scholarly article | Q13442814 |
P50 | author | Domenico Corrado | Q56529119 |
Gaetano Thiene | Q29840356 | ||
Barbara Bauce | Q29840367 | ||
P2093 | author name string | Andrea Nava | |
Antonio Franco Folino | |||
Cristina Basso | |||
Luciano Daliento | |||
Alessandra Rampazzo | |||
Giorgia Beffagna | |||
Elisa Carturan | |||
Ilaria Rigato | |||
Elisa Mazzotti | |||
Alexandros Klavdios Steriotis | |||
P2860 | cites work | Sudden cardiac death with normal heart: molecular autopsy | Q33348909 |
In the RyR2(R4496C) mouse model of CPVT, β-adrenergic stimulation induces Ca waves by increasing SR Ca content and not by decreasing the threshold for Ca waves | Q34145105 | ||
Flecainide therapy reduces exercise-induced ventricular arrhythmias in patients with catecholaminergic polymorphic ventricular tachycardia | Q34629553 | ||
Ventricular ectopy during treadmill exercise stress testing in the evaluation of long QT syndrome | Q35762846 | ||
Ryanodine receptor-mediated arrhythmias and sudden cardiac death. | Q37248371 | ||
Regulation of basal and reserve cardiac pacemaker function by interactions of cAMP-mediated PKA-dependent Ca2+ cycling with surface membrane channels | Q37377209 | ||
Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients. | Q43073409 | ||
High prevalence of exercise-induced arrhythmias in catecholaminergic polymorphic ventricular tachycardia mutation-positive family members diagnosed by cascade genetic screening | Q43182612 | ||
Denaturing HPLC-based approach for detecting RYR2 mutations involved in malignant arrhythmias | Q44886545 | ||
Juvenile sudden death in a family with polymorphic ventricular arrhythmias caused by a novel RyR2 gene mutation: evidence of specific morphological substrates. | Q46638582 | ||
Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteria. | Q55638651 | ||
Juvenile sudden death and effort ventricular tachycardias in a family with right ventricular cardiomyopathy | Q68030368 | ||
Ryanodine receptor dysfunction and triggered activity in the heart | Q79451490 | ||
Mutant ryanodine receptors in catecholaminergic polymorphic ventricular tachycardia generate delayed afterdepolarizations due to increased propensity to Ca2+ waves | Q79906106 | ||
Ryanodine receptor (RyR2) mutations in sudden cardiac death: studies in extended pedigrees and phenotypic characterization in vitro | Q84588014 | ||
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) | Q24290749 | ||
Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans | Q24608179 | ||
Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia | Q28142708 | ||
Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia | Q28201561 | ||
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: a comprehensive open reading [...] | Q28265202 | ||
RyR2 mutations linked to ventricular tachycardia and sudden death reduce the threshold for store-overload-induced Ca2+ release (SOICR) | Q28278038 | ||
Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardia | Q28279395 | ||
Catecholaminergic polymorphic ventricular tachycardia | Q28287523 | ||
Arrhythmogenic mechanisms in a mouse model of catecholaminergic polymorphic ventricular tachycardia | Q28595062 | ||
Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia. | Q33147854 | ||
Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriers. | Q33147876 | ||
Targeted mutational analysis of the RyR2-encoded cardiac ryanodine receptor in sudden unexplained death: a molecular autopsy of 49 medical examiner/coroner's cases | Q33152066 | ||
Catecholaminergic polymorphic ventricular tachycardia from bedside to bench and beyond | Q33156900 | ||
Incidence and risk factors of arrhythmic events in catecholaminergic polymorphic ventricular tachycardia | Q33157356 | ||
Arrhythmia characterization and long-term outcomes in catecholaminergic polymorphic ventricular tachycardia | Q33159716 | ||
P433 | issue | 7 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | heart arrhythmia | Q189331 |
P304 | page(s) | 1015-1019 | |
P577 | publication date | 2012-01-03 | |
P1433 | published in | American Journal of Cardiology | Q2208417 |
P1476 | title | Follow-up with exercise test of effort-induced ventricular arrhythmias linked to ryanodine receptor type 2 gene mutations | |
P478 | volume | 109 |
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