Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mohammed Hajjiri"'
Autor:
Douglas Holmes, Larry A. Chinitz, Anthony Aizer, Neil E. Bernstein, Muhamed Saric, David S. Park, Mark Mascarenhas, Glenn Dym, Scott Bernstein, Steven J. Fowler, Mohammed Hajjiri, Ricardo Benenstein
Publikováno v:
Journal of Interventional Cardiac Electrophysiology. 40:147-151
Transesophageal echocardiography (TEE) is routinely used to assess for thrombus in the left atrium (LA) and left atrial appendage (LAA) in patients undergoing atrial fibrillation (AF) ablation. However, little is known about the outcome of AF ablatio
Autor:
Purva Agarwal, Tanya Ali, George O. Alonso, Ruben Alvero, Srivdya Anandan, Mel L. Anderson, Michelle Stozek Anvar, Kelly Bossenbrok, Maria A. Corigliano, George T. Danakas, Rami Eltibi, Mark J Fagan, Gil M. Farkash, Staci A. Fisher, Glenn G. Fort, Joseph Grillo, Mohammed Hajjiri, Sajeev Handa, Christine Hartley, Jennifer Jeremiah, Michael P. Johnson, Joseph Masci, Lonnie R. Mercier, Dennis Mickolich, James J. Ng, Gail M. O’Brien, Steven M. Opal, Pranav M. Patel, Eleni Patrozou, Peter Petropoulos, Arundathi G. Prasad, Deborah L. Shapiro, Jennifer Souther, Dominick Tammaro, Iris Tong, Tom Wachtel, Marie Elizabeth Wong
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7d34848b70bd05ca05cbf55b65f89203
https://doi.org/10.1016/b978-1-4377-0847-9.00003-9
https://doi.org/10.1016/b978-1-4377-0847-9.00003-9
Autor:
Naveed Rana, Malcolm Kirk, Gary F. Mitchell, Roland Macharzina, Mohammed Hajjiri, Athena Poppas, Katja E. Odening, Xuwen Peng, Michael Brunner, Eric Steinberg, Bum-Rak Choi, Rajesh Mathur, Gideon Koren, Tammy Donahay, Ohad Ziv, Eduardo J. Folco, Gongxin Liu, Manfred Zehender, Lorraine Schofield, Jason Centracchio, Xiao-Qin Ren, Ekatherini Pringa
Publikováno v:
The Journal of clinical investigation. 118(6)
Long QT syndrome (LQTS) is a heritable disease associated with ECG QT interval prolongation, ventricular tachycardia, and sudden cardiac death in young patients. Among genotyped individuals, mutations in genes encoding repolarizing K+ channels (LQT1: