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

Daniel P Judge

Showing results (81-90 of 260) with videos related to

Pageof 26
Sort By:
Journal of Cardiac Failure|January 16, 2016
Lack of Relationship Between Serum Cardiac Troponin I Level and Giant Cell Myocarditis Diagnosis and OutcomesNisha A Gilotra, Nicole Minkove, Mosi K Bennett, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|February 22, 2012
The diagnosis of hypertrophic cardiomyopathy by cardiovascular magnetic resonanceRadwa A Noureldin, Songtao Liu, Marcelo S Nacif, et al.
Journal of Clinical and Translational Science|February 6, 2025
Using technology to increase reach and optimize consent experience for a large-scale research programEmma Coen, Daniel P Judge, Samantha Norman, et al.
American Journal of Human Genetics|April 2, 2003
KLOTHO allele status and the risk of early-onset occult coronary artery diseaseDan E Arking, Diane M Becker, Lisa R Yanek, et al.
Circulation. Heart Failure|April 16, 2015
Tafamidis in transthyretin amyloid cardiomyopathy: effects on transthyretin stabilization and clinical outcomesMathew S Maurer, Donna R Grogan, Daniel P Judge, et al.
International Journal of Molecular Sciences|November 26, 2022
Efficacy and Safety of Angiotensin Receptor Blockers in a Pre-Clinical Model of Arrhythmogenic CardiomyopathyMaicon Landim-Vieira, Aida Rahimi Kahmini, Morgan Engel, et al.
HGG Advances|March 21, 2024
A power-based sliding window approach to evaluate the clinical impact of rare genetic variants in the nucleotide sequence or the spatial position of the folded proteinElizabeth T Cirulli, Kelly M Schiabor Barrett, Alexandre Bolze, et al.
Human Molecular Genetics|October 21, 2020
The prevalent I686T human variant and loss-of-function mutations in the cardiomyocyte-specific kinase gene TNNI3K cause adverse contractility and concentric remodeling in micePeiheng Gan, Catalin Baicu, Hirofumi Watanabe, et al.
Cardiology in the Young|June 15, 2019
Genetic aetiologies should be considered in paediatric cases of acute heart failure presumed to be myocarditisEmily E Brown, Kristen Nelson McMilllan, Marc K Halushka, et al.
American Journal of Medical Genetics. Part A|January 12, 2013
A family with a complex clinical presentation characterized by arrhythmogenic right ventricular dysplasia/cardiomyopathy and features of branchio-oculo-facial syndromeBrittney Murray, Rohan Wagle, Nuria Amat-Alarcon, et al.
Pageof 26

Showing results (81-90 of 260) with videos related to

Sort By:
Pageof 26
Journal of Cardiac Failure|January 16, 2016
Lack of Relationship Between Serum Cardiac Troponin I Level and Giant Cell Myocarditis Diagnosis and OutcomesNisha A Gilotra, Nicole Minkove, Mosi K Bennett, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|February 22, 2012
The diagnosis of hypertrophic cardiomyopathy by cardiovascular magnetic resonanceRadwa A Noureldin, Songtao Liu, Marcelo S Nacif, et al.
Journal of Clinical and Translational Science|February 6, 2025
Using technology to increase reach and optimize consent experience for a large-scale research programEmma Coen, Daniel P Judge, Samantha Norman, et al.
American Journal of Human Genetics|April 2, 2003
KLOTHO allele status and the risk of early-onset occult coronary artery diseaseDan E Arking, Diane M Becker, Lisa R Yanek, et al.
Circulation. Heart Failure|April 16, 2015
Tafamidis in transthyretin amyloid cardiomyopathy: effects on transthyretin stabilization and clinical outcomesMathew S Maurer, Donna R Grogan, Daniel P Judge, et al.
International Journal of Molecular Sciences|November 26, 2022
Efficacy and Safety of Angiotensin Receptor Blockers in a Pre-Clinical Model of Arrhythmogenic CardiomyopathyMaicon Landim-Vieira, Aida Rahimi Kahmini, Morgan Engel, et al.
HGG Advances|March 21, 2024
A power-based sliding window approach to evaluate the clinical impact of rare genetic variants in the nucleotide sequence or the spatial position of the folded proteinElizabeth T Cirulli, Kelly M Schiabor Barrett, Alexandre Bolze, et al.
Human Molecular Genetics|October 21, 2020
The prevalent I686T human variant and loss-of-function mutations in the cardiomyocyte-specific kinase gene TNNI3K cause adverse contractility and concentric remodeling in micePeiheng Gan, Catalin Baicu, Hirofumi Watanabe, et al.
Cardiology in the Young|June 15, 2019
Genetic aetiologies should be considered in paediatric cases of acute heart failure presumed to be myocarditisEmily E Brown, Kristen Nelson McMilllan, Marc K Halushka, et al.
American Journal of Medical Genetics. Part A|January 12, 2013
A family with a complex clinical presentation characterized by arrhythmogenic right ventricular dysplasia/cardiomyopathy and features of branchio-oculo-facial syndromeBrittney Murray, Rohan Wagle, Nuria Amat-Alarcon, et al.
Pageof 26