Prolonged Right Ventricular Ejection Delay in Brugada Syndrome Depends on the Type of <i>SCN5A</i> Variant　― Electromechanical Coupling Through Tissue Velocity Imaging as a Bridge Between Genotyping and Phenotyping ―-Reference-Cited by-同舟云学术

Prolonged Right Ventricular Ejection Delay in Brugada Syndrome Depends on the Type of SCN5A Variant　― Electromechanical Coupling Through Tissue Velocity Imaging as a Bridge Between Genotyping and Phenotyping ―

Published:2018 Issue:1 Volume:82 Page:53-61
ISSN:1346-9843
Container-title:Circulation Journal
language:en
Short-container-title:Circ J

Author:

Van Malderen Sophie C.H.¹²³,Daneels Dorien⁴,Kerkhove Dirk⁵,Peeters Uschi⁴,Theuns Dominic A.M.J.³,Droogmans Steven⁵,Van Camp Guy⁵,Weytjens Caroline⁵,Biervliet Martine⁴,Bonduelle Maryse⁴,Van Dooren Sonia⁴,Brugada Pedro¹

Affiliation:

1. Department of Electrophysiology (Heart Rhythm Management Centre), Vrije Universiteit Brussel, UZ Brussel

2. Department of Cardiology, AZ Nikolaas

3. Department of Electrophysiology, Thorax Centre, Erasmus MC

4. Centre for Medical Genetics, Reproduction and Genetics, Reproduction Genetics and Regenerative Medicine, Vrije Universiteit Brussel, UZ Brussel

5. Department of Non-invasive Cardiology, Vrije Universiteit Brussel, UZ Brussel

Publisher

Japanese Circulation Society

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Link

https://www.jstage.jst.go.jp/article/circj/82/1/82_CJ-16-1279/_pdf

Reference45 articles.

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2. 2. Antzelevitch C, Brugada P, Borggrefe M, Brugada J, Brugada R, Corrado D, et al. Brugada syndrome: Report of the second consensus conference: Endorsed by the Heart Rhythm Society and the European Heart Rhythm Association. Circulation 2005; 111: 659–670.

3. 3. Priori SG, Wilde A, Horie M, Cho Y, Behr ER, Berul C, et al. Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes. Europace 2013; 15: 1389–1406.

4. 4. Nielsen MW, Holst AG, Olesen SP, Olesen MS. The genetic component of Brugada syndrome. Front Physiol 2013; 4: 179.

5. 5. Hu D, Barajas-Martínez H, Pfeiffer R, Dezi F, Pfeiffer J, Buch T, et al. Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome. JACC 2014; 64: 66–79.

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