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

Calmodulinopathy: A Novel, Life-Threatening Clinical Entity Affecting the Young

6 Dec 2018

Abstract excerpt

Sudden cardiac death (SCD) in the young may often be the first manifestation of a genetic arrythmogenic disease that had remained undiagnosed. Despite the significant discoveries of the genetic bases of inherited arrhythmia syndromes, there remains a measurable fraction of cases where in-depth clinical and genetic investigations fail to identify the underlying SCD etiology. A few years ago, 2 cases of infants...

Read the complete abstract on PubMed

Topics

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

Share to Cardiac electrophysiology and arrhythmias
Share to Cardiac pacing and defibrillation studies
Share to Cardiovascular Effects of Exercise

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 30574507
DOI: 10.3389/fcvm.2018.00175

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Calmodulinopathy: A Novel, Life-Threatening Clinical Entity Affecting the YoungPMID 30574507Read ↗

Calmodulin Mutations Associated with Heart Arrhythmia: A Status ReportSemantic proximity Read ↗

Role of Calmodulin in Cardiac Disease: Insights on Genotype and Phenotype.Semantic proximity Read ↗

Calmodulinopathy: Functional Effects of CALM Mutations and Their Relationship With Clinical PhenotypesSemantic proximity Read ↗

Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry.Semantic proximity Read ↗

Calmodulinopathy in Japanese Children - Their Cardiac Phenotypes Are Severe and Show Early Onset in Fetal Life and Infancy.Semantic proximity Read ↗

Calmodulin Mutations in Human Disease.Semantic proximity Read ↗

Novel calmodulin mutations associated with congenital arrhythmia susceptibility.Semantic proximity Read ↗

Calmodulin mutations associated with recurrent cardiac arrest in infants.Semantic proximity Read ↗

Genetic Mosaicism in CalmodulinopathySemantic proximity Read ↗

Novel calmodulin mutations associated with congenital long QT syndrome affect calcium current in human cardiomyocytes.Semantic proximity Read ↗

Spectrum and Prevalence of <i>CALM1</i> -, <i>CALM2</i> -, and <i>CALM3</i> -Encoded Calmodulin Variants in Long QT Syndrome and Functional Characterization of a Novel Long QT Syndrome–Associated Calmodulin Missense Variant, E141GSemantic proximity Read ↗

Calmodulin in a heartbeat.Semantic proximity Read ↗

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