MOGE(S): a standardized classification of cardiomyopathies?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine
Link
http://www.nature.com/articles/nrcardio.2013.219.pdf
Reference10 articles.
1. Arbustini, E. et al. The MOGE(S) classification for a phenotype–genotype nomenclature of cardiomyopathy: endorsed by the World Heart Federation. J. Am. Coll. Cardiol. 62, 2046–2072 (2013).
2. Watkins, D. A. & Mayosi, B. M. The contribution of South Africans to the subject of dilated cardiomyopathy. Cardiovasc. J. Afr. 20, 11–16 (2009).
3. Report of the WHO/ISFC Task Force on the Definition and Classification of Cardiomyopathies. Br. Heart J. 44, 672–673 (1980).
4. 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).
5. Maron, B. J. et al. 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).
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1. Clinical Reasoning and Classification of Cardiomyopathies;ABC: Heart Failure & Cardiomyopathy;2023
2. Complex roads from genotype to phenotype in dilated cardiomyopathy: scientific update from the Working Group of Myocardial Function of the European Society of Cardiology;Cardiovascular Research;2018-05-23
3. The MOGE(S) classification for cardiomyopathies: current status and future outlook;Heart Failure Reviews;2017-07-19
4. Clinical Application of WHF-MOGE(S) Classification for Hypertrophic Cardiomyopathy;Global Heart;2015-09-01
5. The MOGE(S) Classification of Cardiomyopathy for Clinicians;Journal of the American College of Cardiology;2014-07
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