Results 1 -
10
of
99
for
Hypertrophic cardiomyopathy 3
- ... Registry: Cardiomyopathy, familial restrictive, 1 Genetic Testing Registry: Cardiomyopathy, familial restrictive, 3 National Organization for Rare Disorders (NORD) ClinicalTrials.gov ...
- ... NORD) ClinicalTrials.gov CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 2; CMH2 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3; CMH3 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4; CMH4 CARDIOMYOPATHY, FAMILIAL ...
- ... 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- ...
- ... from 312 patients with familial or idiopathic dilated cardiomyopathy. Circ Cardiovasc Genet. 2010 Apr;3(2):155-61. doi: 10.1161/CIRCGENETICS.109. ...
- ... 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, ...
- ... 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- ...
- ... plakophilin-2 mutations in familial arrhythmogenic right ventricular cardiomyopathy. Circulation. 2006 Jan 24;113(3):356-64. doi: 10.1161/CIRCULATIONAHA.105.561654. ...
- ... 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- ...
- ... 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- ...
- ... Desmoplakin mutations with palmoplantar keratoderma, woolly hair and cardiomyopathy. Acta Derm Venereol. 2015 Mar;95(3):337-40. doi: 10.2340/00015555-1974. Citation ...