The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy.
about
Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhoodHomozygosity mapping and exome sequencing reveal GATAD1 mutation in autosomal recessive dilated cardiomyopathyMany roads lead to a broken heart: the genetics of dilated cardiomyopathy.Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathyThe cell biology of disease: cellular mechanisms of cardiomyopathy.Cardiac disease and arrhythmogenesis: Mechanistic insights from mouse modelsMutational analysis of the beta- and delta-sarcoglycan genes in a large number of patients with familial and sporadic dilated cardiomyopathySodium channel mutations and susceptibility to heart failure and atrial fibrillationAutosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylationDisruption of striated preferentially expressed gene locus leads to dilated cardiomyopathy in miceA novel arginine to tryptophan (R144W) mutation in troponin T (cTnT) gene in an indian multigenerational family with dilated cardiomyopathy (FDCM)Cardiomyopathy in α-kinase 3 (ALPK3)-deficient miceShort read (next-generation) sequencing: a tutorial with cardiomyopathy diagnostics as an exemplar.Imaging phenotype vs genotype in nonhypertrophic heritable cardiomyopathies: dilated cardiomyopathy and arrhythmogenic right ventricular cardiomyopathyModeling structural and functional deficiencies of RBM20 familial dilated cardiomyopathy using human induced pluripotent stem cellsArray lessons from the heart: focus on the genome and transcriptome of cardiomyopathies.Progression from hypertrophic to dilated cardiomyopathy in mice that express a mutant myosin transgene.Cascade screening in families with inherited cardiac diseases driven by cardiologists: feasibility and nationwide outcome in long QT syndrome.Dystrophin analysis in idiopathic dilated cardiomyopathy.Familial aggregation of idiopathic dilated cardiomyopathy: clinical features and pedigree analysis in 14 families.Role of autoimmunity in dilated cardiomyopathyFamilial dilated cardiomyopathy.Familial dilated cardiomyopathy diagnosis is commonly overlooked at the time of transplant listing.Absence of linkage between idiopathic dilated cardiomyopathy and candidate genes involved in the immune function in a large Italian pedigree.Exclusion of a primary gene defect at the HLA locus in familial idiopathic dilated cardiomyopathyRbm20-deficient cardiogenesis reveals early disruption of RNA processing and sarcomere remodeling establishing a developmental etiology for dilated cardiomyopathy.The cardiomyopathies: an overviewRescue of hereditary form of dilated cardiomyopathy by rAAV-mediated somatic gene therapy: amelioration of morphological findings, sarcolemmal permeability, cardiac performances, and the prognosis of TO-2 hamsters.Circulating cardiac autoantibodies in dilated cardiomyopathy and myocarditis: pathogenetic and clinical significance.Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22.Toward an understanding of the cause of mitral valve prolapseMolecular etiology of idiopathic cardiomyopathy.Features and outcomes in utero and after birth of fetuses with myocardial diseaseTruncations of titin causing dilated cardiomyopathy.A proton leak current through the cardiac sodium channel is linked to mixed arrhythmia and the dilated cardiomyopathy phenotype.Does delta-sarcoglycan-associated autosomal-dominant cardiomyopathy exist?The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.DCM-related tropomyosin mutants E40K/E54K over-inhibit the actomyosin interaction and lead to a decrease in the number of cycling cross-bridges.Animal models of cardiac disease and stem cell therapy.Recent insights into the role of autoimmunity in idiopathic dilated cardiomyopathy.
P2860
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P2860
The frequency of familial dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年学术文章
@wuu
1992年学术文章
@zh
1992年学术文章
@zh-cn
1992年学术文章
@zh-hans
1992年学术文章
@zh-my
1992年学术文章
@zh-sg
1992年學術文章
@yue
1992年學術文章
@zh-hant
name
The frequency of familial dila ...... pathic dilated cardiomyopathy.
@en
The frequency of familial dila ...... pathic dilated cardiomyopathy.
@nl
type
label
The frequency of familial dila ...... pathic dilated cardiomyopathy.
@en
The frequency of familial dila ...... pathic dilated cardiomyopathy.
@nl
prefLabel
The frequency of familial dila ...... pathic dilated cardiomyopathy.
@en
The frequency of familial dila ...... pathic dilated cardiomyopathy.
@nl
P2093
P1476
The frequency of familial dila ...... pathic dilated cardiomyopathy.
@en
P2093
Burnett JC
Chesebro JH
Driscoll DJ
Michels VV
Rodeheffer RJ
Tazelaar HD
P356
10.1056/NEJM199201093260201
P407
P577
1992-01-01T00:00:00Z