Hypertrophic cardiomyopathy: diagnosis, risk stratification and treatment
- PMID: 23109605
- PMCID: PMC3563885
- DOI: 10.1503/cmaj.120138
Hypertrophic cardiomyopathy: diagnosis, risk stratification and treatment
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References
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- Jarcho JA, McKenna W, Pare JA, et al. Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1. N Engl J Med 1989;321:1372–8 - PubMed
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- Harris KM, Spirito P, Maron MS, et al. Prevalence, clinical profile, and significance of left ventricular remodeling in the end-stage phase of hypertrophic cardiomyopathy. Circulation 2006; 114:216–25 - PubMed
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- Christiaans I, Birnie E, Bonsel GJ, et al. Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: determining the best cardiological screening strategy. Eur Heart J 2011;32:1161–70 - PubMed
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