Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy.
about
The biochemical and mass spectrometric profiling of the dystrophin complexome from skeletal muscleDisease rescue and increased lifespan in a model of cardiomyopathy and muscular dystrophy by combined AAV treatmentsRare variant mutations identified in pediatric patients with dilated cardiomyopathyProteomic analysis reveals new cardiac-specific dystrophin-associated proteinsCanine candidate genes for dilated cardiomyopathy: annotation of and polymorphic markers for 14 genes.The absence of dystrophin brain isoform expression in healthy human heart ventricles explains the pathogenesis of 5' X-linked dilated cardiomyopathy.A defect in dystrophin causes a novel porcine stress syndrome.Challenges and opportunities in dystrophin-deficient cardiomyopathy gene therapy.Progress in gene therapy of dystrophic heart disease.Exclusive skeletal muscle correction does not modulate dystrophic heart disease in the aged mdx model of Duchenne cardiomyopathyCardiac expression of a mini-dystrophin that normalizes skeletal muscle force only partially restores heart function in aged Mdx mice.Molecular basis of hereditary cardiomyopathy: abnormalities in calcium sensitivity, stretch response, stress response and beyond.Genetics in dilated cardiomyopathy.Heart failure in younger patients: the Meta-analysis Global Group in Chronic Heart Failure (MAGGIC).Pathoproteomic profiling of the skeletal muscle matrisome in dystrophinopathy associated myofibrosis.Dystrophin genotype-cardiac phenotype correlations in Duchenne and Becker muscular dystrophies using cardiac magnetic resonance imaging.Genomic Insights into Cardiomyopathies: A Comparative Cross-Species Review.Clinical Manifestations and Overall Management Strategies for Duchenne Muscular Dystrophy.Multiple Species Comparison of Cardiac Troponin T and Dystrophin: Unravelling the DNA behind Dilated Cardiomyopathy.Myocardial Fibrosis and Left Ventricular Dysfunction in Duchenne Muscular Dystrophy Carriers Using Cardiac Magnetic Resonance Imaging.Dystrophic Cardiomyopathy: Complex Pathobiological Processes to Generate Clinical Phenotype.Cardiac involvement in female Duchenne and Becker muscular dystrophy carriers in comparison to their first-degree male relatives: a comparative cardiovascular magnetic resonance study.X-Linked Dilated Cardiomyopathy Presenting as Acute Rhabdomyolysis and Presumed Epstein-Barr Virus-Induced Viral Myocarditis: A Case Report.A novel DMD splicing mutation found in a family responsible for X-linked dilated cardiomyopathy with hyper-CKemia.
P2860
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P2860
Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy.
@ast
Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy.
@en
type
label
Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy.
@ast
Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy.
@en
prefLabel
Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy.
@ast
Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy.
@en
P2860
P356
P1433
P1476
Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy.
@en
P2093
P2860
P304
P356
10.1136/HRT.2003.023390
P407
P577
2004-08-01T00:00:00Z