Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience
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Genetics and disease of ventricular muscle.Genotype-phenotype associations in dilated cardiomyopathy: meta-analysis on more than 8000 individuals.Correction of human phospholamban R14del mutation associated with cardiomyopathy using targeted nucleases and combination therapy.Unclassifiable arrhythmic cardiomyopathy associated with Emery-Dreifuss caused by a mutation in FHL1.Familial dilated cardiomyopathy diagnosis is commonly overlooked at the time of transplant listing.Genotype-specific pathogenic effects in human dilated cardiomyopathy.Potential genetic predisposition for anthracycline-associated cardiomyopathy in families with dilated cardiomyopathy.A group approach to genetic counselling of cardiomyopathy patients: satisfaction and psychological outcomes sufficient for further implementation.Targeted sequence capture and GS-FLX Titanium sequencing of 23 hypertrophic and dilated cardiomyopathy genes: implementation into diagnostics.A1180V of cardiac sodium channel gene (SCN5A): is it a risk factor for dilated cardiomyopathy or just a common variant in Han Chinese?Genetic testing for inherited cardiac disease.A comparison of genetic findings in sudden cardiac death victims and cardiac patients: the importance of phenotypic classification.Defining phenotypes and disease progression in sarcomeric cardiomyopathies: contemporary role of clinical investigations.Proposal for a revised definition of dilated cardiomyopathy, hypokinetic non-dilated cardiomyopathy, and its implications for clinical practice: a position statement of the ESC working group on myocardial and pericardial diseases.Cardiovascular genetics: technological advancements and applicability for dilated cardiomyopathyGenetics of hypertrophic cardiomyopathy: A review of current state.Redefining the role of biomarkers in heart failure trials: expert consensus document.Truncating titin mutations are associated with a mild and treatable form of dilated cardiomyopathy.Phenotype-driven molecular autopsy for sudden cardiac death.Novel linkage of LMNA Single Nucleotide Polymorphism with Dilated Cardiomyopathy in an Indian case study.Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy.Dilated cardiomyopathy with severe arrhythmias in Emery-Dreifuss muscular dystrophy: from ablation to heart transplantation.High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutation.Cardiomyocyte Hypocontractility and Reduced Myofibril Density in End-Stage Pediatric Cardiomyopathy.Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development.Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathy.T2 mapping cardiovascular magnetic resonance identifies the presence of myocardial inflammation in patients with dilated cardiomyopathy as compared to endomyocardial biopsy.Reappraisal of the genetic diversity and pharmacogenetic assessment of CES1.Lamin A/C mutations in patients with dilated cardiomyopathy.Dilated Cardiomyopathy: Genetic Determinants and Mechanisms.Follow-up care by a genetic counsellor for relatives at risk for cardiomyopathies is cost-saving and well-appreciated: a randomised comparison.The EJHF last Editor's legacy: how can a high impact factor be built?Genomic correction of familial cardiomyopathy in human engineered cardiac tissues.Post-mortem whole-exome analysis in a large sudden infant death syndrome cohort with a focus on cardiovascular and metabolic genetic diseases.Functional implications of a rare variant in the sodium channel β1B subunit (SCN1B) in a 5-month-old male sudden infant death syndrome case.Molecular insights into cardiomyopathies associated with desmin (DES) mutationsGenetic mutation of familial dilated cardiomyopathy based on next‑generation semiconductor sequencing
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Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience
description
article
@en
im Januar 2013 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в червні 2013
@uk
name
Genetic analysis in 418 index ...... erview of 10 years' experience
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Genetic analysis in 418 index ...... erview of 10 years' experience
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type
label
Genetic analysis in 418 index ...... erview of 10 years' experience
@en
Genetic analysis in 418 index ...... erview of 10 years' experience
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prefLabel
Genetic analysis in 418 index ...... erview of 10 years' experience
@en
Genetic analysis in 418 index ...... erview of 10 years' experience
@nl
P2093
P2860
P356
P1476
Genetic analysis in 418 index ...... erview of 10 years' experience
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P2093
Anneke M van Mil
Imke Christiaans
Ingrid A W van Rijsingen
Irene M van Langen
J Peter van Tintelen
Jan D H Jongbloed
Jan G Post
Karin Y van Spaendonck-Zwarts
Maarten P van den Berg
Ronald H Lekanne Deprez
P2860
P304
P356
10.1093/EURJHF/HFT013
P577
2013-01-24T00:00:00Z