Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC/D): A Systematic Literature Review - Wikidata - wikimedia - TriplyDB

Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC/D): A Systematic Literature Review

Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC/D): A Systematic Literature Review

http://www.wikidata.org/entity/Q36887235

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Role of Imaging Techniques for Diagnosis, Prognosis and Management of Heart Failure Patients: Cardiac Magnetic Resonance.Regional differences in WT-1 and Tcf21 expression during ventricular development: implications for myocardial compaction Embodying a New Meaning of Being At Risk: Living With an Implantable Cardioverter Defibrillator for Arrhythmogenic Right Ventricular Cardiomyopathy.Remodeling of cell-cell junctions in arrhythmogenic cardiomyopathy Cell models of arrhythmogenic cardiomyopathy: advances and opportunities.A meta-analysis for echocardiographic assessment of right ventricular structure and function in ARVC Cardiac sarcoidosis mimicking arrhythmogenic right ventricular dysplasia in a patient presenting with monomorphic ventricular tachycardia Rapidly formed right ventricular thrombus detected by intracardiac echocardiography before catheter ablation in a case of arrhythmogenic right ventricular cardiomyopathy.First Reported Case of Arrhythmogenic Right Ventricular Cardiomyopathy in Oman.Surgical Treatment of Arrhythmogenic Right Ventricular Cardiomyopathy with Absent Pulmonary Valve.Massively Parallel Sequencing of Genes Implicated in Heritable Cardiac Disorders: A Strategy for a Small Diagnostic Laboratory.Isolated Cardiac Sarcoidosis Mimicking Arrhythmogenic Right Ventricular Cardiomyopathy.Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) in clinical practice.

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Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC/D): A Systematic Literature Review

http://www.wikidata.org/entity/Q36887235

description

2013 nî lūn-bûn

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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2013年论文

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2013年论文

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Clinical Medicine Insights. Cardiology

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Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC/D): A Systematic Literature Review

@en

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Carlos Manrique

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Eliany Mejia-Lopez

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Richard Lucariello

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Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy

Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy

Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene

Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma

A previously undescribed congenital malformation of the heart: almost total absence of the myocardium of the right ventricle

A new locus for arrhythmogenic right ventricular cardiomyopathy (ARVD2) maps to chromosome 1q42-q43

Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy

Clinical expression of plakophilin-2 mutations in familial arrhythmogenic right ventricular cardiomyopathy

Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression

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97-114

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scholarly article

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10.4137/CMC.S10940

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7

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2013-05-21T00:00:00Z

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arrhythmogenic right ventricular cardiomyopathy

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3667685

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