Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

P Judge

Showing results (271-280 of 354) with videos related to

Pageof 36
Sort By:
The New England Journal of Medicine|April 13, 2022
Mitapivat versus Placebo for Pyruvate Kinase DeficiencyHanny Al-Samkari, Frédéric Galactéros, Andreas Glenthøj, et al.
Cell Reports|January 12, 2017
Neonatal Transplantation Confers Maturation of PSC-Derived Cardiomyocytes Conducive to Modeling CardiomyopathyGun-Sik Cho, Dong I Lee, Emmanouil Tampakakis, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|April 5, 2016
Right ventricular afterload sensitivity dramatically increases after left ventricular assist device implantation: A multi-center hemodynamic analysisBrian A Houston, Rohan J Kalathiya, Steven Hsu, et al.
Journal of Medical Genetics|March 31, 2006
The molecular genetics of Marfan syndrome and related disordersP N Robinson, E Arteaga-Solis, C Baldock, et al.
Journal of Cardiac Failure|April 3, 2012
Genetic testing for dilated cardiomyopathy in clinical practiceNeal K Lakdawala, Birgit H Funke, Samantha Baxter, et al.
JCI Insight|August 4, 2017
Nonmyocyte ERK1/2 signaling contributes to load-induced cardiomyopathy in Marfan miceRosanne Rouf, Elena Gallo MacFarlane, Eiki Takimoto, et al.
Science Translational Medicine|April 9, 2010
Mutations in fibrillin-1 cause congenital scleroderma: stiff skin syndromeB L Loeys, E E Gerber, D Riegert-Johnson, et al.
JACC. Clinical Electrophysiology|May 16, 2018
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy in the Pediatric Population: Clinical Characterization and Comparison With Adult-Onset DiseaseAnneline S J M Te Riele, Cynthia A James, Abhishek C Sawant, et al.
Journal of Cardiovascular Electrophysiology|May 1, 2018
Identification of sarcomeric variants in probands with a clinical diagnosis of arrhythmogenic right ventricular cardiomyopathy (ARVC)Brittney Murray, Edgar T Hoorntje, Anneline S J M Te Riele, et al.
Circulation. Genomic and Precision Medicine|April 8, 2021
International Evidence Based Reappraisal of Genes Associated With Arrhythmogenic Right Ventricular Cardiomyopathy Using the Clinical Genome Resource FrameworkCynthia A James, Jan D H Jongbloed, Ray E Hershberger, et al.
Pageof 36

Showing results (271-280 of 354) with videos related to

Sort By:
Pageof 36
The New England Journal of Medicine|April 13, 2022
Mitapivat versus Placebo for Pyruvate Kinase DeficiencyHanny Al-Samkari, Frédéric Galactéros, Andreas Glenthøj, et al.
Cell Reports|January 12, 2017
Neonatal Transplantation Confers Maturation of PSC-Derived Cardiomyocytes Conducive to Modeling CardiomyopathyGun-Sik Cho, Dong I Lee, Emmanouil Tampakakis, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|April 5, 2016
Right ventricular afterload sensitivity dramatically increases after left ventricular assist device implantation: A multi-center hemodynamic analysisBrian A Houston, Rohan J Kalathiya, Steven Hsu, et al.
Journal of Medical Genetics|March 31, 2006
The molecular genetics of Marfan syndrome and related disordersP N Robinson, E Arteaga-Solis, C Baldock, et al.
Journal of Cardiac Failure|April 3, 2012
Genetic testing for dilated cardiomyopathy in clinical practiceNeal K Lakdawala, Birgit H Funke, Samantha Baxter, et al.
JCI Insight|August 4, 2017
Nonmyocyte ERK1/2 signaling contributes to load-induced cardiomyopathy in Marfan miceRosanne Rouf, Elena Gallo MacFarlane, Eiki Takimoto, et al.
Science Translational Medicine|April 9, 2010
Mutations in fibrillin-1 cause congenital scleroderma: stiff skin syndromeB L Loeys, E E Gerber, D Riegert-Johnson, et al.
JACC. Clinical Electrophysiology|May 16, 2018
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy in the Pediatric Population: Clinical Characterization and Comparison With Adult-Onset DiseaseAnneline S J M Te Riele, Cynthia A James, Abhishek C Sawant, et al.
Journal of Cardiovascular Electrophysiology|May 1, 2018
Identification of sarcomeric variants in probands with a clinical diagnosis of arrhythmogenic right ventricular cardiomyopathy (ARVC)Brittney Murray, Edgar T Hoorntje, Anneline S J M Te Riele, et al.
Circulation. Genomic and Precision Medicine|April 8, 2021
International Evidence Based Reappraisal of Genes Associated With Arrhythmogenic Right Ventricular Cardiomyopathy Using the Clinical Genome Resource FrameworkCynthia A James, Jan D H Jongbloed, Ray E Hershberger, et al.
Pageof 36