Compound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene-related arrhythmogenic right ventricular cardiomyopathy
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Arrhythmogenic cardiomyopathyTreatment of arrhythmogenic right ventricular cardiomyopathy/dysplasia: an international task force consensus statementTreatment of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: An International Task Force Consensus StatementArrhythmogenic ventricular cardiomyopathy: A paradigm shift from right to biventricular diseaseArrhythmogenic right ventricular dysplasia/cardiomyopathy type 1: a light on molecular mechanismsArrhythmogenic Right Ventricular Dysplasia in Neuromuscular Disorders2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: The Task Force for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death of theThe ARVD/C genetic variants database: 2014 updatePhenotypic expression is a prerequisite for malignant arrhythmic events and sudden cardiac death in arrhythmogenic right ventricular cardiomyopathy.Arrhythmogenic Cardiomyopathy: Electrical and Structural PhenotypesImplantable Cardioverter-Defibrillator Therapy in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: Predictors of Appropriate Therapy, Outcomes, and Complications.Arrhythmogenic right ventricular cardiomyopathy (ARVC): cardiovascular magnetic resonance update.Arrhythmogenic cardiomyopathy in a patient with a rare loss-of-function KCNQ1 mutation.Electrocardiographic features of disease progression in arrhythmogenic right ventricular cardiomyopathy/dysplasiaThe effects of transfection reagent polyethyleneimine (PEI) and non-targeting control siRNAs on global gene expression in human aortic smooth muscle cells.Arrhythmogenic Right Ventricular Cardiomyopathy - 4 Swedish families with an associated PKP2 c.2146-1G>C variantCausality in genetics: the gradient of genetic effects and back to Koch's postulates of causality.Genotype-phenotype relationship in patients with arrhythmogenic right ventricular cardiomyopathy caused by desmosomal gene mutations: A systematic review and meta-analysis.When rare illuminates common: how cardiocutaneous syndromes transformed our perspective on arrhythmogenic cardiomyopathy.The usual suspects in sudden cardiac death of the young: a focus on inherited arrhythmogenic diseases.Genetic testing in cardiovascular diseases.Desmosomes in the heart: a review of clinical and mechanistic analyses.Arrhythmogenic cardiomyopathy: a disease of intercalated discs.Clinical interpretation of genetic variants in arrhythmogenic right ventricular cardiomyopathy.The research venture in arrhythmogenic right ventricular cardiomyopathy: a paradigm of translational medicine.Determined to Fail--the Role of Genetic Mechanisms in Heart Failure.Contribution of exome sequencing for genetic diagnostic in arrhythmogenic right ventricular cardiomyopathy/dysplasiaArrhythmogenic Right Ventricular Cardiomyopathy: Risk Stratification and Indications for Defibrillator Therapy.Molecular mechanisms in the pathogenesis of arrhythmogenic cardiomyopathy.Genetic and epigenetic regulation of arrhythmogenic cardiomyopathy.Approach to family screening in arrhythmogenic right ventricular dysplasia/cardiomyopathy.Case reports of two pedigrees with recessive arrhythmogenic right ventricular cardiomyopathy associated with homozygous Thr335Ala variant in DSG2.Nature and Nurture in Arrhythmogenic Right Ventricular Cardiomyopathy - A Clinical PerspectiveElectrocardiographic differentiation of idiopathic right ventricular outflow tract ectopy from early arrhythmogenic right ventricular cardiomyopathy.MicroRNA-130a Regulation of Desmocollin 2 in a Novel Model of Arrhythmogenic Cardiomyopathy.Unique genetic background and outcome of non-Caucasian Japanese probands with arrhythmogenic right ventricular dysplasia/cardiomyopathy.High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutation.Arrhythmogenic cardiomyopathy: pathology, genetics, and concepts in pathogenesis.Targeted next generation sequencing in a young population with suspected inherited malignant cardiac arrhythmias.Sex hormones affect outcome in arrhythmogenic right ventricular cardiomyopathy/dysplasia: from a stem cell derived cardiomyocyte-based model to clinical biomarkers of disease outcome.
P2860
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P2860
Compound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene-related arrhythmogenic right ventricular cardiomyopathy
description
2013 nî lūn-bûn
@nan
2013 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Compound and digenic heterozyg ...... ght ventricular cardiomyopathy
@ast
Compound and digenic heterozyg ...... ght ventricular cardiomyopathy
@en
Compound and digenic heterozyg ...... ght ventricular cardiomyopathy
@nl
type
label
Compound and digenic heterozyg ...... ght ventricular cardiomyopathy
@ast
Compound and digenic heterozyg ...... ght ventricular cardiomyopathy
@en
Compound and digenic heterozyg ...... ght ventricular cardiomyopathy
@nl
prefLabel
Compound and digenic heterozyg ...... ght ventricular cardiomyopathy
@ast
Compound and digenic heterozyg ...... ght ventricular cardiomyopathy
@en
Compound and digenic heterozyg ...... ght ventricular cardiomyopathy
@nl
P2093
P50
P3181
P1476
Compound and digenic heterozyg ...... ght ventricular cardiomyopathy
@en
P2093
Andrea Nava
Federico Migliore
Kalliopi Pilichou
Luciano Daliento
Sabino Iliceto
P304
P3181
P356
10.1161/CIRCGENETICS.113.000288
P407
P50
P577
2013-12-01T00:00:00Z