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Cited by 257

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Inherited Cardiomyopathies

Epstein, Franklin H., Kelly, Daniel P., Strauss, Arnold W.·1994·New England Journal of Medicine

Abstract

Cardiomyopathy is an important cause of morbidity and mortality throughout the world in children and adults. In contrast to secondary causes of cardiomyopathy, such as hypertension and ischemic heart disease, the causes and pathogenesis of primary myocardial disease are poorly understood. The term “idiopathic cardiomyopathy” is therefore often used to describe primary myocardial disease. The annual incidence of idiopathic dilated cardiomyopathy in the United States and Europe is estimated to range from 2 to 8 cases per 100,0001. Overall, the survival of patients with idiopathic cardiomyopathy is poor (only 50 to 60 percent at two years).Familial analyses have . . .

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Crossref · 10.1056/nejm199403313301308

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Metadata

Authors
Epstein, F. H., Kelly, D. P., & Strauss, A. W.
Venue
New England Journal of Medicine
Published
1994-03-31
Volume
330
Issue
13
Pages
913-919
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W4242169888
Cited by
257
References
2
FWCI
8.99
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Inherited Cardiomyopathies. https://app.cochat.ai/papers/10.1056/nejm199403313301308
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Epstein, F. H., Kelly, D. P., & Strauss, A. W. (1994). Inherited Cardiomyopathies. New England Journal of Medicine. https://doi.org/10.1056/nejm199403313301308

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.