Prominent QTc prolongation in a patient with a rare variant in the cardiac ryanodine receptor gene

Clinical and Molecular Characterization of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

Silvia G. Priori, Carlo Napolitano, Mirella Memmi et al. · Circulation · 2002 · 1.2K citations

Medicine, Cardiology, Genetics +13

The RYR2-Encoded Ryanodine Receptor/Calcium Release Channel in Patients Diagnosed Previously With Either Catecholaminergic Polymorphic Ventricular Tachycardia or Genotype Negative, Exercise-Induced Long QT Syndrome

Argelia Medeiros‐Domingo, Zahurul A. Bhuiyan, David J. Tester et al. · Journal of the American College of Cardiology · 2009 · 337 citations · Full text

Medicine, Cardiology, Physiology +16

Spectrum and Frequency of Cardiac Channel Defects in Swimming-Triggered Arrhythmia Syndromes

Grace R. Choi, Laura J. Kopplin, David J. Tester et al. · Circulation · 2004 · 269 citations · Full text

Medicine, Cardiology, Genetics +16

HRS/EHRA/APHRS Expert Consensus Statement on the Diagnosis and Management of Patients with Inherited Primary Arrhythmia Syndromes

Silvia G. Priori, Arthur A.M. Wilde, Minoru Horie et al. · Journal of Arrhythmia · 2013 · 244 citations · Full text

Medicine, Cardiology, Genetics +17

Diagnostic value of epinephrine test for genotyping LQT1, LQT2, and LQT3 forms of congenital long QT syndrome

Wataru Shimizu, Takashi Noda, Hiroshi Takaki et al. · Heart Rhythm · 2004 · 184 citations

Life Sciences, Cardiology, Genetics +13