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

Current management of inherited arrhythmia syndromes associated with the cardiac ryanodine receptor.

Current opinion in cardiology - 1 Jul 2023

Przybylski Robert, Abrams Dominic J

Abstract excerpt

PURPOSE OF REVIEW: Gain-of-function variants in the gene encoding the cardiac ryanodine receptor ( RYR2 ) are associated with catecholaminergic polymorphic ventricular tachycardia (CPVT). The exercise stress test (EST) has long been fundamental in diagnosis and management, but recent work has further explored its role. A new entity termed calcium release deficiency syndrome (CRDS) has been associated with...

Read the complete abstract on PubMed

Topics

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

Share to Adrenergic beta-Antagonists
Share to Flecainide
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Ryanodine Receptor Calcium Release Channel

Share to Tachycardia, Ventricular

Source

Identifiers

PMID: 37016946
DOI: 10.1097/HCO.0000000000001051

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Current management of inherited arrhythmia syndromes associated with the cardiac ryanodine receptor.PMID 37016946Read ↗

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

Diverse Phenotypic Manifestations in a Family with a Novel RYR2 E4107A Variant.Semantic proximity Read ↗

Calcium Release Deficiency Syndrome: A New Inherited Arrhythmia Syndrome.Semantic proximity Read ↗

Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia.Semantic proximity Read ↗

Cardiac ryanodine receptor calcium release deficiency syndrome.Semantic proximity Read ↗

RYR2-ryanodinopathies: from calcium overload to calcium deficiency.Semantic proximity Read ↗

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

Genetics, manifestations, and management of catecholaminergic polymorphic ventricular tachycardia.Semantic proximity Read ↗

Clinical and Functional Characterization of Ryanodine Receptor 2 Variants Implicated in Calcium-Release Deficiency Syndrome.Semantic proximity Read ↗

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

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

Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing catecholaminergic polymorphic ventricular tachycardia.Semantic proximity Read ↗

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