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Thomas Wichter

Showing results (81-90 of 92) with videos related to

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Human Molecular Genetics|April 24, 2012
Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathyFelix W Friedrich, Brendan R Wilding, Silke Reischmann, et al.
Cardiology|June 26, 2003
MR Imaging of arrhythmogenic right ventricular cardiomyopathy: morphologic findings and interobserver reliabilityDavid A Bluemke, Elizabeth A Krupinski, Theron Ovitt, et al.
Nature Genetics|October 19, 2004
Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathyBrenda Gerull, Arnd Heuser, Thomas Wichter, et al.
Journal of the American College of Cardiology|February 5, 2011
Load-reducing therapy prevents development of arrhythmogenic right ventricular cardiomyopathy in plakoglobin-deficient miceLarissa Fabritz, Mark G Hoogendijk, Brendon P Scicluna, et al.
International Journal of Cardiology|June 21, 2020
Diagnosis of arrhythmogenic cardiomyopathy: The Padua criteriaDomenico Corrado, Martina Perazzolo Marra, Alessandro Zorzi, et al.
International Journal of Cardiology|October 16, 2023
Proposed diagnostic criteria for arrhythmogenic cardiomyopathy: European Task Force consensus reportDomenico Corrado, Aris Anastasakis, Cristina Basso, et al.
European Heart Journal|February 23, 2010
Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force CriteriaFrank I Marcus, William J McKenna, Duane Sherrill, et al.
Circulation|February 23, 2010
Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteriaFrank I Marcus, William J McKenna, Duane Sherrill, et al.
Heart Rhythm|June 30, 2009
Arrhythmogenic right ventricular cardiomyopathy/dysplasia clinical presentation and diagnostic evaluation: results from the North American Multidisciplinary StudyFrank I Marcus, Wojciech Zareba, Hugh Calkins, et al.
Plos Genetics|October 27, 2010
Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathyKlaus Stark, Ulrike B Esslinger, Wibke Reinhard, et al.
Pageof 10

Showing results (81-90 of 92) with videos related to

Sort By:
Pageof 10
Human Molecular Genetics|April 24, 2012
Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathyFelix W Friedrich, Brendan R Wilding, Silke Reischmann, et al.
Cardiology|June 26, 2003
MR Imaging of arrhythmogenic right ventricular cardiomyopathy: morphologic findings and interobserver reliabilityDavid A Bluemke, Elizabeth A Krupinski, Theron Ovitt, et al.
Nature Genetics|October 19, 2004
Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathyBrenda Gerull, Arnd Heuser, Thomas Wichter, et al.
Journal of the American College of Cardiology|February 5, 2011
Load-reducing therapy prevents development of arrhythmogenic right ventricular cardiomyopathy in plakoglobin-deficient miceLarissa Fabritz, Mark G Hoogendijk, Brendon P Scicluna, et al.
International Journal of Cardiology|June 21, 2020
Diagnosis of arrhythmogenic cardiomyopathy: The Padua criteriaDomenico Corrado, Martina Perazzolo Marra, Alessandro Zorzi, et al.
International Journal of Cardiology|October 16, 2023
Proposed diagnostic criteria for arrhythmogenic cardiomyopathy: European Task Force consensus reportDomenico Corrado, Aris Anastasakis, Cristina Basso, et al.
European Heart Journal|February 23, 2010
Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force CriteriaFrank I Marcus, William J McKenna, Duane Sherrill, et al.
Circulation|February 23, 2010
Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteriaFrank I Marcus, William J McKenna, Duane Sherrill, et al.
Heart Rhythm|June 30, 2009
Arrhythmogenic right ventricular cardiomyopathy/dysplasia clinical presentation and diagnostic evaluation: results from the North American Multidisciplinary StudyFrank I Marcus, Wojciech Zareba, Hugh Calkins, et al.
Plos Genetics|October 27, 2010
Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathyKlaus Stark, Ulrike B Esslinger, Wibke Reinhard, et al.
Pageof 10