Found: 7
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Cardiac MRI assessed left ventricular hypertrophy in differentiating hypertensive heart disease from hypertrophic cardiomyopathy attributable to a sarcomeric gene mutation.
- Published in:
- 2011
- By:
- Publication type:
- journal article
The Metabolome in Finnish Carriers of the MYBPC3-Q1061X Mutation for Hypertrophic Cardiomyopathy.
- Published in:
- PLoS ONE, 2015, v. 10, n. 8, p. 1, doi. 10.1371/journal.pone.0134184
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- Publication type:
- Article
Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland.
- Published in:
- Journal of Molecular Medicine, 2002, v. 80, n. 7, p. 412, doi. 10.1007/s00109-002-0323-9
- By:
- Publication type:
- Article
Genetic basis and outcome in a nationwide study of Finnish patients with hypertrophic cardiomyopathy.
- Published in:
- ESC Heart Failure, 2019, v. 6, n. 2, p. 436, doi. 10.1002/ehf2.12420
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- Publication type:
- Article
Fibrosis and wall thickness affect ventricular repolarization dynamics in hypertrophic cardiomyopathy.
- Published in:
- 2018
- By:
- Publication type:
- journal article
CMR derived left ventricular septal convexity in carriers of the hypertrophic cardiomyopathy-causing MYBPC3-Q1061X mutation.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-42376-7
- By:
- Publication type:
- Article
Two novel mutations in the β-myosin heavy chain gene associated with dilated cardiomyopathy
- Published in:
- European Journal of Heart Failure, 2004, v. 6, n. 7, p. 861, doi. 10.1016/j.ejheart.2004.04.017
- By:
- Publication type:
- Article