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Journal of Cardiovascular Electrophysiology|June 4, 2009
Mutations in conserved amino acids in the KCNQ1 channel and risk of cardiac events in type-1 long-QT syndromeChristian Jons, Arthur J Moss, Coeli M Lopes, et al.
Journal of the American College of Cardiology|February 25, 2003
Epinephrine unmasks latent mutation carriers with LQT1 form of congenital long-QT syndromeWataru Shimizu, Takashi Noda, Hiroshi Takaki, et al.
Human Molecular Genetics|December 10, 2008
Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformationsBhagyalaxmi Mohapatra, Brett Casey, Hua Li, et al.
Cardiovascular Toxicology|October 19, 2007
Myocardial Fas ligand expression increases susceptibility to AZT-induced cardiomyopathyEnkhsaikhan Purevjav, David P Nelson, Jacquelin J Varela, et al.
The Journal of Thoracic and Cardiovascular Surgery|February 27, 2007
Over two decades of pediatric heart transplantation: how has survival changed?David L S Morales, William J Dreyer, Susan W Denfield, et al.
Molecular Genetics and Metabolism|March 28, 2008
SCN5A variants in Japanese patients with left ventricular noncompaction and arrhythmiaLishen Shan, Naomasa Makita, Yanlin Xing, et al.
The New England Journal of Medicine|October 1, 1998
Influence of the genotype on the clinical course of the long-QT syndrome. International Long-QT Syndrome Registry Research GroupW Zareba, A J Moss, P J Schwartz, et al.
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