Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure.
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Loss of Function Mutations in NNT Are Associated With Left Ventricular NoncompactionGenotype-phenotype associations in dilated cardiomyopathy: meta-analysis on more than 8000 individuals.CardioNet: a human metabolic network suited for the study of cardiomyocyte metabolismCardiac myosin binding protein-C: a novel sarcomeric target for gene therapyThe impact of coronary artery disease risk loci on ischemic heart failure severity and prognosis: association analysis in the COntrolled ROsuvastatin multiNAtional trial in heart failure (CORONA).Novel mutations in the sarcomeric protein myopalladin in patients with dilated cardiomyopathy.Clinical trials update from the European Society of Cardiology Meeting 2011: ARISTOTLE, SMART-AV: QLV substudy, SHIFT: echocardiography and quality of life substudies, European CRT Survey, and Basic Science Update.Developments in heart failure 2011.Polymorphisms in genes encoding nonsarcomeric proteins and their role in the pathogenesis of dilated cardiomyopathy.Hypertrophic cardiomyopathy: how do mutations lead to disease?Etiology-specific assessment of predictors of long-term survival in chronic systolic heart failureAnalysis of urinary methylated nucleosides of patients with coronary artery disease by high-performance liquid chromatography/electrospray ionization tandem mass spectrometry.Aggregate penetrance of genomic variants for actionable disorders in European and African Americans.Hypertrophic cardiomyopathy and the myosin mesa: viewing an old disease in a new light.Abnormal Mitral Valve Dimensions in Pediatric Patients with Hypertrophic Cardiomyopathy.[Competence Network Heart Failure (CNHF). Together against heart failure].Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy.Lessons from a tarantula: new insights into myosin interacting-heads motif evolution and its implications on disease.Clinical outcomes associated with sarcomere mutations in hypertrophic cardiomyopathy: a meta-analysis on 7675 individuals.Utility of next generation sequencing in genetic diagnosis of early onset neuromuscular disorders.Serum levels of microRNAs in patients with heart failure.Association of cardiac myosin-binding protein-C with the ryanodine receptor channel - putative retrograde regulation?
P2860
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P2860
Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure.
description
2011 nî lūn-bûn
@nan
2011年の論文
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2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
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name
Novel correlations between the ...... petence Network Heart Failure.
@en
Novel correlations between the ...... petence Network Heart Failure.
@nl
type
label
Novel correlations between the ...... petence Network Heart Failure.
@en
Novel correlations between the ...... petence Network Heart Failure.
@nl
prefLabel
Novel correlations between the ...... petence Network Heart Failure.
@en
Novel correlations between the ...... petence Network Heart Failure.
@nl
P2093
P2860
P50
P356
P1476
Novel correlations between the ...... petence Network Heart Failure.
@en
P2093
Anastassia Dermintzoglou
Andreas Perrot
Beate Jurmann
Bernd Timmermann
Bernhard Maisch
Cemil Özcelik
Christian Geier
German Competence Network Heart Failure
Götz Gelbrich
Hendrik Milting
P2860
P304
P356
10.1093/EURJHF/HFR074
P50
P577
2011-07-12T00:00:00Z