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Journal of Molecular and Cellular Cardiology|October 13, 2010
Calmodulin kinase II inhibition prevents arrhythmias in RyR2(R4496C+/-) mice with catecholaminergic polymorphic ventricular tachycardiaNian Liu, Yanfei Ruan, Marco Denegri, et al.
JAMA|January 18, 2006
Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practiceCarlo Napolitano, Silvia G Priori, Peter J Schwartz, et al.
Circulation Research|May 16, 2013
Abnormal propagation of calcium waves and ultrastructural remodeling in recessive catecholaminergic polymorphic ventricular tachycardiaNian Liu, Marco Denegri, Wen Dun, et al.
European Journal of Heart Failure|November 4, 2009
Implementation of device therapy (cardiac resynchronization therapy and implantable cardioverter defibrillator) for patients with heart failure in Europe: changes from 2004 to 2008Dirk J van Veldhuisen, Alexander H Maass, Silvia G Priori, et al.
Circulation|December 14, 2005
Cardiac histological substrate in patients with clinical phenotype of Brugada syndromeAndrea Frustaci, Silvia G Priori, Maurizio Pieroni, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|May 22, 2012
Late gadolinium enhancement by cardiovascular magnetic resonance is complementary to left ventricle ejection fraction in predicting prognosis of patients with stable coronary artery diseaseOronzo Catalano, Guido Moro, Mariarosa Perotti, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 5, 2004
A cardiac arrhythmia syndrome caused by loss of ankyrin-B functionPeter J Mohler, Igor Splawski, Carlo Napolitano, et al.
Studies in Health Technology and Informatics|September 1, 2016
Beyond Cohort Selection: An Analytics-Enabled i2b2Matteo Gabetta, Alberto Malovini, Mauro Bucalo, 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|September 10, 2021
Independent validation and clinical implications of the risk prediction model for long QT syndrome (1-2-3-LQTS-Risk)Andrea Mazzanti, Alessandro Trancuccio, Deni Kukavica, et al.
Human Mutation|April 4, 2003
A novel mutation L619F in the cardiac Na+ channel SCN5A associated with long-QT syndrome (LQT3): a role for the I-II linker in inactivation gatingXander H T Wehrens, Tom Rossenbacker, Roselie J Jongbloed, et al.
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