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Last Updated: 10/31/2025

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Found 168 publications

Prognostic role of exercise intensity in familial Filamin C truncating variants.

Prognostic role of exercise intensity in familial Filamin C truncating variants.

Journal: Open heart
Published: June 26, 2025

KCNQ1 and GJA1 Variants Associated With Arrhythmogenic Right Ventricular Cardiomyopathy With a Lethal Outcome.

KCNQ1 and GJA1 Variants Associated With Arrhythmogenic Right Ventricular Cardiomyopathy With a Lethal Outcome.

Journal: JACC. Case reports
Published: June 19, 2025

Family Screening in Relatives at Risk for Plakophilin-2-Associated Arrhythmogenic Right Ventricular Cardiomyopathy.

Family Screening in Relatives at Risk for Plakophilin-2-Associated Arrhythmogenic Right Ventricular Cardiomyopathy.

Journal: Circulation
Published: June 17, 2025

Prolonged Extreme Asymptomatic Hypertroponinemia as a Milestone in Diagnosis of Familial Arrhythmogenic Right Ventricular Cardiomyopathy.

Prolonged Extreme Asymptomatic Hypertroponinemia as a Milestone in Diagnosis of Familial Arrhythmogenic Right Ventricular Cardiomyopathy.

Journal: Circulation. Heart failure
Published: May 30, 2025

A novel familial pathogenic desmoplakin (DSP) gene mutation (c.4751_4752del) presenting as "hot-phase" left-dominant arrhythmogenic cardiomyopathy.

A novel familial pathogenic desmoplakin (DSP) gene mutation (c.4751_4752del) presenting as "hot-phase" left-dominant arrhythmogenic cardiomyopathy.

Journal: Future cardiology
Published: May 05, 2025

Modified mRNA Treatment Restores Cardiac Function in Desmocollin-2-Deficient Mouse Models of Arrhythmogenic Right Ventricular Cardiomyopathy.

Modified mRNA Treatment Restores Cardiac Function in Desmocollin-2-Deficient Mouse Models of Arrhythmogenic Right Ventricular Cardiomyopathy.

Journal: Circulation
Published: April 11, 2025

Clinical Presentation and Long-Term Outcomes of Late-Onset Symptomatic ARVC.

Clinical Presentation and Long-Term Outcomes of Late-Onset Symptomatic ARVC.

Journal: JACC. Clinical electrophysiology
Published: March 01, 2025

Genetics in arrhythmogenic cardiomyopathies: where are we now and where are we heading to?

Genetics in arrhythmogenic cardiomyopathies: where are we now and where are we heading to?

Journal: European heart journal supplements : journal of the European Society of Cardiology
Published: February 21, 2025

Diagnostic and Prognostic Significance of miRNA-15a-5p, 16-5p, and 92a-3p in Arrhythmogenic Right Ventricular Cardiomyopathy.

Diagnostic and Prognostic Significance of miRNA-15a-5p, 16-5p, and 92a-3p in Arrhythmogenic Right Ventricular Cardiomyopathy.

Journal: Heart rhythm
Published: February 20, 2025

Diagnostic and prognostic significance of miRNA-15a-5p, 16-5p, and 92a-3p in arrhythmogenic right ventricular cardiomyopathy.

Diagnostic and prognostic significance of miRNA-15a-5p, 16-5p, and 92a-3p in arrhythmogenic right ventricular cardiomyopathy.

Journal: Heart rhythm
Published: February 20, 2025

The Future of Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-Cas9 Gene Therapy in Cardiomyopathies: A Review of Its Therapeutic Potential and Emerging Applications.

The Future of Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-Cas9 Gene Therapy in Cardiomyopathies: A Review of Its Therapeutic Potential and Emerging Applications.

Journal: Cureus
Published: February 19, 2025

China Multi-Center Cohort Study on Risk Evaluation of Arrhythmogenic Cardiomyopathy: The ChinaCORE ACM Registry.

China Multi-Center Cohort Study on Risk Evaluation of Arrhythmogenic Cardiomyopathy: The ChinaCORE ACM Registry.

Journal: JACC. Asia
Published: January 18, 2025
Showing 1-12 of 168

Last Updated: 10/31/2025