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Journal of Structural Biology|September 2, 1998
Structural and functional responses of mammalian thick filaments to alterations in myosin regulatory light chainsR J Levine, Z Yang, N D Epstein, et al.Journal of Muscle Research and Cell Motility|March 3, 2001
R403Q and L908V mutant beta-cardiac myosin from patients with familial hypertrophic cardiomyopathy exhibit enhanced mechanical performance at the single molecule levelK A Palmiter, M J Tyska, J R Haeberle, et al.The American Journal of Cardiology|January 15, 1991
Sudden death during empiric amiodarone therapy in symptomatic hypertrophic cardiomyopathyL Fananapazir, M B Leon, R O Bonow, et al.Medical Physics|August 1, 1996
A Fourier based algorithm for tracking SPAMM tags in gated magnetic resonance cardiac imagesS Zhang, M A Douglas, L Yaroslavsky, et al.Journal of Molecular and Cellular Cardiology|September 1, 2000
Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathyT M Olson, T P Doan, N Y Kishimoto, et al.Pacing and Clinical Electrophysiology : PACE|March 1, 1985
Comparison of vitreous carbon and elgiloy transvenous ventricular pacing leadsA O Molajo, R J Bowes, L Fananapazir, et al.Circulation|June 1, 1988
Procainamide infusion test: inability to identify patients with Wolff-Parkinson-White syndrome who are potentially at risk of sudden deathL Fananapazir, D L Packer, L D German, et al.Circulation|May 1, 1991
Myocardial metabolic, hemodynamic, and electrocardiographic significance of reversible thallium-201 abnormalities in hypertrophic cardiomyopathyR O Cannon, V Dilsizian, P T O'Gara, et al.Circulation|February 1, 1992
Evidence of genetic heterogeneity in five kindreds with familial hypertrophic cardiomyopathyN D Epstein, L Fananapazir, H J Lin, et al.Circulation|November 1, 1989
Electrophysiologic abnormalities in patients with hypertrophic cardiomyopathy. A consecutive analysis in 155 patientsL Fananapazir, C M Tracy, M B Leon, et al.Pageof 8