Prevalence and clinical phenotype of hereditary transthyretin amyloid cardiomyopathy in patients with increased left ventricular wall thickness-Reference-Cited by-同舟云学术

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Prevalence and clinical phenotype of hereditary transthyretin amyloid cardiomyopathy in patients with increased left ventricular wall thickness

Published:2015-11-03 Issue:23 Volume:37 Page:1826-1834
ISSN:0195-668X
Container-title:European Heart Journal
language:en
Short-container-title:Eur Heart J

Author:

Damy Thibaud,Costes Bruno,Hagège Albert A.,Donal Erwan,Eicher Jean-Christophe,Slama Michel,Guellich Aziz,Rappeneau Stéphane,Gueffet Jean-Pierre,Logeart Damien,Planté-Bordeneuve Violaine,Bouvaist Hélène,Huttin Olivier,Mulak Geneviève,Dubois-Randé Jean-Luc,Goossens Michel,Canoui-Poitrine Florence,Buxbaum Joel N.

Funder

French Society of Cardiology

Pfizer

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

Link

http://academic.oup.com/eurheartj/article-pdf/37/23/1826/6733717/ehv583.pdf

Reference24 articles.

1. Classification of the cardiomyopathies: a position statement from the european society of cardiology working group on myocardial and pericardial diseases

2. Genetics of Hypertrophic Cardiomyopathy After 20 Years

3. Molecular Mechanisms of Amyloidosis

4. Role of natriuretic peptide to predict cardiac abnormalities in patients with hereditary transthyretin amyloidosis

5. Variant-Sequence Transthyretin (Isoleucine 122) in Late-Onset Cardiac Amyloidosis in Black Americans

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4. Mechanisms of damage and therapies for cardiac amyloidosis: a role for inflammation?;Clinical Research in Cardiology;2024-08-21

5. Health-related quality of life is an independent predictor of mortality and hospitalisations in transthyretin amyloid cardiomyopathy: a prospective cohort study;Quality of Life Research;2024-08-06

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