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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 9, 2024. (Total: 231298Documents)
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Records 1 - 7 (of 7 Records)

Query Trace: Bundle-Branch Block and SCN5A[original query]
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
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
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
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
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
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
Susceptibility to Ventricular Arrhythmias Resulting from Mutations in FKBP1B, PXDNL, and SCN9A Evaluated in hiPSC Cardiomyocytes.
Stem cells international 2020 9 2020 8842398.
Barajas-Martinez Hector, Smith Maya, Hu Dan, Goodrow Robert J, Puleo Colleen, Hasdemir Can, Antzelevitch Charles, Pfeiffer Ryan, Treat Jacqueline A, Cordeiro Jonathan
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