Arrhythmogenic Right Ventricular Cardiomyopathy Latest Advances

Find the Latest Research About Arrhythmogenic Right Ventricular Cardiomyopathy

Last Updated: 04/28/2026

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Found 170 publications

Newfoundland Mutation TMEM43-p.S358L Causes Impaired Cardiac Energy Metabolism and Mitochondrial Function Through Altered Protein Interaction.

Newfoundland Mutation TMEM43-p.S358L Causes Impaired Cardiac Energy Metabolism and Mitochondrial Function Through Altered Protein Interaction.

Journal: Circulation. Genomic and precision medicine
Published: April 01, 2026

Imaging Naxos Disease and Related Cardiocutaneous Syndromes: The NAXCARE Multimodality Approach.

Imaging Naxos Disease and Related Cardiocutaneous Syndromes: The NAXCARE Multimodality Approach.

Journal: Hellenic journal of cardiology : HJC = Hellenike kardiologike epitheorese
Published: February 04, 2026

Pediatric Stroke Associated With a Rare Pathogenic PKP2 Variant: A Diagnostic Challenge.

Pediatric Stroke Associated With a Rare Pathogenic PKP2 Variant: A Diagnostic Challenge.

Journal: Cureus
Published: January 29, 2026

Case Report: Contrasting phenotypes of arrhythmogenic cardiomyopathy: classic desmosomal ARVC and a RIT1-related phenocopy.

Case Report: Contrasting phenotypes of arrhythmogenic cardiomyopathy: classic desmosomal ARVC and a RIT1-related phenocopy.

Journal: Frontiers in cardiovascular medicine
Published: January 13, 2026

Chemotherapy-Induced Arrhythmogenic Right Ventricular Cardiomyopathy.

Chemotherapy-Induced Arrhythmogenic Right Ventricular Cardiomyopathy.

Journal: JACC. Case reports
Published: October 31, 2025

Genetic and Clinical Characterization of FLNC Variants in Chinese Patients with Cardiomyopathy.

Genetic and Clinical Characterization of FLNC Variants in Chinese Patients with Cardiomyopathy.

Journal: Journal of cardiovascular development and disease
Published: October 17, 2025

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

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
Showing 1-12 of 170

Last Updated: 04/28/2026