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Perry Elliott

Showing results (141-150 of 156) with videos related to

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European Heart Journal|October 23, 2019
Arrhythmogenic right ventricular cardiomyopathy: evaluation of the current diagnostic criteria and differential diagnosisDomenico Corrado, Peter J van Tintelen, William J McKenna, et al.
JACC. Heart Failure|July 18, 2025
Genetic and Phenotypic Characterization of Nexilin (NEXN)-Related Cardiomyopathy: Results From a Multicentric StudyMaria Perotto, Alessia Paldino, Francesco Mazzarotto, et al.
Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
The contribution of <i>RBM20</i> truncating variants to human cardiomyopathyBrendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.
Science (New York, N.Y.)|May 25, 2019
Germline selection shapes human mitochondrial DNA diversityWei Wei, Salih Tuna, Michael J Keogh, et al.
European Journal of Heart Failure|May 29, 2021
Prevalence and clinical outcomes of dystrophin-associated dilated cardiomyopathy without severe skeletal myopathyMaria A Restrepo-Cordoba, Karim Wahbi, Anca R Florian, et al.
JAMA Cardiology|April 8, 2026
RBM20 Truncating Variants and Human CardiomyopathyBrendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.
The Journal of Thoracic and Cardiovascular Surgery|April 30, 2021
2020 AHA/ACC guideline for the diagnosis and treatment of patients with hypertrophic cardiomyopathy: A report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines, Steve R Ommen, Seema Mital, et al.
European Heart Journal|August 29, 2014
Atlas of the clinical genetics of human dilated cardiomyopathyJan Haas, Karen S Frese, Barbara Peil, et al.
JAMA Cardiology|February 12, 2025
Arrhythmic Risk Stratification of Carriers of Filamin C Truncating Variants, Marta Gigli, Davide Stolfo, et al.
Heart Rhythm|April 29, 2026
External validation of the DSP-Risk Score for prediction of clinically significant ventricular arrhythmias in primary prevention patients with desmoplakin cardiomyopathy associated genetic variantsAlessio Gasperetti, Barbara Bauce, Alexandros Protonotarios, et al.
Pageof 16

Showing results (141-150 of 156) with videos related to

Sort By:
Pageof 16
European Heart Journal|October 23, 2019
Arrhythmogenic right ventricular cardiomyopathy: evaluation of the current diagnostic criteria and differential diagnosisDomenico Corrado, Peter J van Tintelen, William J McKenna, et al.
JACC. Heart Failure|July 18, 2025
Genetic and Phenotypic Characterization of Nexilin (NEXN)-Related Cardiomyopathy: Results From a Multicentric StudyMaria Perotto, Alessia Paldino, Francesco Mazzarotto, et al.
Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
The contribution of <i>RBM20</i> truncating variants to human cardiomyopathyBrendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.
Science (New York, N.Y.)|May 25, 2019
Germline selection shapes human mitochondrial DNA diversityWei Wei, Salih Tuna, Michael J Keogh, et al.
European Journal of Heart Failure|May 29, 2021
Prevalence and clinical outcomes of dystrophin-associated dilated cardiomyopathy without severe skeletal myopathyMaria A Restrepo-Cordoba, Karim Wahbi, Anca R Florian, et al.
JAMA Cardiology|April 8, 2026
RBM20 Truncating Variants and Human CardiomyopathyBrendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.
The Journal of Thoracic and Cardiovascular Surgery|April 30, 2021
2020 AHA/ACC guideline for the diagnosis and treatment of patients with hypertrophic cardiomyopathy: A report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines, Steve R Ommen, Seema Mital, et al.
European Heart Journal|August 29, 2014
Atlas of the clinical genetics of human dilated cardiomyopathyJan Haas, Karen S Frese, Barbara Peil, et al.
JAMA Cardiology|February 12, 2025
Arrhythmic Risk Stratification of Carriers of Filamin C Truncating Variants, Marta Gigli, Davide Stolfo, et al.
Heart Rhythm|April 29, 2026
External validation of the DSP-Risk Score for prediction of clinically significant ventricular arrhythmias in primary prevention patients with desmoplakin cardiomyopathy associated genetic variantsAlessio Gasperetti, Barbara Bauce, Alexandros Protonotarios, et al.
Pageof 16