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 (61-70 of 260) with videos related to

Pageof 26
Sort By:
Molecular Genetics & Genomic Medicine|April 28, 2018
Protein molecular modeling techniques investigating novel TAB2 variant R347X causing cardiomyopathy and congenital heart defects in multigenerational familyThomas R Caulfield, John E Richter, Emily E Brown, et al.
Circulation. Genomic and Precision Medicine|September 17, 2020
Influence of Panel Selection on Yield of Clinically Useful Variants in Arrhythmogenic Right Ventricular Cardiomyopathy FamiliesBrittney Murray, Crystal Tichnell, Harikrishna Tandri, et al.
Future Cardiology|March 17, 2022
How did transthyretin amyloid cardiomyopathy progress in patients who took placebo in the study ATTR-ACT? A plain language summaryJose Nativi-Nicolau, Daniel P Judge, James E Hoffman, et al.
Human Molecular Genetics|August 14, 2003
Allelic variation in normal human FBN1 expression in a family with Marfan syndrome: a potential modifier of phenotype?Sarah Hutchinson, Andre Furger, Dorothy Halliday, et al.
Journal of Cardiovascular Electrophysiology|December 1, 2010
Reader- and instrument-dependent variability in the electrocardiographic assessment of arrhythmogenic right ventricular dysplasia/cardiomyopathyRahul Jain, Harikrishna Tandri, Amy Daly, et al.
Future Cardiology|April 3, 2023
Long-term effectiveness of ARRY-371797 in people with dilated cardiomyopathy and a faulty LMNA gene: a plain language summaryDaniel P Judge, Matthew Rg Taylor, Huihua Li, et al.
Circulation. Genomic and Precision Medicine|July 21, 2022
<i>PLEKHM2</i> Loss-of-Function Is Associated With Dilated CardiomyopathyJessica Atkins, Cortney Gensemer, Kimberly Foil, et al.
Circulation Research|July 21, 2007
Loss of elastic fiber integrity and reduction of vascular smooth muscle contraction resulting from the upregulated activities of matrix metalloproteinase-2 and -9 in the thoracic aortic aneurysm in Marfan syndromeAda W Y Chung, Karen Au Yeung, George G S Sandor, et al.
Heartrhythm Case Reports|September 26, 2015
Surgical Correction of Tricuspid Regurgitation in Patients with ARVD/CGeorge Katritsis, Ashish S Shah, Cynthia A James, et al.
Circulation. Genomic and Precision Medicine|November 16, 2020
Genetic Dilated Cardiomyopathy Due to TTN Variants Without Known Familial DiseaseEmily E Brown, Brittney Murray, Joban Vaishnav, et al.
Pageof 26

Showing results (61-70 of 260) with videos related to

Sort By:
Pageof 26
Molecular Genetics & Genomic Medicine|April 28, 2018
Protein molecular modeling techniques investigating novel TAB2 variant R347X causing cardiomyopathy and congenital heart defects in multigenerational familyThomas R Caulfield, John E Richter, Emily E Brown, et al.
Circulation. Genomic and Precision Medicine|September 17, 2020
Influence of Panel Selection on Yield of Clinically Useful Variants in Arrhythmogenic Right Ventricular Cardiomyopathy FamiliesBrittney Murray, Crystal Tichnell, Harikrishna Tandri, et al.
Future Cardiology|March 17, 2022
How did transthyretin amyloid cardiomyopathy progress in patients who took placebo in the study ATTR-ACT? A plain language summaryJose Nativi-Nicolau, Daniel P Judge, James E Hoffman, et al.
Human Molecular Genetics|August 14, 2003
Allelic variation in normal human FBN1 expression in a family with Marfan syndrome: a potential modifier of phenotype?Sarah Hutchinson, Andre Furger, Dorothy Halliday, et al.
Journal of Cardiovascular Electrophysiology|December 1, 2010
Reader- and instrument-dependent variability in the electrocardiographic assessment of arrhythmogenic right ventricular dysplasia/cardiomyopathyRahul Jain, Harikrishna Tandri, Amy Daly, et al.
Future Cardiology|April 3, 2023
Long-term effectiveness of ARRY-371797 in people with dilated cardiomyopathy and a faulty LMNA gene: a plain language summaryDaniel P Judge, Matthew Rg Taylor, Huihua Li, et al.
Circulation. Genomic and Precision Medicine|July 21, 2022
<i>PLEKHM2</i> Loss-of-Function Is Associated With Dilated CardiomyopathyJessica Atkins, Cortney Gensemer, Kimberly Foil, et al.
Circulation Research|July 21, 2007
Loss of elastic fiber integrity and reduction of vascular smooth muscle contraction resulting from the upregulated activities of matrix metalloproteinase-2 and -9 in the thoracic aortic aneurysm in Marfan syndromeAda W Y Chung, Karen Au Yeung, George G S Sandor, et al.
Heartrhythm Case Reports|September 26, 2015
Surgical Correction of Tricuspid Regurgitation in Patients with ARVD/CGeorge Katritsis, Ashish S Shah, Cynthia A James, et al.
Circulation. Genomic and Precision Medicine|November 16, 2020
Genetic Dilated Cardiomyopathy Due to TTN Variants Without Known Familial DiseaseEmily E Brown, Brittney Murray, Joban Vaishnav, et al.
Pageof 26