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Melanie Care

Showing results (1-10 of 39) with videos related to

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Current Cardiology Reports|August 17, 2017
Genetic Testing in Inherited Heart Diseases: Practical Considerations for CliniciansMelanie Care, Vijay Chauhan, Danna Spears
Forensic Sciences Research|September 7, 2019
Evaluation of cardiac hypertrophy in the setting of sudden cardiac deathKristopher S Cunningham, Danna A Spears, Melanie Care
The American Journal of Cardiology|July 14, 2022
Secondary Findings Using Broad Pan Cardiomyopathy and Arrhythmia Panels in Patients With a Personal or Family History of Inherited Cardiomyopathy or Arrhythmia SyndromeEmily Smith, Melanie Care, Carolyn Burke-Martindale, et al.
Heart Rhythm|August 18, 2020
Primary prevention implantable cardioverter-defibrillators in hypertrophic cardiomyopathy-Are there predictors of appropriate therapy?Adaya Weissler-Snir, Paul Dorian, Harry Rakowski, et al.
Pacing and Clinical Electrophysiology : PACE|February 4, 2017
Evaluation of Prolonged QT Interval: Structural Heart Disease Mimicking Long QT SyndromeAdaya Weissler-Snir, Michael H Gollob, Vijay Chauhan, et al.
Circulation. Cardiovascular Genetics|April 23, 2011
Sarcomere protein gene mutations in patients with apical hypertrophic cardiomyopathyChristiane Gruner, Melanie Care, Katherine Siminovitch, et al.
Journal of the American Heart Association|November 28, 2023
Assessment of Severity of Long QT Syndrome Phenotype and Risk of Fetal DeathLisa Albertini, Jordan Ezekian, Melanie Care, et al.
Cancers|November 16, 2018
Next-Generation Service Delivery: A Scoping Review of Patient Outcomes Associated with Alternative Models of Genetic Counseling and Genetic Testing for Hereditary CancerJeanna M McCuaig, Susan Randall Armel, Melanie Care, et al.
American Journal of Medical Genetics. Part A|February 18, 2017
Whole exome sequencing identified 1 base pair novel deletion in BCL2-associated athanogene 3 (BAG3) gene associated with severe dilated cardiomyopathy (DCM) requiring heart transplant in multiple family membersMuhammad Arshad Rafiq, Ayeshah Chaudhry, Melanie Care, et al.
Radiology. Cardiothoracic Imaging|January 2, 2024
Cardiac MRI and Clinical Outcomes in <i>TMEM43</i> Arrhythmogenic CardiomyopathyJoão Matos, Emmi Helle, Melanie Care, et al.
Pageof 4

Showing results (1-10 of 39) with videos related to

Sort By:
Pageof 4
Current Cardiology Reports|August 17, 2017
Genetic Testing in Inherited Heart Diseases: Practical Considerations for CliniciansMelanie Care, Vijay Chauhan, Danna Spears
Forensic Sciences Research|September 7, 2019
Evaluation of cardiac hypertrophy in the setting of sudden cardiac deathKristopher S Cunningham, Danna A Spears, Melanie Care
The American Journal of Cardiology|July 14, 2022
Secondary Findings Using Broad Pan Cardiomyopathy and Arrhythmia Panels in Patients With a Personal or Family History of Inherited Cardiomyopathy or Arrhythmia SyndromeEmily Smith, Melanie Care, Carolyn Burke-Martindale, et al.
Heart Rhythm|August 18, 2020
Primary prevention implantable cardioverter-defibrillators in hypertrophic cardiomyopathy-Are there predictors of appropriate therapy?Adaya Weissler-Snir, Paul Dorian, Harry Rakowski, et al.
Pacing and Clinical Electrophysiology : PACE|February 4, 2017
Evaluation of Prolonged QT Interval: Structural Heart Disease Mimicking Long QT SyndromeAdaya Weissler-Snir, Michael H Gollob, Vijay Chauhan, et al.
Circulation. Cardiovascular Genetics|April 23, 2011
Sarcomere protein gene mutations in patients with apical hypertrophic cardiomyopathyChristiane Gruner, Melanie Care, Katherine Siminovitch, et al.
Journal of the American Heart Association|November 28, 2023
Assessment of Severity of Long QT Syndrome Phenotype and Risk of Fetal DeathLisa Albertini, Jordan Ezekian, Melanie Care, et al.
Cancers|November 16, 2018
Next-Generation Service Delivery: A Scoping Review of Patient Outcomes Associated with Alternative Models of Genetic Counseling and Genetic Testing for Hereditary CancerJeanna M McCuaig, Susan Randall Armel, Melanie Care, et al.
American Journal of Medical Genetics. Part A|February 18, 2017
Whole exome sequencing identified 1 base pair novel deletion in BCL2-associated athanogene 3 (BAG3) gene associated with severe dilated cardiomyopathy (DCM) requiring heart transplant in multiple family membersMuhammad Arshad Rafiq, Ayeshah Chaudhry, Melanie Care, et al.
Radiology. Cardiothoracic Imaging|January 2, 2024
Cardiac MRI and Clinical Outcomes in <i>TMEM43</i> Arrhythmogenic CardiomyopathyJoão Matos, Emmi Helle, Melanie Care, et al.
Pageof 4