Francesca Brun

Trieste, Italy

Last Updated: 09/26/2026

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Found 29 publications

Genetic and Phenotypic Characterization of Nexilin (NEXN)-Related Cardiomyopathy: Results From a Multicentric Study.

Genetic and Phenotypic Characterization of Nexilin (NEXN)-Related Cardiomyopathy: Results From a Multicentric Study.

Journal: JACC. Heart failure

Published: November 20, 2024

Magnetic Resonance Imaging Characterization and Clinical Outcomes of Dilated and Arrhythmogenic Left Ventricular Cardiomyopathies.

Magnetic Resonance Imaging Characterization and Clinical Outcomes of Dilated and Arrhythmogenic Left Ventricular Cardiomyopathies.

Journal: Journal of the American College of Cardiology

Published: November 30, 2023

Impact of DCM-Causing Genetic Background on Long-Term Response to Cardiac Resynchronization Therapy.

Impact of DCM-Causing Genetic Background on Long-Term Response to Cardiac Resynchronization Therapy.

Journal: JACC. Clinical electrophysiology

Published: November 15, 2023

Prognostic Prediction of Genotype vs Phenotype in Genetic Cardiomyopathies.

Prognostic Prediction of Genotype vs Phenotype in Genetic Cardiomyopathies.

Journal: Journal of the American College of Cardiology

Published: June 21, 2022

Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants.

Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants.

Journal: Circulation

Published: September 30, 2021

Cardiac and Neuromuscular Features of Patients With LMNA-Related Cardiomyopathy.

Cardiac and Neuromuscular Features of Patients With LMNA-Related Cardiomyopathy.

Journal: Annals of internal medicine

Published: September 03, 2019

FLNC truncations cause arrhythmogenic right ventricular cardiomyopathy.

FLNC truncations cause arrhythmogenic right ventricular cardiomyopathy.

Journal: Journal of medical genetics

Published: July 04, 2019

Genetic Risk of Arrhythmic Phenotypes in Patients With Dilated Cardiomyopathy.

Genetic Risk of Arrhythmic Phenotypes in Patients With Dilated Cardiomyopathy.

Journal: Journal of the American College of Cardiology

Published: May 02, 2019

The S-wave angle identifies arrhythmogenic right ventricular cardiomyopathy in patients with electrocardiographically concealed disease phenotype.

The S-wave angle identifies arrhythmogenic right ventricular cardiomyopathy in patients with electrocardiographically concealed disease phenotype.

Journal: Journal of electrocardiology

Published: January 28, 2018

Filamin C Truncation Mutations Are Associated With Arrhythmogenic Dilated Cardiomyopathy and Changes in the Cell-Cell Adhesion Structures.

Filamin C Truncation Mutations Are Associated With Arrhythmogenic Dilated Cardiomyopathy and Changes in the Cell-Cell Adhesion Structures.

Journal: JACC. Clinical electrophysiology

Published: October 05, 2017

Right precordial-directed electrocardiographical markers identify arrhythmogenic right ventricular cardiomyopathy in the absence of conventional depolarization or repolarization abnormalities.

Right precordial-directed electrocardiographical markers identify arrhythmogenic right ventricular cardiomyopathy in the absence of conventional depolarization or repolarization abnormalities.

Journal: BMC cardiovascular disorders

Published: July 12, 2017

FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy.

FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy.

Journal: JACC. Basic to translational science

Published: December 23, 2016

Showing 1-12 of 29

Last Updated: 09/26/2026