Risk Stratification in Arrhythmogenic Right Ventricular Cardiomyopathy.

scientific article published in November 2017

Risk Stratification in Arrhythmogenic Right Ventricular Cardiomyopathy. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1161/CIRCULATIONAHA.117.030792
P932PMC publication ID5777304
P698PubMed publication ID29158215

P50authorDomenico CorradoQ56529119
Hugh CalkinsQ67190496
P2093author name stringFrank Marcus
P2860cites workArrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 geneQ24656100
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Incidence and predictors of implantable cardioverter-defibrillator therapy in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy undergoing implantable cardioverter-defibrillator implantation for primary preventionQ84974205
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Long-Term Outcome With Catheter Ablation of Ventricular Tachycardia in Patients With Arrhythmogenic Right Ventricular CardiomyopathyQ86644555
Potentially Lethal Ventricular Arrhythmias and Heart Failure in Arrhythmogenic Right Ventricular Cardiomyopathy: What Are the Differences Between Men and Women?Q88668354
Arrhythmogenic right ventricular cardiomyopathy 2012: diagnostic challenges and treatmentQ33161666
Predictors of appropriate ICD therapy in patients with arrhythmogenic right ventricular cardiomyopathy: long term experience of a tertiary care centerQ33161842
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Different prognostic value of functional right ventricular parameters in arrhythmogenic right ventricular cardiomyopathy/dysplasiaQ33163807
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Phenotypic expression is a prerequisite for malignant arrhythmic events and sudden cardiac death in arrhythmogenic right ventricular cardiomyopathy.Q33165969
Clinical Presentation and Outcomes by Sex in Arrhythmogenic Right Ventricular Cardiomyopathy: Findings from the North American ARVC RegistryQ33166782
Arrhythmogenic Right Ventricular Cardiomyopathy: Clinical Course and Predictors of Arrhythmic Risk.Q33167985
Long-term follow-up in patients with arrhythmogenic right ventricular diseaseQ33168115
Cardiac phenotype and long-term prognosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia patients with late presentation.Q33168279
Implantable Cardioverter-Defibrillator Therapy in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: Predictors of Appropriate Therapy, Outcomes, and ComplicationsQ33168709
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Right ventricular dysplasia: a report of 24 adult casesQ34714742
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Vigorous physical activity impairs myocardial function in patients with arrhythmogenic right ventricular cardiomyopathy and in mutation positive family members.Q34782131
Exercise has a disproportionate role in the pathogenesis of arrhythmogenic right ventricular dysplasia/cardiomyopathy in patients without desmosomal mutations.Q35115127
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Association of competitive and recreational sport participation with cardiac events in patients with arrhythmogenic right ventricular cardiomyopathy: results from the North American multidisciplinary study of arrhythmogenic right ventricular cardiomQ35847506
Task Force 8: classification of sportsQ36101187
Central role for GSK3β in the pathogenesis of arrhythmogenic cardiomyopathyQ36884231
Exercise increases age-related penetrance and arrhythmic risk in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutation carriers.Q37259910
Incremental value of cardiac magnetic resonance imaging in arrhythmic risk stratification of arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutation carriers.Q37676235
Cardiac MR findings and potential diagnostic pitfalls in patients evaluated for arrhythmogenic right ventricular cardiomyopathyQ38259638
Evaluation of Structural Progression in Arrhythmogenic Right Ventricular Dysplasia/CardiomyopathyQ39015719
Comparison of Features of Fatal Versus Nonfatal Cardiac Arrest in Patients With Arrhythmogenic Right Ventricular Dysplasia/CardiomyopathyQ40200753
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Etiology of Sudden Death in Sports: Insights From a United Kingdom Regional Registry.Q40766721
Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family MembersQ41144205
Risk Stratification in Arrhythmic Right Ventricular Cardiomyopathy Without Implantable Cardioverter-Defibrillators.Q41552188
Subcutaneous implantable cardioverter-defibrillator Post-Approval Study: Clinical characteristics and perioperative results.Q45059087
Electrocardiographic predictors of electroanatomic scar size in arrhythmogenic right ventricular cardiomyopathy: implications for arrhythmic risk stratificationQ47212075
Sex hormones affect outcome in arrhythmogenic right ventricular cardiomyopathy/dysplasia: from a stem cell derived cardiomyocyte-based model to clinical biomarkers of disease outcomeQ48251222
Risk stratification of arrhythmogenic right ventricular cardiomyopathy based on signal averaged electrocardiogramsQ48296011
Nationwide (Denmark) study of symptoms preceding sudden death due to arrhythmogenic right ventricular cardiomyopathy.Q50560818
Outcomes and ventricular tachycardia recurrence characteristics after epicardial ablation of ventricular tachycardia in arrhythmogenic right ventricular dysplasia/cardiomyopathy.Q51023298
Predictors of appropriate implantable defibrillator therapies in patients with arrhythmogenic right ventricular dysplasia.Q51329457
Implantable cardioverter-defibrillators in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy.Q51674425
Implantable cardioverter/defibrillator therapy in arrhythmogenic right ventricular cardiomyopathy: single-center experience of long-term follow-up and complications in 60 patients.Q51704331
Safety of American Heart Association-recommended minimum exercise for desmosomal mutation carriers.Q52920761
Arrhythmogenic Right Ventricular Cardiomyopathy.Q52932634
P433issue21
P407language of work or nameEnglishQ1860
P921main subjectarrhythmogenic right ventricular cardiomyopathyQ2555727
P304page(s)2068-2082
P577publication date2017-11-01
P1433published inCirculationQ578091
P1476titleRisk Stratification in Arrhythmogenic Right Ventricular Cardiomyopathy.
P478volume136

Reverse relations

cites work (P2860)
Q97648957Characteristics and prognostic implications of tricuspid regurgitation in patients with arrhythmogenic cardiomyopathy
Q92376906Clinical features and arrhythmic complications of patients with pediatric-onset arrhythmogenic right ventricular dysplasia
Q99613010Comparison of different prediction models for the indication of implanted cardioverter defibrillator in patients with arrhythmogenic right ventricular cardiomyopathy
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Q60046136Identification of Crucial Genes and Pathways in Human Arrhythmogenic Right Ventricular Cardiomyopathy by Coexpression Analysis
Q90441553Left Ventricular Involvement in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Predicts Adverse Clinical Outcomes: A Cardiovascular Magnetic Resonance Feature Tracking Study
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Q58541337PKP2 and DSG2 genetic variations in Latvian arrhythmogenic right ventricular dysplasia/cardiomyopathy registry patients
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Q95940975Plasma testosterone and arrhythmic events in male patients with arrhythmogenic right ventricular cardiomyopathy
Q90668307Relationship Between Electrocardiographic Findings and Cardiac Magnetic Resonance Phenotypes in Arrhythmogenic Cardiomyopathy
Q64230001Sudden Death and Left Ventricular Involvement in Arrhythmogenic Cardiomyopathy
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Q58578329Variants: Association With Cardiac Disorders
Q91645466Whole-Exome Sequencing Identified a De Novo Mutation of Junction Plakoglobin (p.R577C) in a Chinese Patient with Arrhythmogenic Right Ventricular Cardiomyopathy

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