Catecholaminergic polymorphic ventricular tachycardia, an update. (Q48161835)

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7 April 2020

title

Catecholaminergic polymorphic ventricular tachycardia, an update (English)

1 reference

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catecholaminergic polymorphic ventricular tachycardia

7 April 2020

main subject

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ventricular tachycardia

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1

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Marianne Penachini da Costa de Rezende Barbosa

7 April 2020

3

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7 April 2020

author name string

Raimundo Barbosa-Barros

2

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7 April 2020

Rodrigo Daminello-Raimundo

4

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7 April 2020

Augusto A de Lucca

5

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7 April 2020

Luiz C de Abreu

6

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7 April 2020

publication date

19 October 2017

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Annals of Noninvasive Electrocardiology

7 April 2020

published in

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volume

23

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issue

4

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page(s)

e12512

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The mechanism of flecainide action in CPVT does not involve a direct effect on RyR2.

7 April 2020

cites work

1 reference

Expanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic features

21 January 2018

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Exon 3 deletion of ryanodine receptor causes left ventricular noncompaction, worsening catecholaminergic polymorphic ventricular tachycardia, and sudden cardiac arrest.

21 January 2018

1 reference

Arrhythmogenic mechanisms in a mouse model of catecholaminergic polymorphic ventricular tachycardia

21 January 2018

1 reference

TECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT

21 January 2018

1 reference

A Missense Mutation in the CASQ2 Gene Is Associated with Autosomal-Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia

21 January 2018

1 reference

A type 2 ryanodine receptor variant associated with reduced Ca2 release and short-coupled torsades de pointes ventricular arrhythmia

21 January 2018

1 reference

The diagnostic utility of recovery phase QTc during treadmill exercise stress testing in the evaluation of long QT syndrome

21 January 2018

1 reference

Video-Assisted Thoracoscopic Left Cardiac Sympathetic Denervation in Patients with Hereditary Ventricular Arrhythmias.

21 January 2018

1 reference

Purkinje cells from RyR2 mutant mice are highly arrhythmogenic but responsive to targeted therapy

21 January 2018

1 reference

A Kir3.4 mutation causes Andersen-Tawil syndrome by an inhibitory effect on Kir2.1

21 January 2018

1 reference

Cell model of catecholaminergic polymorphic ventricular tachycardia reveals early and delayed afterdepolarizations

21 January 2018

1 reference

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

21 January 2018

1 reference

Molecular genetics of exercise-induced polymorphic ventricular tachycardia: identification of three novel cardiac ryanodine receptor mutations and two common calsequestrin 2 amino-acid polymorphisms

21 January 2018

1 reference

PKA phosphorylation dissociates FKBP12.6 from the calcium release channel (ryanodine receptor): defective regulation in failing hearts

21 January 2018

1 reference

Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death

21 January 2018

1 reference

Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compaction

21 January 2018

1 reference

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 fibrillation

21 January 2018

1 reference

Arrythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) and cathecholaminergic polymorphic ventricular tachycardia (CPVT): A phenotypic spectrum seen in same patient

21 January 2018

1 reference

Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients.

21 January 2018

1 reference

Inherited dysfunction of sarcoplasmic reticulum Ca2 handling and arrhythmogenesis

21 January 2018

1 reference

Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia.

21 January 2018

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Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes

21 January 2018

1 reference

Calcium channel blockers and beta-blockers versus beta-blockers alone for preventing exercise-induced arrhythmias in catecholaminergic polymorphic ventricular tachycardia

21 January 2018

1 reference

The clinical and genetic spectrum of catecholaminergic polymorphic ventricular tachycardia: findings from an international multicentre registry.

21 January 2018

1 reference

Cardiac sympathetic denervation to prevent life-threatening arrhythmias

21 January 2018

1 reference

Left cardiac sympathetic denervation in the management of high-risk patients affected by the long-QT syndrome

21 January 2018

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Catecholaminergic polymorphic ventricular tachycardia: electrocardiographic characteristics and optimal therapeutic strategies to prevent sudden death

21 January 2018

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Calcium channel antagonism reduces exercise-induced ventricular arrhythmias in catecholaminergic polymorphic ventricular tachycardia patients with RyR2 mutations

21 January 2018

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Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts

21 January 2018

1 reference

Targeted mutational analysis of the RyR2-encoded cardiac ryanodine receptor in sudden unexplained death: a molecular autopsy of 49 medical examiner/coroner's cases

21 January 2018

1 reference

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

21 January 2018

1 reference

Rapid adaptation of cardiac ryanodine receptors: modulation by Mg2 and phosphorylation

21 January 2018

1 reference

RyR2R420Q catecholaminergic polymorphic ventricular tachycardia mutation induces bradycardia by disturbing the coupled clock pacemaker mechanism

21 January 2018

1 reference

Effects of flecainide on exercise-induced ventricular arrhythmias and recurrences in genotype-negative patients with catecholaminergic polymorphic ventricular tachycardia.

21 January 2018

1 reference

Altered function and regulation of cardiac ryanodine receptors in cardiac disease

21 January 2018

1 reference

Channelopathies, genetic testing and risk stratification

21 January 2018

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Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype

21 January 2018

1 reference

Carvedilol and its new analogs suppress arrhythmogenic store overload-induced Ca2 release

21 January 2018

1 reference

Suppression-of-function mutations in the cardiac ryanodine receptor: Emerging evidence for a novel arrhythmia syndrome?

21 January 2018

1 reference

Interpreting Incidentally Identified Variants in Genes Associated With Catecholaminergic Polymorphic Ventricular Tachycardia in a Large Cohort of Clinical Whole-Exome Genetic Test Referrals

21 January 2018

1 reference

12 December 2020

Catecholaminergic polymorphic ventricular tachycardia in children: analysis of therapeutic strategies and outcomes from an international multicenter registry

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12 December 2020

Efficacy of Flecainide in the Treatment of Catecholaminergic Polymorphic Ventricular Tachycardia: A Randomized Clinical Trial

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12 December 2020

Genotypic heterogeneity and phenotypic mimicry among unrelated patients referred for catecholaminergic polymorphic ventricular tachycardia genetic testing

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12 December 2020

Distinct U wave changes in patients with catecholaminergic polymorphic ventricular tachycardia (CPVT)

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12 December 2020

Novel calmodulin mutations associated with congenital arrhythmia susceptibility

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12 December 2020

Familial evaluation in catecholaminergic polymorphic ventricular tachycardia: disease penetrance and expression in cardiac ryanodine receptor mutation-carrying relatives

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12 December 2020

Phenotype variability in patients carrying KCNJ2 mutations

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12 December 2020

Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia

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12 December 2020

Identifiers

DOI

10.1111/ANEC.12512

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29048771 AND SRC:MED&resulttype=core&format=json

7 April 2020

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29048771 AND SRC:MED&resulttype=core&format=json

7 April 2020

PubMed publication ID

29048771

1 reference