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Journal of Molecular and Cellular Cardiology|May 25, 2005
A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two familiesJeroen P P Smits, Tamara T Koopmann, Ronald Wilders, et al.
Circulation|February 2, 1999
Genetic and molecular basis of cardiac arrhythmias: impact on clinical management parts I and IIS G Priori, J Barhanin, R N Hauer, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 19, 2023
Strong enhancement of magnetic ordering temperature and structural/valence transitions in EuPd3S4 under high pressureShuyuan Huyan, Dominic H Ryan, Tyler J Slade, et al.
International Journal of Cardiology|December 8, 2023
Defibrillation threshold in elective subcutaneous implantable defibrillator generator replacements: Time to reduce the size of the pulse generator?W van der Stuijt, S Pepplinkhuizen, J A de Veld, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|August 29, 2022
Effectiveness and safety of mexiletine in patients at risk for (recurrent) ventricular arrhythmias: a systematic reviewMartijn H van der Ree, Laura van Dussen, Noa Rosenberg, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|March 17, 2010
How do hypertrophic cardiomyopathy mutations affect myocardial function in carriers with normal wall thickness? Assessment with cardiovascular magnetic resonanceTjeerd Germans, Iris K Rüssel, Marco J W Götte, et al.
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