Dilated cardiomyopathy-Reference-Cited by-同舟云学术

Dilated cardiomyopathy

Published:2019-05-09 Issue:1 Volume:5 Page:
ISSN:2056-676X
Container-title:Nature Reviews Disease Primers
language:en
Short-container-title:Nat Rev Dis Primers

Author:

Schultheiss Heinz-Peter,Fairweather DeLisa,Caforio Alida L. P.,Escher Felicitas,Hershberger Ray E.,Lipshultz Steven E.,Liu Peter P.,Matsumori Akira,Mazzanti Andrea,McMurray John,Priori Silvia G.

Publisher

Springer Science and Business Media LLC

Subject

General Medicine

Link

http://www.nature.com/articles/s41572-019-0084-1.pdf

Reference255 articles.

1. Hershberger, R. E., Morales, A. & Siegfried, J. D. Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionals. Genet. Med. 12, 655–667 (2010). This review article provides a wide and detailed overview of clinical and genetic issues in specific types of genetic DCM.

2. McKenna, W. J., Maron, B. J. & Thiene, G. Classification, epidemiology, and global burden of cardiomyopathies. Circ. Res. 121, 722–730 (2017).

3. Maron, B. J. Contemporary definitions and classification of the cardiomyopathies: an American Heart Association scientific statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; and Council on Epidemiology and Prevention. Circulation 113, 1807–1816 (2006).

4. Elliott, P. et al. Classification of the cardiomyopathies: a position statement from the european society of cardiology working group on myocardial and pericardial diseases. Eur. Heart J. 29, 270–276 (2007).

5. Richardson, P. et al. Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the definition and classification of cardiomyopathies. Circulation 93, 841–842 (1996).

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