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ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5 (disorder)

Known as: ARVC5, Arrhythmogenic Right Ventricular Dysplasia, Familial, 5, ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 5 
National Institutes of Health

Related topics

Related topics

6 relations

Broader (1)

Arrhythmogenic Right Ventricular Dysplasia
Autosomal dominant inheritanceLeft Ventricular HypertrophyPaired ventricular premature complexesPremature ventricular contractions

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
TMEM43-S358L mutation enhances NF-κB-TGFβ signal cascade in arrhythmogenic right ventricular dysplasia/cardiomyopathy
Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is a genetic cardiac muscle disease that accounts for… 
2017
2017
Predictive Genotype Testing in Pediatric Healthy Phenotypes with Family History of ARVC-5: Initiation of Early Detection, Future Therapeutic Strategies, or Just Scaring?
Objectives: Autosomal dominant TMEM43-p.S358L mutation encoding for the ER-protein LUMA is a highly malignant fully penetrant… 
2013
2013
Long-term prognostic value of preprocedural adiponectin levels in patients undergoing percutaneous coronary intervention.
2011
2011
Mutationsanalyse an 14 Kandidatengenen für autosomal-dominant vererbte arrhythmogene rechtsventrikuläre Kardiomyopathie (ARVD5)
2009
2009
The clinical and genetic epidemiology of arrhythmogenic right ventricular cardiomyopathy in Newfoundland
Background -- Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a cause of sudden cardiac death (SCD) in young people due… 
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