Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Flecainide in patient with aggressive catecholaminergic polymorphic ventricular tachycardia due to novel RYR2 mutation.

Minerva cardioangiologica - 1 Aug 2014

Wangüemert-Pérez F, Ruiz-Hernández P M, Campuzano O, Caballero-Dorta E, Bosch C, Brugada J, Brugada R

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Anti-Arrhythmia Agents
Share to Electrocardiography
Share to Flecainide
Share to RYR2 gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Polymorphic Catecholaminergic Ventricular Tachycardia

Share to Ryanodine Receptor Calcium Release Channel

Share to Tachycardia, Ventricular

Source

Identifiers

PMID: 25012103

Genes

RYR2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Flecainide in patient with aggressive catecholaminergic polymorphic ventricular tachycardia due to novel RYR2 mutation.PMID 25012103Read ↗

Catecholaminergic polymorphic ventricular tachycardia: a model for genotype-specific therapy.Semantic proximity Read ↗

Catecholaminergic Polymorphic Ventricular Tachycardia: A Review of Therapeutic Strategies.Semantic proximity Read ↗

Flecainide Reduces Ventricular Arrhythmias in Patients With Genotype RyR2-positive Catecholaminergic Polymorphic Ventricular Tachycardia.Semantic proximity Read ↗

Flecainide for recurrent malignant ventricular arrhythmias in two siblings with Andersen-Tawil syndrome.Semantic proximity Read ↗

Cardiac ryanodine receptor gene (hRyR2) mutation underlying catecholaminergic polymorphic ventricular tachycardia in a Chinese adolescent presenting with sudden cardiac arrest and cardiac syncope.Semantic proximity Read ↗

Catecholaminergic Polymorphic Ventricular Tachycardia.Semantic proximity Read ↗

Advances in the diagnosis and treatment of catecholaminergic polymorphic ventricular tachycardia.Semantic proximity Read ↗

50 Years of Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) - Time to Explore the Dark Side of the Moon.Semantic proximity Read ↗

Guidelines for the diagnosis and management of Catecholaminergic Polymorphic Ventricular Tachycardia.Semantic proximity Read ↗

[Recurrent syncope related to catecholaminergic polymorphic ventricular tachycardia due to de novo RyR2-R2401H mutation].Semantic proximity Read ↗

Insights on the mechanism of flecainide in catecholaminergic polymorphic ventricular tachycardia.Semantic proximity Read ↗

A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.