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Showing results (151-160 of 353) with videos related to

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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.
British Journal of Pharmacology|March 7, 2007
Endothelial dysfunction and compromised eNOS/Akt signaling in the thoracic aorta during the progression of Marfan syndromeA W Y Chung, K Au Yeung, S F Cortes, 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.
Oncology Nursing Forum|December 16, 2021
A Descriptive Survey Study of Patient Needs and Preferences for Cancer Pain Self-Management SupportAlice Jane Anderson, Angela Starkweather, Xiaomei Cong, et al.
Pageof 36

Showing results (151-160 of 353) with videos related to

Sort By:
Pageof 36
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.
British Journal of Pharmacology|March 7, 2007
Endothelial dysfunction and compromised eNOS/Akt signaling in the thoracic aorta during the progression of Marfan syndromeA W Y Chung, K Au Yeung, S F Cortes, 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.
Oncology Nursing Forum|December 16, 2021
A Descriptive Survey Study of Patient Needs and Preferences for Cancer Pain Self-Management SupportAlice Jane Anderson, Angela Starkweather, Xiaomei Cong, et al.
Pageof 36