Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy (Q24299388)

regulation of heart rate by cardiac conduction

Europe PubMed Central

title

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

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GOA release 2020-03-11

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GOA release 2020-03-11

2

Petros Syrris

Petros

Syrris

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PubMed

PubMed publication ID

30 October 2023

William J McKenna

3

William J

McKenna

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PubMed

PubMed publication ID

30 October 2023

Srijita Sen-Chowdhry

1

Srijita

Sen-Chowdhry

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PubMed

PubMed publication ID

17980246

Journal of the American College of Cardiology

30 October 2023

language of work or name

English

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publication date

6 November 2007

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published in

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volume

50

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issue

19

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page(s)

1813-21

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cites work

Recessive arrhythmogenic right ventricular dysplasia due to novel cryptic splice mutation in PKP2.

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Familial occurrence of right ventricular dysplasia: a study involving nine families

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Arrhythmogenic right ventricular cardiomyopathy: clinical presentation, diagnosis, and management

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Arrhythmogenic right ventricular dysplasia type 1 and mutations in transforming growth factor beta3 gene regulatory regions: a breakthrough?

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

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/10.1016/J.JACC.2007.08.008

7 January 2021

Arrhythmogenic right ventricular cardiomyopathy due to a novel plakophilin 2 mutation: wide spectrum of disease in mutation carriers within a family

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

The impact of implantable cardioverter-defibrillator therapy on survival in autosomal-dominant arrhythmogenic right ventricular cardiomyopathy (ARVD5)

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Penetrance of mutations in plakophilin-2 among families with arrhythmogenic right ventricular dysplasia/cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Cardiovascular Magnetic Resonance in Arrhythmogenic Right Ventricular Cardiomyopathy Revisited

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease).

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

1 reference

7 January 2021

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

1 reference

7 January 2021

Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Prospective evaluation of relatives for familial arrhythmogenic right ventricular cardiomyopathy/dysplasia reveals a need to broaden diagnostic criteria

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

A recessive mutation in desmoplakin causes arrhythmogenic right ventricular dysplasia, skin disorder, and woolly hair

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

American College of Cardiology/European Society of Cardiology clinical expert consensus document on hypertrophic cardiomyopathy. A report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents and the Euro

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: a multicenter study.

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Founder mutations among the Dutch

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Cardiac sarcoidosis masquerading as right ventricular dysplasia

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Right ventricular cardiomyopathy and sudden death in young people

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

DSG2 mutations contribute to arrhythmogenic right ventricular dysplasia/cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Desmoplakin disease in arrhythmogenic right ventricular cardiomyopathy: early genotype-phenotype studies

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Ultrastructural evidence of intercalated disc remodelling in arrhythmogenic right ventricular cardiomyopathy: an electron microscopy investigation on endomyocardial biopsies

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Desmoglein-2 mutations in arrhythmogenic right ventricular cardiomyopathy: a genotype-phenotype characterization of familial disease

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Left ventricular involvement in arrhythmogenic right ventricular cardiomyopathy - a scintigraphic and echocardiographic study.

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Genetics of right ventricular cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Loss of desmoplakin isoform I causes early onset cardiomyopathy and heart failure in a Naxos-like syndrome

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Arrhythmogenic right ventricular dysplasia/cardiomyopathy: need for an international registry. Study Group on Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy of the Working Groups on Myocardial and Pericardial Disease and Arrhythmias of th

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies.

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Desmosomal dysfunction due to mutations in desmoplakin causes arrhythmogenic right ventricular dysplasia/cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Novel mutation in desmoplakin causes arrhythmogenic left ventricular cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Clinical expression of plakophilin-2 mutations in familial arrhythmogenic right ventricular cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Role of genetic analyses in cardiology: part I: mendelian diseases: cardiac channelopathies

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Clinical features of arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in plakophilin-2

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Arrhythmogenic right ventricular cardiomyopathy/dysplasia: clinical impact of molecular genetic studies

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

Age- and Training-Dependent Development of Arrhythmogenic Right Ventricular Cardiomyopathy in Heterozygous Plakoglobin-Deficient Mice

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021

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/10.1016/J.JACC.2007.08.008

7 January 2021

Novel mutation of plakophilin-2 associated with arrhythmogenic right ventricular cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016/J.JACC.2007.08.008

7 January 2021