(Q33165969)

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

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18 February 2020

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

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18 February 2020

arrhythmogenic right ventricular cardiomyopathy

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Alessandro Zorzi

1

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18 February 2020

Domenico Corrado

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18 February 2020

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Gaetano Thiene

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18 February 2020

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Barbara Bauce

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18 February 2020

Martina Perazzolo Marra

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Martina Perazzolo Marra

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18 February 2020

Kalliopi Pilichou

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Kalliopi Pilichou

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18 February 2020

10

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Sabino Iliceto

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18 February 2020

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Ilaria Rigato

2

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18 February 2020

Federico Migliore

5

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18 February 2020

Elisa Mazzotti

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18 February 2020

Dario Gregori

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18 February 2020

Luciano Daliento

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18 February 2020

Alessandra Rampazzo

11

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18 February 2020

Cristina Basso

12

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18 February 2020

publication date

2 July 2015

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18 February 2020

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18 February 2020

18

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18 February 2020

7

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18 February 2020

1086-1094

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18 February 2020

Molecular biology and clinical management of arrhythmogenic right ventricular cardiomyopathy/dysplasia.

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUV205

21 January 2018

Clinical management of arrhythmogenic right ventricular cardiomyopathy: an update

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUV205

21 January 2018

Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUV205

21 January 2018

Missense mutations in plakophilin-2 cause sodium current deficit and associate with a Brugada syndrome phenotype

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUV205

21 January 2018

Connexin43 and the regulation of intercalated disc function

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUV205

21 January 2018

Electrophysiological abnormalities precede overt structural changes in arrhythmogenic right ventricular cardiomyopathy due to mutations in desmoplakin-A combined murine and human study.

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUV205

21 January 2018

Intercalated disc abnormalities, reduced Na(+) current density, and conduction slowing in desmoglein-2 mutant mice prior to cardiomyopathic changes

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUV205

21 January 2018

Loss of plakophilin-2 expression leads to decreased sodium current and slower conduction velocity in cultured cardiac myocytes

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUV205

21 January 2018

Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteria.

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUV205

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUV205

21 January 2018

Implantable cardioverter-defibrillator therapy for prevention of sudden death in patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia.

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUV205

21 January 2018

Prophylactic implantable defibrillator in patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia and no prior ventricular fibrillation or sustained ventricular tachycardia

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUV205

21 January 2018

Implantable cardioverter-defibrillators in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUV205

21 January 2018

Incremental value of cardiac magnetic resonance imaging in arrhythmic risk stratification of arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutation carriers.

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUV205

21 January 2018

Pathophysiology of arrhythmogenic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUV205

21 January 2018

Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUV205

21 January 2018

Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUV205

21 January 2018

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUV205

21 January 2018

Remodeling of myocyte gap junctions in arrhythmogenic right ventricular cardiomyopathy due to a deletion in plakoglobin (Naxos disease)

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUV205

21 January 2018

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