Back to search

Article

Epidemiology of Channelopathies in a Mediterranean Pediatric Population

2025-11-28

Abstract excerpt

<h4>Background: </h4> Channelopathies represent a heterogeneous group of rare inherited cardiac diseases associated with life-threatening arrhythmias. Our knowledge of their epidemiology in childhood is limited. The aim of this study is to evaluate the epidemiology of pediatric channelopathies on a Mediterranean island (Crete, Greece). <h4>Methods:</h4> Retrospective study of children &lt; 18 years followed in the...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
03847d7e-af16-543e-8198-aa43b5e044d7
DOI
10.20944/preprints202511.2256.v1
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Epidemiology of Channelopathies in a Mediterranean Pediatric PopulationDOI 10.20944/preprints202511.2256.v1
Cardiac channelopathies in pediatric patients - 7-years single center experience.Semantic proximity
Cardiac channelopathies in pediatrics: a genetic update.Semantic proximity
Clinical and Genetic Spectrums of Pediatric Cardiomyopathies: Experience from a Tertiary Pediatric Cardiology Centre in Hong KongSemantic proximity
Genetic Profile of Pediatric-Onset Cardiac ChannelopathiesSemantic proximity
Channelopathies in children and adults.Semantic proximity
Clinical and genetic profiles of chinese pediatric patients with catecholaminergic polymorphic ventricular tachycardia.Semantic proximity
SCN5A mutations in 442 neonates and children: genotype–phenotype correlation and identification of higher-risk subgroupsSemantic proximity
Clinical Spectrum of Arrhythmogenic Entities in Spanish Children Carrying Deleterious SCN5A Variants.Semantic proximity
Prognosis and clinical management of asymptomatic family members with RYR2-mediated catecholaminergic polymorphic ventricular tachycardia: a review.Semantic proximity
Diagnosis and management of patients with inherited arrhythmia syndromes in Europe: results of the European Heart Rhythm Association Survey.Semantic proximity
High Prevalence of Neurodevelopmental Disorders in Pediatric Long QT Syndrome: A Single Centre ExperienceSemantic proximity
Spectrum of genetic variants detected in children tested for long QT syndrome.Semantic proximity
Select a neighboring publication to make it the new centre.