Nuria Escute-Diez
Barcelona, CT, Spain
Last Updated: 09/26/2026
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Found 12 publications
Clinical Spectrum of Arrhythmogenic Entities in Spanish Children Carrying Deleterious SCN5A Variants.
Journal: International journal of molecular sciences
Published: December 23, 2025
Cardioneuroablation Restoring Atrioventricular Conduction in Brugada Syndrome: A Device-Free Approach.
Journal: JACC. Case reports
Published: November 17, 2025
Clinical usefulness of genetic diagnosis in early-onset cardiomyopathies.
Journal: Revista espanola de cardiologia (English ed.)
Published: August 25, 2025
Actionable Variants of Unknown Significance in Inherited Arrhythmogenic Syndromes: A Further Step Forward in Genetic Diagnosis.
Journal: Biomedicines
Published: October 15, 2024
Interpreting the actionable clinical role of rare variants associated with short QT syndrome.
Journal: Human genetics
Published: June 19, 2024
A narrative review of inherited arrhythmogenic syndromes in young population: role of genetic diagnosis in exercise recommendations.
Journal: BMJ open sport & exercise medicine
Published: June 11, 2024
Sex differences in long QT syndrome.
Journal: Frontiers in cardiovascular medicine
Published: February 11, 2023
Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohort.
Journal: International journal of legal medicine
Published: October 20, 2022
Structural Heart Alterations in Brugada Syndrome: Is it Really a Channelopathy? A Systematic Review.
Structural Heart Alterations in Brugada Syndrome: Is it Really a Channelopathy? A Systematic Review.
Journal: Journal of clinical medicine
Published: June 12, 2022
Brugada Syndrome in Women: What Do We Know After 30 Years?
Journal: Frontiers in cardiovascular medicine
Published: February 13, 2022
Showing 1-12 of 12
Last Updated: 09/26/2026