Showing results (1-10 of 7) with videos related to
Sort By:
Pageof 1
The American Journal of Cardiology|April 13, 2011
Uncovering an intermediate phenotype associated with rs2200733 at 4q25 in lone atrial fibrillationAdele H Goodloe, Kathleen J Herron, Timothy M OlsonJournal of Cardiovascular Electrophysiology|February 13, 2008
X-linked nonsyndromic sinus node dysfunction and atrial fibrillation caused by emerin mutationMargaret L Karst, Kathleen J Herron, Timothy M OlsonJournal of Cardiovascular Electrophysiology|March 28, 2008
Lone atrial fibrillation: influence of familial disease on gender predilectionLin Y Chen, Kathleen J Herron, Bee C Tai, et al.Journal of the American College of Cardiology|August 29, 2009
Mutations in ribonucleic acid binding protein gene cause familial dilated cardiomyopathyKatharine M Brauch, Margaret L Karst, Kathleen J Herron, et al.Journal of the American College of Cardiology|June 25, 2003
Familial atrial fibrillation is a genetically heterogeneous disorderDawood Darbar, Kathleen J Herron, Jeffrey D Ballew, et al.JAMA|January 27, 2005
Sodium channel mutations and susceptibility to heart failure and atrial fibrillationTimothy M Olson, Virginia V Michels, Jeffrey D Ballew, et al.The New England Journal of Medicine|July 11, 2008
Atrial natriuretic peptide frameshift mutation in familial atrial fibrillationDenice M Hodgson-Zingman, Margaret L Karst, Leonid V Zingman, et al.Pageof 1