Publications by authors named "Victoria Fiol"

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Sex differences in long QT syndrome.
Nuria Díez-Escuté, Elena Arbelo, Estefanía Martínez-Barrios, Patricia Cerralbo, Sergi Cesar, Victoria Fiol

Front Cardiovasc Med· April 2023

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Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohort.
Estefanía Martinez-Barrios, Georgia Sarquella-Brugada, Alexandra Perez-Serra, Anna Fernandez-Falgueras, Sergi Cesar, Victoria Fiol

Int J Legal Med· March 2023

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-related muscular dystrophy: Identification of variants in alternative genes and personalized clinical translation.
Sergi Cesar, Monica Coll, Victoria Fiol, Anna Fernandez-Falgueras, Jose Cruzalegui

Front Genet· March 2023

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Clinical impact of rare variants associated with inherited channelopathies: a 5-year update.
Georgia Sarquella-Brugada, Anna Fernandez-Falgueras, Sergi Cesar, Elena Arbelo, Mónica Coll, Victoria Fiol

Hum Genet· October 2022

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Structural Heart Alterations in Brugada Syndrome: Is it Really a Channelopathy? A Systematic Review.
Antonio Oliva, Simone Grassi, Vilma Pinchi, Francesca Cazzato, Mónica Coll, Victoria Fiol

J Clin Med· July 2022

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Pediatric Left Posteroseptal Accessory Pathway Ablation from Giant Coronary Sinus with Persistent Left Superior Cava.
José Cruzalegui, Sergi Cesar, Oscar Campuzano, Victoria Fiol, Josep Brugada

J Cardiovasc Dev Dis· April 2022

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Brugada Syndrome in Women: What Do We Know After 30 Years?
Estefanía Martínez-Barrios, Elena Arbelo, Sergi Cesar, José Cruzalegui, Victoria Fiol

Front Cardiovasc Med· April 2022

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Discerning the Ambiguous Role of Missense Variants in Inherited Arrhythmogenic Syndromes.
Estefanía Martínez-Barrios, Georgia Sarquella-Brugada, Alexandra Pérez-Serra, Anna Fernández-Falgueras, Sergi Cesar, Victoria Fiol

J Pers Med· February 2022

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Clinical Genetics of Inherited Arrhythmogenic Disease in the Pediatric Population.
Estefanía Martínez-Barrios, Sergi Cesar, José Cruzalegui, Clara Hernandez, Elena Arbelo, Victoria Fiol

Biomedicines· January 2022

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Early Identification of Prolonged QT Interval for Prevention of Sudden Infant Death.
Georgia Sarquella-Brugada, Oscar García-Algar, María Dolores Zambrano, Anna Fernández-Falgueres, Sebastian Sailer, Victoria Fiol

Front Pediatr· July 2021

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Rare Variants Associated with Arrhythmogenic Cardiomyopathy: Reclassification Five Years Later.
Marta Vallverdú-Prats, Mireia Alcalde, Georgia Sarquella-Brugada, Sergi Cesar, Elena Arbelo, Victoria Fiol

J Pers Med· February 2021

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Pediatric Malignant Arrhythmias Caused by Rare Homozygous Genetic Variants in : A Comprehensive Interpretation.
Georgia Sarquella-Brugada, Anna Fernandez-Falgueras, Sergi Cesar, Elena Arbelo, Paloma Jordà, Victoria Fiol

Front Pediatr· February 2021

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Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?
Jesus Mates, Irene Mademont-Soler, Anna Fernandez-Falgueras, Georgia Sarquella-Brugada, Sergi Cesar, Victoria Fiol

Forensic Sci Int Genet· July 2020

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Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare Variants.
Oscar Campuzano, Anna Fernandez-Falgueras, Ximena Lemus, Georgia Sarquella-Brugada, Sergi Cesar, Victoria Fiol

J Clin Med· July 2019

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Genetic interpretation and clinical translation of minor genes related to Brugada syndrome.
Oscar Campuzano, Georgia Sarquella-Brugada, Anna Fernandez-Falgueras, Sergi Cesar, Monica Coll, Victoria Fiol

Hum Mutat· June 2019

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Personalized Interpretation and Clinical Translation of Genetic Variants Associated With Cardiomyopathies.
Oscar Campuzano, Anna Fernandez-Falgueras, Georgia Sarquella-Brugada, Sergi Cesar, Elena Arbelo, Victoria Fiol

Front Genet· May 2019

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Electrocardiographic Assessment and Genetic Analysis in Neonates: a Current Topic of Discussion.
Georgia Sarquella-Brugada, Sergi Cesar, Maria Dolores Zambrano, Anna Fernandez-Falgueras, Victoria Fiol

Curr Cardiol Rev· January 2019

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