Elisa Mazzotti

Padova, 35121, Italy

Last Updated: 09/26/2026

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Found 12 publications

Circulating miR-185-5p as a Potential Biomarker for Arrhythmogenic Right Ventricular Cardiomyopathy.

Circulating miR-185-5p as a Potential Biomarker for Arrhythmogenic Right Ventricular Cardiomyopathy.

Journal: Cells
Published: August 17, 2021

Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy.

Whole-Exome Sequencing Identifies Pathogenic Variants in TJP1 Gene Associated With Arrhythmogenic Cardiomyopathy.

Journal: Circulation. Genomic and precision medicine
Published: October 26, 2018

A targeted next-generation gene panel reveals a novel heterozygous nonsense variant in the TP63 gene in patients with arrhythmogenic cardiomyopathy.

A targeted next-generation gene panel reveals a novel heterozygous nonsense variant in the TP63 gene in patients with arrhythmogenic cardiomyopathy.

Journal: Heart rhythm
Published: July 06, 2018

Co-inheritance of mutations associated with arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathy.

Co-inheritance of mutations associated with arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathy.

Journal: European journal of human genetics : EJHG
Published: February 20, 2017

Homozygous Desmocollin-2 Mutations and Arrhythmogenic Cardiomyopathy.

Homozygous Desmocollin-2 Mutations and Arrhythmogenic Cardiomyopathy.

Journal: The American journal of cardiology
Published: May 21, 2015

Phenotypic expression is a prerequisite for malignant arrhythmic events and sudden cardiac death in arrhythmogenic right ventricular cardiomyopathy.

Phenotypic expression is a prerequisite for malignant arrhythmic events and sudden cardiac death in arrhythmogenic right ventricular cardiomyopathy.

Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
Published: January 17, 2015

Compound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene-related arrhythmogenic right ventricular cardiomyopathy.

Compound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene-related arrhythmogenic right ventricular cardiomyopathy.

Journal: Circulation. Cardiovascular genetics
Published: September 28, 2013

Mutations in the area composita protein αT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy.

Mutations in the area composita protein αT-catenin are associated with arrhythmogenic right ventricular cardiomyopathy.

Journal: European heart journal
Published: November 09, 2012

Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy.

Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy.

Journal: European journal of human genetics : EJHG
Published: November 05, 2012

Noninvasive cardiac screening in young athletes with ventricular arrhythmias.

Noninvasive cardiac screening in young athletes with ventricular arrhythmias.

Journal: The American journal of cardiology
Published: September 26, 2012

Gender differences and role of pregnancy in the history of post-surgical women affected by tetralogy of Fallot.

Gender differences and role of pregnancy in the history of post-surgical women affected by tetralogy of Fallot.

Journal: PloS one
Published: May 30, 2012

Follow-up with exercise test of effort-induced ventricular arrhythmias linked to ryanodine receptor type 2 gene mutations.

Follow-up with exercise test of effort-induced ventricular arrhythmias linked to ryanodine receptor type 2 gene mutations.

Journal: The American journal of cardiology
Published: September 30, 2011
Showing 1-12 of 12

Last Updated: 09/26/2026