Follow-up with exercise test of effort-induced ventricular arrhythmias linked to ryanodine receptor type 2 gene mutations

scientific article

Follow-up with exercise test of effort-induced ventricular arrhythmias linked to ryanodine receptor type 2 gene mutations is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1016/J.AMJCARD.2011.11.033
P932PMC publication ID3318118
P698PubMed publication ID22221940
P5875ResearchGate publication ID221726351

P50authorDomenico CorradoQ56529119
Gaetano ThieneQ29840356
Barbara BauceQ29840367
P2093author name stringAndrea Nava
Antonio Franco Folino
Cristina Basso
Luciano Daliento
Alessandra Rampazzo
Giorgia Beffagna
Elisa Carturan
Ilaria Rigato
Elisa Mazzotti
Alexandros Klavdios Steriotis
P2860cites workSudden cardiac death with normal heart: molecular autopsyQ33348909
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 wavesQ34145105
Flecainide therapy reduces exercise-induced ventricular arrhythmias in patients with catecholaminergic polymorphic ventricular tachycardiaQ34629553
Ventricular ectopy during treadmill exercise stress testing in the evaluation of long QT syndromeQ35762846
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 channelsQ37377209
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 screeningQ43182612
Denaturing HPLC-based approach for detecting RYR2 mutations involved in malignant arrhythmiasQ44886545
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 cardiomyopathyQ68030368
Ryanodine receptor dysfunction and triggered activity in the heartQ79451490
Mutant ryanodine receptors in catecholaminergic polymorphic ventricular tachycardia generate delayed afterdepolarizations due to increased propensity to Ca2+ wavesQ79906106
Ryanodine receptor (RyR2) mutations in sudden cardiac death: studies in extended pedigrees and phenotypic characterization in vitroQ84588014
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 humansQ24608179
Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardiaQ28142708
Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardiaQ28201561
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 tachycardiaQ28279395
Catecholaminergic polymorphic ventricular tachycardiaQ28287523
Arrhythmogenic mechanisms in a mouse model of catecholaminergic polymorphic ventricular tachycardiaQ28595062
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 casesQ33152066
Catecholaminergic polymorphic ventricular tachycardia from bedside to bench and beyondQ33156900
Incidence and risk factors of arrhythmic events in catecholaminergic polymorphic ventricular tachycardiaQ33157356
Arrhythmia characterization and long-term outcomes in catecholaminergic polymorphic ventricular tachycardiaQ33159716
P433issue7
P407language of work or nameEnglishQ1860
P921main subjectheart arrhythmiaQ189331
P304page(s)1015-1019
P577publication date2012-01-03
P1433published inAmerican Journal of CardiologyQ2208417
P1476titleFollow-up with exercise test of effort-induced ventricular arrhythmias linked to ryanodine receptor type 2 gene mutations
P478volume109

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cites work (P2860)
Q33161934A family with recurrent sudden death and no clinical clue.
Q38238961Sinus node dysfunction in catecholaminergic polymorphic ventricular tachycardia: risk factor and potential therapeutic target?

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