Browsing by Author "Sarquella Brugada, Geòrgia"
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The Role of clinical, genetic and segregation evaluation in sudden infant death

Post-mortem genetic analysis in juvenile cases of sudden cardiac death

Stop-Gain Mutations in PKP2 Are Associated with a Later Age of Onset of Arrhythmogenic Right Ventricular Cardiomyopathy

Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort

Genetics of channelopathies associated with sudden cardiac death

Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic Investigation

A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia

Cardiac Channelopathies and Sudden Death: Recent Clinical and Genetic Advances

Flecainide challenge in pediatric Brugada syndrome: adding further data to this diagnostic tool

DFP open access ​

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Molecular autopsy in sudden cardiac death

The utility of implantable loop recorder in the clinical management of pediatric patient with non-high-risk Brugada syndrome

DFP open access ​

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Characterization and Management of Arrhythmic Events in Young Patients With Brugada Syndrome

Personalized Interpretation and Clinical Translation of Genetic Variants Associated With Cardiomyopathies

Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare Variants

The presence of channelopathies in drowning and near-drowning-events in pediatric population

DFP open access ​

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Editorial: Paediatric arrhythmology: a challenge of the 21st century = Arritmología pediátrica, el reto del siglo XXI

Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes

Update on Genetic Basis of Brugada Syndrome: Monogenic, Polygenic or Oligogenic?

The role of remote rhythm monitoring during non-acute periods in patients with TANGO2-related metabolic encephalopathy and arrhythmias

DFP open access ​

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Unmasking paediatric tachycardias at home: applicability of the AliveCor outpatient ECG monitor for clinical management of neonates and infants with tachyarrhythmias

DFP open access ​

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Malignant Arrhythmogenic Role Associated with RBM20: A Comprehensive Interpretation Focused on a Personalized Approach

Pediatric Malignant Arrhythmias Caused by Rare Homozygous Genetic Variants in TRDN: A Comprehensive Interpretation

Rare Variants Associated with Arrhythmogenic Cardiomyopathy: Reclassification Five Years Later

Update on the Diagnostic Pitfalls of Autopsy and Post-Mortem Genetic Testing in Cardiomyopathies