Martina Modena
Pisa, Italy
Last Updated: 09/26/2026
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Found 12 publications
A Novel Homozygous Mutation of the Desmoplakin Gene With Biventricular Arrhythmogenic Cardiomyopathy.
Journal: JACC. Case reports
Published: September 16, 2024
Whole-exome sequencing to identify causative variants in juvenile sudden cardiac death.
Journal: Human genomics
Published: June 04, 2024
Endocardial repolarization dispersion in BrS: A novel automatic algorithm for mapping activation recovery interval.
Journal: Journal of cardiovascular electrophysiology
Published: December 03, 2023
Effects of pirfenidone on scar size and ventricular remodeling after myocardial infarction: a preclinical study.
Journal: Journal of cardiovascular medicine (Hagerstown, Md.)
Published: November 09, 2023
Low HDL cholesterol and the eNOS Glu298Asp polymorphism are associated with inducible myocardial ischemia in patients with suspected stable coronary artery disease.
Journal: BMC cardiovascular disorders
Published: September 05, 2023
Understanding family history of heart disease: a (good) patient interview vs. genetics.
Journal: European journal of preventive cardiology
Published: May 13, 2023
Molecular Autopsy of Sudden Cardiac Death in the Genomics Era.
Journal: Diagnostics (Basel, Switzerland)
Published: May 20, 2021
Diffuse bone and soft tissue angiomatosis with GNAQ mutation.
Journal: Pathology international
Published: February 06, 2020
Unveiling a sudden unexplained death case by whole exome sequencing and bioinformatic analysis.
Journal: Molecular genetics & genomic medicine
Published: August 16, 2019
Cross-talk between pathogenic mechanisms in neurodegeneration: the role of oxidative stress in Amyotrophic Lateral Sclerosis.
Journal: Archives italiennes de biologie
Published: February 07, 2018
Showing 1-12 of 12
Last Updated: 09/26/2026