Arrhythmogenic Cardiomyopathy: Mechanisms, Genetics, and Their Clinical Implications-Reference-Cited by-同舟云学术

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Arrhythmogenic Cardiomyopathy: Mechanisms, Genetics, and Their Clinical Implications

Published:2021-03-26 Issue:5 Volume:15 Page:
ISSN:1932-9520
Container-title:Current Cardiovascular Risk Reports
language:en
Short-container-title:Curr Cardiovasc Risk Rep

Author:

Reuter Chloe M.^ORCID,Dries Annika M.,Parikh Victoria N.

Funder

Boring Trust Research Award

John Taylor Babbitt Foundation

Sarnoff Cardiovascular Research Foundation

National Heart, Lung, and Blood Institute

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pharmacology

Link

http://link.springer.com/content/pdf/10.1007/s12170-021-00669-5.pdf

Reference87 articles.

1. Thiene G, Nava A, Corrado D, Rossi L, Pennelli N. Right ventricular cardiomyopathy and sudden death in young people. N Engl J Med. 1988;318:129–33.

2. Marcus FI, Fontaine GH. Right ventricular dysplasia: a report of 24 adult cases. Circulation. 1982;65:384–98.

3. McKoy G, Protonotarios N. Identification of a deletion in Plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease). Lancet. 2000;355:2119–24.

4. Carvajal-Huerta L. Epidermolytic palmoplantar keratoderma with woolly hair and dilated cardiomyopathy. J Am Acad Dermatol. 1998;39:418–21.

5. Corrado D, Basso C. Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: a multicenter study. J Am Coll Cardiol. 1997;30:1512–20.

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3. The Challenges of Diagnosis and Treatment of Arrhythmogenic Cardiomyopathy: Are We there yet?;Reviews in Cardiovascular Medicine;2022-08-15

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