (5): 531-5. Shen Cheng, Xu Lei, Yang Zhiyin, Zou Yunzeng, Hu Kai, Fan Zheng, Ge Junbo, Sun Aij |
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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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- Page last updated:Oct 23, 2020
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