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Results 1 - 10 of 37 for Familial hypertrophic cardiomyopathy 16
  1. ... HYPERTROPHIC, 9; CMH9 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 21; CMH21 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16; CMH16 PubMed Bashyam MD, Savithri GR, Kumar MS, ...
  2. ... j.yjmcc.2010.03.005. Epub 2010 Mar 16. Citation on PubMed
  3. ... JD. Update 2011: clinical and genetic issues in familial dilated cardiomyopathy. J Am Coll Cardiol. 2011 Apr 19;57(16):1641-9. doi: 10.1016/j.jacc.2011. ...
  4. ... WJ. Clinical expression of plakophilin-2 mutations in familial arrhythmogenic right ventricular cardiomyopathy. Circulation. 2006 Jan 24;113(3):356-64. doi: 10.1161/CIRCULATIONAHA.105.561654. Epub 2006 Jan 16. Citation on PubMed van Tintelen JP, Entius MM, ...
  5. ... S, Gomes AV. Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes. J Mol Cell Cardiol. 2010 May;48(5):899-909. doi: 10.1016/j.yjmcc.2010.03.005. Epub 2010 Mar 16. Citation on PubMed
  6. ... in sarcoglycanopathies. Eur J Hum Genet. 2008 Jul;16(7):793-803. doi: ... and sporadic dilated cardiomyopathy. J Clin Invest. 2000 Sep;106(5):655- ...
  7. ... Mol Genet. 2010 Oct 15;19(20):4007-16. doi: 10.1093/hmg/ddq315. Epub 2010 Jul ... idiopathic dilated cardiomyopathy. Circ Cardiovasc Genet. 2010 Apr;3(2):155- ...
  8. ... torsades de pointes. Circulation. 2002 Apr 23;105(16):1943-8. doi: ... Epub 2016 Feb 23. Citation on PubMed
  9. ... underlie catecholaminergic polymorphic ventricular tachycardia. Circulation. 2001 ... right ventricular cardiomyopathy type 2 (ARVD2). Hum Mol Genet. 2001 Feb ...
  10. ... do mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3): ... on PubMed Rodriguez JE, McCudden CR, Willis MS. Familial hypertrophic cardiomyopathy: basic concepts and future molecular diagnostics. Clin Biochem. ...
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