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Results 1 - 10 of 78 for Hypertrophic cardiomyopathy 20
  1. ... HYPERTROPHIC, 17; CMH17 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18; CMH18 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20; CMH20 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9; CMH9 CARDIOMYOPATHY, FAMILIAL ...
  2. ... expanding phenotype. Dystrophin abnormalities in X-linked dilated cardiomyopathy. Circulation. 1997 May 20;95(10):2344-7. doi: 10.1161/01. ... explains the pathogenesis of 5' X-linked dilated cardiomyopathy. BMC Med Genet. 2012 Mar 28;13:20. doi: 10.1186/1471-2350-13-20. Citation ...
  3. ... explains the pathogenesis of 5' X-linked dilated cardiomyopathy. BMC Med Genet. 2012 Mar 28;13:20. doi: 10.1186/1471-2350-13-20. Citation ...
  4. ... Increased alpha2 subunit-associated AMPK activity and PRKAG2 cardiomyopathy. Circulation. 2005 Nov 15;112(20):3140-8. doi: 10.1161/CIRCULATIONAHA.105.550806. ...
  5. ... nucleotide translocator is associated with mitochondrial myopathy and cardiomyopathy. Hum Mol Genet. 2005 Oct 15;14(20):3079-88. doi: 10.1093/hmg/ddi341. Epub ...
  6. ... Citation on PubMed Mogensen J, Arbustini E. Restrictive cardiomyopathy. Curr Opin Cardiol. 2009 May;24(3):214-20. doi: 10.1097/hco.0b013e32832a1d2e. No abstract available. ...
  7. ... single evolutionary origin as a risk factor for cardiomyopathy. Am J Hum Genet. 2000 Dec;67(6):1617-20. doi: 10.1086/316896. Epub 2000 Oct 18. ...
  8. ... Novel mutations in sarcomeric protein genes in dilated cardiomyopathy. Biochem Biophys Res Commun. 2002 Oct 18;298(1):116-20. doi: 10.1016/s0006-291x(02)02374-4. ...
  9. ... Mutations in one gene, TTN, account for approximately 20 percent of cases of familial dilated cardiomyopathy. The TTN gene provides instructions for making a ...
  10. ... doi: 10.1093/eurjhf/hfs119. Epub 2012 Jul 20. Citation on PubMed or Free article on PubMed Central
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