HuGE Literature Finder
Records 1-6
|
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 |
|
H558R polymorphism in SCN5A is associated with Keshan disease and QRS prolongation in Keshan disease patients.
Genetics and molecular research : GMR 2014 13 (3): 6569-76. Jiang S, Li F L, Dong Q, Liu H W, Fang C F, Shu C, Cheng H, Cui J, Ma H X, Chen D Q, Li |
|
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 |
|
Parental electrocardiographic screening identifies a high degree of inheritance for congenital and childhood nonimmune isolated atrioventricular block.
Circulation 2012 Sep 126 (12): 1469-77. Baruteau Alban-Elouen, Behaghel Albin, Fouchard Swanny, Mabo Philippe, Schott Jean-Jacques, Dina Christian, Chatel Stéphanie, Villain Elisabeth, Thambo Jean-Benoit, Marçon François, Gournay Véronique, Rouault Francis, Chantepie Alain, Guillaumont Sophie, Godart François, Martins Raphaël P, Delasalle Béatrice, Bonnet Caroline, Fraisse Alain, Schleich Jean-Marc, Lusson Jean-René, Dulac Yves, Daubert Jean-Claude, Le Marec Hervé, Probst Vince |
|
Differential effects of cardiac sodium channel mutations on initiation of ventricular arrhythmias in patients with Brugada syndrome.
Heart rhythm : the official journal of the Heart Rhythm Society 2009 Apr 6 (4): 4. Morita H, Nagase S, Miura D, Miura A, Hiramatsu S, Tada T, Murakami M, Nishii N, Nakamura K, Morita ST, Oka T, Kusano KF, Ohe T |
|
Sodium channel gene (SCN5A) mutations in 44 index patients with Brugada syndrome: different incidences in familial and sporadic disease.
Human mutation 2003 Jun 21 (6): 651-2. Schulze-Bahr Eric, Eckardt Lars, Breithardt Günter, Seidl Karlheinz, Wichter Thomas, Wolpert Christian, Borggrefe Martin, Haverkamp Wilhe |
- Page last reviewed:Oct 1, 2020
- Page last updated:Oct 14, 2020
- Content source: