Advances in the diagnosis and treatment of catecholaminergic polymorphic ventricular tachycardia

scientific article published on January 2017

Advances in the diagnosis and treatment of catecholaminergic polymorphic ventricular tachycardia is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1017/S1047951116002237
P698PubMed publication ID28084961

P50authorShubhayan SanataniQ43748749
P2093author name stringThomas M Roston
Taylor C Cunningham
P2860cites workA cardiac arrhythmia syndrome caused by loss of ankyrin-B functionQ24295030
Mutations in calmodulin cause ventricular tachycardia and sudden cardiac deathQ24300356
Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in humanQ24307681
Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humansQ24608179
Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardiaQ28201561
A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from IsraelQ28204838
Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardiaQ28279395
Catecholaminergic polymorphic ventricular tachycardiaQ28287523
Inherited dysfunction of sarcoplasmic reticulum Ca2+ handling and arrhythmogenesisQ28308142
New exome data question the pathogenicity of genetic variants previously associated with catecholaminergic polymorphic ventricular tachycardiaQ30666264
Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal heartsQ33145152
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
A missense mutation in CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from IsraelQ33151465
Pathogenesis of unexplained drowning: new insights from a molecular autopsyQ33152673
Incidence and risk factors of arrhythmic events in catecholaminergic polymorphic ventricular tachycardiaQ33157356
Arrhythmia characterization and long-term outcomes in catecholaminergic polymorphic ventricular tachycardiaQ33159716
Therapeutic approach for patients with catecholaminergic polymorphic ventricular tachycardia: state of the art and future developmentsQ33160416
The role of stress test for predicting genetic mutations and future cardiac events in asymptomatic relatives of catecholaminergic polymorphic ventricular tachycardia probandsQ33161041
Familial evaluation in catecholaminergic polymorphic ventricular tachycardia: disease penetrance and expression in cardiac ryanodine receptor mutation-carrying relativesQ33161522
Effects of flecainide on exercise-induced ventricular arrhythmias and recurrences in genotype-negative patients with catecholaminergic polymorphic ventricular tachycardia.Q33162208
Outcomes of defibrillator therapy in catecholaminergic polymorphic ventricular tachycardia.Q33163389
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Catecholaminergic polymorphic ventricular tachycardia in children: analysis of therapeutic strategies and outcomes from an international multicenter registryQ33165339
Physical and Psychological Consequences of Left Cardiac Sympathetic Denervation in Long-QT Syndrome and Catecholaminergic Polymorphic Ventricular TachycardiaQ33166057
Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patientsQ33173888
The role of mutant protein level in autosomal recessive catecholamine dependent polymorphic ventricular tachycardia (CPVT2).Q33919062
Inhibition of cardiac Ca2+ release channels (RyR2) determines efficacy of class I antiarrhythmic drugs in catecholaminergic polymorphic ventricular tachycardia.Q34160930
Flecainide therapy reduces exercise-induced ventricular arrhythmias in patients with catecholaminergic polymorphic ventricular tachycardiaQ34629553
Arrhythmogenesis in a catecholaminergic polymorphic ventricular tachycardia mutation that depresses ryanodine receptor functionQ35279976
Thoracoscopic Left Cardiac Sympathetic Denervation for a Patient with Catecholaminergic Polymorphic Ventricular Tachycardia and Recurrent Implantable Cardioverter-Defibrillator Shocks.Q35720196
Implantable cardioverter-defibrillator harm in young patients with inherited arrhythmia syndromes: A systematic review and meta-analysis of inappropriate shocks and complicationsQ35781029
Psychological functioning and disease-related quality of life in pediatric patients with an implantable cardioverter defibrillatorQ35851697
A mechanism for sudden infant death syndrome (SIDS): stress-induced leak via ryanodine receptorsQ35904783
Loss of luminal Ca2+ activation in the cardiac ryanodine receptor is associated with ventricular fibrillation and sudden deathQ36156989
Assessing the knowledge of sudden unexpected death in the young among Canadian medical students and recent graduates: a cross-sectional studyQ36496344
In silico prediction of drug therapy in catecholaminergic polymorphic ventricular tachycardia.Q36667578
Molecular and electrophysiological bases of catecholaminergic polymorphic ventricular tachycardiaQ36853107
Catecholaminergic polymorphic ventricular tachycardia: A paradigm to understand mechanisms of arrhythmias associated to impaired Ca(2+) regulationQ37625277
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Efficacy of implantable cardioverter defibrillators in young patients with catecholaminergic polymorphic ventricular tachycardia: success depends on substrateQ38106029
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Early repolarization of surface ECG predicts fatal ventricular arrhythmias in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy and symptomatic ventricular arrhythmiasQ38987868
Ryanodine receptor mutations presenting as idiopathic ventricular fibrillation: a report on two novel familial compound mutations, c.6224T>C and c.13781A>G, with the clinical presentation of idiopathic ventricular fibrillationQ39172567
Implantable cardioverter-defibrillator explantation for overdiagnosed or overtreated congenital long QT syndromeQ40866214
Nadolol decreases the incidence and severity of ventricular arrhythmias during exercise stress testing compared with β1-selective β-blockers in patients with catecholaminergic polymorphic ventricular tachycardiaQ41268618
Single delivery of an adeno-associated viral construct to transfer the CASQ2 gene to knock-in mice affected by catecholaminergic polymorphic ventricular tachycardia is able to cure the disease from birth to advanced age.Q42215203
The human CASQ2 mutation K206N is associated with hyperglycosylation and altered cellular calcium handlingQ42469020
Genetic background of catecholaminergic polymorphic ventricular tachycardia in JapanQ44293793
Triadin overexpression stimulates excitation-contraction coupling and increases predisposition to cellular arrhythmia in cardiac myocytesQ44461573
Calcium channel antagonism reduces exercise-induced ventricular arrhythmias in catecholaminergic polymorphic ventricular tachycardia patients with RyR2 mutationsQ45273441
The direct actions of flecainide on the human cardiac ryanodine receptor: keeping open the debate on the mechanism of action of local anesthetics in CPVT.Q47723591
Gain-of-function mutation of the SCN5A gene causes exercise-induced polymorphic ventricular arrhythmiasQ48550349
Response to Letters Regarding Article, "Clinical Management of Catecholaminergic Polymorphic Ventricular Tachycardia: The Role of Left Cardiac Sympathetic Denervation".Q48747281
Flecainide monotherapy is an option for selected patients with catecholaminergic polymorphic ventricular tachycardia intolerant of β-blockadeQ59200864
Delay to diagnosis amongst patients with catecholaminergic polymorphic ventricular tachycardiaQ61632866
Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing catecholaminergic polymorphic ventricular tachycardiaQ62105551
Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardiaQ78390804
Molecular pathogenesis of catecholaminergic polymorphic ventricular tachycardia: sex matters!Q79833038
Prophylactic left thoracic sympathectomy to prevent electrical storms in CPVT patients needing ICD placementQ83816623
Importance of ventricular tachycardia storms not terminated by implantable cardioverter defibrillators shocks in patients with CASQ2 associated catecholaminergic polymorphic ventricular tachycardiaQ83821934
P433issueS1
P921main subjectcatecholaminergic polymorphic ventricular tachycardiaQ1649897
P304page(s)S49-S56
P577publication date2017-01-01
P1433published inCardiology in the YoungQ2041555
P1476titleAdvances in the diagnosis and treatment of catecholaminergic polymorphic ventricular tachycardia
P478volume27

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cites work (P2860)
Q64083681Catecholaminergic Polymorphic Ventricular Tachycardia: The Cardiac Arrest Where Epinephrine Is Contraindicated
Q57174642Novel approaches for the treatment of ventricular tachycardia

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