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Results 1 - 10 of 98 for Hypertrophic cardiomyopathy 3
  1. ... Registry: Cardiomyopathy, familial restrictive, 1 Genetic Testing Registry: Cardiomyopathy, familial restrictive, 3 National Organization for Rare Disorders (NORD) ClinicalTrials.gov ...
  2. ... NORD) ClinicalTrials.gov CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 2; CMH2 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3; CMH3 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4; CMH4 CARDIOMYOPATHY, FAMILIAL ...
  3. ... from 312 patients with familial or idiopathic dilated cardiomyopathy. Circ Cardiovasc Genet. 2010 Apr;3(2):155-61. doi: 10.1161/CIRCGENETICS.109. ... mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3):245-55. doi: 10.1007/s12265-011-9266- ...
  4. ... from 312 patients with familial or idiopathic dilated cardiomyopathy. Circ Cardiovasc Genet. 2010 Apr;3(2):155-61. doi: 10.1161/CIRCGENETICS.109. ...
  5. ... Testing Registry: 3-methylglutaconic aciduria type 5 Dilated cardiomyopathy with ataxia National Organization for Rare Disorders (NORD) ClinicalTrials.gov 3-METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5 PubMed Davey KM, ...
  6. ... mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3):245-55. doi: 10.1007/s12265-011-9266- ...
  7. ... plakophilin-2 mutations in familial arrhythmogenic right ventricular cardiomyopathy. Circulation. 2006 Jan 24;113(3):356-64. doi: 10.1161/CIRCULATIONAHA.105.561654. ...
  8. ... mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3):245-55. doi: 10.1007/s12265-011-9266- ...
  9. ... mutations in contractile proteins cause the primary familial cardiomyopathies? J Cardiovasc Transl Res. 2011 Jun;4(3):245-55. doi: 10.1007/s12265-011-9266- ...
  10. ... Desmoplakin mutations with palmoplantar keratoderma, woolly hair and cardiomyopathy. Acta Derm Venereol. 2015 Mar;95(3):337-40. doi: 10.2340/00015555-1974. Citation ...
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