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The Utility of Numeric Grading Scales of Middle Ear Risk in Predicting Ossiculoplasty Hearing Outcomes.
TES-1/Tes and ZYX-1/Zyxin protect junctional actin networks under tension during epidermal morphogenesis in the C. elegans embryo.
In vitro studies on the selective cytotoxic effect of crocetin and quercetin.
Linking genotype to phenotype using the Arabidopsis unimutant collection.
Erythema ab igne in pediatric patients remote schooling during the COVID-19 pandemic: A case series.
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MR Imaging of arrhythmogenic right ventricular cardiomyopathy: morphologic findings and interobserver reliability.
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Value of 3D echocardiography in the diagnosis of arrhythmogenic right ventricular cardiomyopathy.
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Cine-computed tomography of arrhythmogenic right ventricular dysplasia.
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Arrhythmogenic Right Ventricular Dysplasia
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Ablation of ventricular arrhythmias in arrhythmogenic right ventricular dysplasia/cardiomyopathy: arrhythmia-free survival after endo-epicardial substrate based mapping and ablation.
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Outcomes of Catheter Ablation in Arrhythmogenic Right Ventricular Cardiomyopathy Without Background Implantable Cardioverter Defibrillator Therapy: A Multicenter International Ventricular Tachycardia Registry.
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Spatial and transmural properties of the reentrant ventricular tachycardia circuit in arrhythmogenic right ventricular cardiomyopathy: Simultaneous epicardial and endocardial recordings.
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A Brief Review and Update of the Clinicopathologic Diagnosis of Arrhythmogenic Cardiomyopathy.
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Characterization of the arrhythmogenic substrate in ischemic and nonischemic cardiomyopathy implications for catheter ablation of hemodynamically unstable ventricular tachycardia.
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Genetic and epigenetic regulation of arrhythmogenic cardiomyopathy.
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Homozygous founder mutation in desmocollin-2 (DSC2) causes arrhythmogenic cardiomyopathy in the Hutterite population.
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Addetia, Karima
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Lang, Roberto M.
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Kim, Gene H.
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Husain, Aliya
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