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- W2780741330 abstract "Dilated cardiomyopathy (DCM) represents a particular aetiology of systolic heart failure that frequently has a genetic background and usually affects young patients with few co-morbidities. The prognosis of DCM has improved substantially during the last decades due to more accurate aetiological characterization, the red-flag integrated approach to the disease, early diagnosis through systematic familial screening, and the concept of DCM as a dynamic disease requiring constant optimization of medical and non-pharmacological evidence-based treatments. However, some important issues in clinical management remain unresolved, including the role of cardiac magnetic resonance for diagnosis and risk categorization and the interaction between genotype and clinical phenotype, and arrhythmic risk stratification. This review offers a comprehensive survey of these and other emerging issues in the clinical management of DCM, providing where possible practical recommendations." @default.
- W2780741330 created "2018-01-05" @default.
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- W2780741330 date "2017-12-22" @default.
- W2780741330 modified "2023-10-14" @default.
- W2780741330 title "Evolving concepts in dilated cardiomyopathy" @default.
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- W2780741330 doi "https://doi.org/10.1002/ejhf.1103" @default.
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