(Q54114284)

24 May 2018

title

Arrhythmogenic right ventricular cardiomyopathy: implications of next-generation sequencing in appropriate diagnosis. (English)

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24 May 2018

arrhythmogenic right ventricular cardiomyopathy

main subject

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author

Argelia Medeiros-domingo

1

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24 May 2018

Firat Duru

object named as

Firat Duru

7

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author name string

Ardan M Saguner

2

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24 May 2018

István Magyar

3

1 reference

24 May 2018

Angela Bahr

4

1 reference

24 May 2018

Deniz Akdis

5

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24 May 2018

Corinna Brunckhorst

6

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24 May 2018

Wolfgang Berger

8

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24 May 2018

publication date

1 June 2017

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24 May 2018

published in

EP Europace

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24 May 2018

volume

19

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24 May 2018

issue

6

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24 May 2018

page(s)

1063-1069

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24 May 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).

cites work

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21 January 2018

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

21 January 2018

1 reference

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Molecular genetics of arrhythmogenic right ventricular cardiomyopathy: emerging horizon?

21 January 2018

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Genetics of arrhythmogenic right ventricular cardiomyopathy: a practical guide for physicians

21 January 2018

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Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family Members

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Atlas of the clinical genetics of human dilated cardiomyopathy

21 January 2018

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Rapid detection of genetic variants in hypertrophic cardiomyopathy by custom DNA resequencing array in clinical practice

21 January 2018

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First FDA authorization for next-generation sequencer

21 January 2018

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A genetic variants database for arrhythmogenic right ventricular dysplasia/cardiomyopathy

21 January 2018

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Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy

21 January 2018

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Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function of Nav1.5.

21 January 2018

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Loss-of-function mutation of the SCN3B-encoded sodium channel {beta}3 subunit associated with a case of idiopathic ventricular fibrillation

21 January 2018

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Sodium channel mutations and susceptibility to heart failure and atrial fibrillation

21 January 2018

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Desmosomes and the sodium channel complex: implications for arrhythmogenic cardiomyopathy and Brugada syndrome

21 January 2018

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Diagnostic dilemmas: overlapping features of brugada syndrome and arrhythmogenic right ventricular cardiomyopathy

21 January 2018

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Right bundle branch block, right precordial st-segment elevation, and sudden death in young people

21 January 2018

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Titin mutations: the fall of Goliath.

21 January 2018

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Truncations of titin causing dilated cardiomyopathy.

21 January 2018

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21 January 2018

Identifiers

DOI

10.1093/EUROPACE/EUW098

1 reference

24 May 2018

1 reference

24 May 2018