Catecholamineinduced severe ventricular arrhythmias with Adams-Stokes syndrome in children: report of four cases, Br Heart J, vol.40, pp.28-37, 1978. ,
Catecholaminergic Polymorphic Ventricular Tachycardia in Children : A 7-Year Follow-up of 21 Patients, Circulation, vol.91, issue.5, pp.1512-1519, 1995. ,
DOI : 10.1161/01.CIR.91.5.1512
Mutations of the Cardiac Ryanodine Receptor (RyR2) Gene in Familial Polymorphic Ventricular Tachycardia, Circulation, vol.103, issue.4, pp.485-490, 2001. ,
DOI : 10.1161/01.CIR.103.4.485
Mutations in the Cardiac Ryanodine Receptor Gene (hRyR2) Underlie Catecholaminergic Polymorphic Ventricular Tachycardia, Circulation, vol.103, issue.2, pp.196-200, 2001. ,
DOI : 10.1161/01.CIR.103.2.196
A Missense Mutation in a Highly Conserved Region of CASQ2 Is Associated with Autosomal Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia in Bedouin Families from Israel, The American Journal of Human Genetics, vol.69, issue.6, pp.1378-1384, 2001. ,
DOI : 10.1086/324565
Absence of Calsequestrin 2 Causes Severe Forms of Catecholaminergic Polymorphic Ventricular Tachycardia, Circulation Research, vol.91, issue.8, pp.21-26, 2002. ,
DOI : 10.1161/01.RES.0000038886.18992.6B
Spectrum and Frequency of Cardiac Channel Defects in Swimming-Triggered Arrhythmia Syndromes, Circulation, vol.110, issue.15, pp.2119-2124, 2004. ,
DOI : 10.1161/01.CIR.0000144471.98080.CA
Spectrum and prevalence of cardiac ryanodine receptor (RyR2) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testing, Heart Rhythm, vol.2, issue.10, pp.1099-1105, 2005. ,
DOI : 10.1016/j.hrthm.2005.07.012
Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death, Journal of the American College of Cardiology, vol.40, issue.2, pp.341-349, 2002. ,
DOI : 10.1016/S0735-1097(02)01946-0
Autosomal Recessive Catecholamine- or Exercise-Induced Polymorphic Ventricular Tachycardia : Clinical Features and Assignment of the Disease Gene to Chromosome 1p13-21, Circulation, vol.103, issue.23, pp.2822-2827, 2001. ,
DOI : 10.1161/01.CIR.103.23.2822
Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients, Journal of Medical Genetics, vol.42, issue.11, pp.863-870, 2005. ,
DOI : 10.1136/jmg.2004.028993
Clinical and Molecular Characterization of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia, Circulation, vol.106, issue.1, pp.69-74, 2002. ,
DOI : 10.1161/01.CIR.0000020013.73106.D8
Catecholaminergic polymorphic ventricular tachycardia: electrocardiographic characteristics and optimal therapeutic strategies to prevent sudden death, Heart, vol.89, issue.1, pp.66-70, 2003. ,
DOI : 10.1136/heart.89.1.66
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1767500
Arrhythmic disorder mapped to chromosome 1q42???q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts, Journal of the American College of Cardiology, vol.34, issue.7, pp.2035-2042, 1999. ,
DOI : 10.1016/S0735-1097(99)00461-1
Recommendations for Physical Activity and Recreational Sports Participation for Young Patients With Genetic Cardiovascular Diseases, Circulation, vol.109, issue.22, pp.2807-2816, 2004. ,
DOI : 10.1161/01.CIR.0000128363.85581.E1
Nonparametric Estimation from Incomplete Observations, Journal of the American Statistical Association, vol.37, issue.282, pp.457-481, 1958. ,
DOI : 10.1214/aoms/1177731566
Regression models and lifetables, J R Stat Soc (B), vol.34, pp.187-220, 1972. ,
Calcium channel blockers and beta-blockers versus beta-blockers alone for preventing exercise-induced arrhythmias in catecholaminergic polymorphic ventricular tachycardia, Heart Rhythm, vol.4, issue.9, pp.1149-1154, 2007. ,
DOI : 10.1016/j.hrthm.2007.05.017
Calcium Channel Antagonism Reduces Exercise-Induced Ventricular Arrhythmias in Catecholaminergic Polymorphic Ventricular Tachycardia Patients with RyR2 Mutations, Journal of Cardiovascular Electrophysiology, vol.193, issue.2, pp.162-166, 2005. ,
DOI : 10.1016/S0002-9149(96)00011-2