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International Journal of Cardiology|February 16, 2019
Heart failure in patients with arrhythmogenic right ventricular cardiomyopathy: Genetic characteristicsAnnina S Vischer, Silvia Castelletti, Petros Syrris, et al.Circulation. Cardiovascular Genetics|December 7, 2011
Long-term outcomes in hypertrophic cardiomyopathy caused by mutations in the cardiac troponin T geneFerdinando Pasquale, Petros Syrris, Juan Pablo Kaski, et al.Circulation|March 21, 2007
Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expressionSrijita Sen-Chowdhry, Petros Syrris, Deirdre Ward, et al.European Journal of Human Genetics : EJHG|May 27, 2018
Frequency of genetic variants associated with arrhythmogenic right ventricular cardiomyopathy in the genome aggregation databaseCharlotte L Hall, Henry Sutanto, Chrysoula Dalageorgou, et al.American Journal of Human Genetics|October 10, 2007
A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathyAngeliki Asimaki, Petros Syrris, Thomas Wichter, et al.Circulation. Cardiovascular Genetics|June 24, 2010
Mutational heterogeneity, modifier genes, and environmental influences contribute to phenotypic diversity of arrhythmogenic cardiomyopathySrijita Sen-Chowdhry, Petros Syrris, Antonios Pantazis, et al.Journal of Cutaneous Pathology|January 31, 2009
Unique epidermolytic bullous dermatosis with associated lethal cardiomyopathy related to novel desmoplakin mutationsAngeliki Asimaki, Petros Syrris, Deirdre Ward, et al.European Journal of Medical Genetics|November 18, 2023
Cardiovascular involvement in later-onset malonyl-CoA decarboxylase deficiency: Case studies and literature reviewEmanuele Monda, Athanasios Bakalakos, Petros Syrris, et al.Bioinformatics (Oxford, England)|June 19, 2016
The structural effects of mutations can aid in differential phenotype prediction of beta-myosin heavy chain (Myosin-7) missense variantsNouf S Al-Numair, Luis Lopes, Petros Syrris, et al.European Journal of Human Genetics : EJHG|March 14, 2008
Micro-exons of the cardiac myosin binding protein C gene: flanking introns contain a disproportionately large number of hypertrophic cardiomyopathy mutationsRune Frank-Hansen, Stephen P Page, Petros Syrris, et al.Pageof 13