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

The fifteen years of discoveries that shaped molecular electrophysiology: time for appraisal.

Circulation research - 20 Aug 2010

Priori Silvia G

Abstract excerpt

This article serves as an introductory overview to a thematic review series that will present the latest advancements in the field of inherited arrhythmias. This area of cardiac electrophysiology started approximately 15 years ago thanks to the contribution of Mark Keating and coworkers, who disc...

Read the complete abstract on PubMed

Topics

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

Share to Arrhythmias, Cardiac
Share to Electrophysiological Phenomena
Share to Genetic Testing

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Long QT Syndrome

Share to Mutation

Source

Identifiers

PMID: 20724724
DOI: 10.1161/CIRCRESAHA.110.226811

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20724724-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The fifteen years of discoveries that shaped molecular electrophysiology: time for appraisal.PMID 20724724Read ↗

Cardiac Channelopathies: Clinical Diagnosis and Promising Therapeutics.Semantic proximity Read ↗

Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel function.Semantic proximity Read ↗

Pathogenesis and Clinical Characteristics of Hereditary Arrhythmia Diseases.Semantic proximity Read ↗

Sudden cardiac death and inherited channelopathy: the basic electrophysiology of the myocyte and myocardium in ion channel disease.Semantic proximity Read ↗

Inherited ion channel diseases: a brief review.Semantic proximity Read ↗

Congenital long QT syndrome: a clinician's guide.Semantic proximity Read ↗

The long QT syndrome: ion channel diseases of the heart.Semantic proximity Read ↗

Molecular basis of arrhythmias.Semantic proximity Read ↗

Cardiac channelopathies: genetic and molecular mechanisms.Semantic proximity Read ↗

Electrical heart disease: Genetic and molecular basis of cardiac arrhythmias in normal structural hearts.Semantic proximity Read ↗

Potassium-channel mutations and cardiac arrhythmias--diagnosis and therapy.Semantic proximity Read ↗

Novel insights in the congenital long QT syndrome.Semantic proximity Read ↗

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