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J Ackerman

Showing results (501-510 of 1,428) with videos related to

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Heart Rhythm|February 11, 2012
Potential depot medroxyprogesterone acetate-triggered torsades de pointes in a case of congenital type 2 long QT syndromeJohn R Giudicessi, Brian C Brost, Kyle D Traynor, et al.
Nanotechnology|August 6, 2011
Enzyme specific activity in functionalized nanoporous supportsChenghong Lei, Thereza A Soares, Yongsoon Shin, et al.
Heart Rhythm|October 18, 2011
Congenital type 1 long QT syndrome unmasked by a highly caffeinated energy drinkKeith A Dufendach, Justin M Horner, Bryan C Cannon, et al.
ACS Nano|November 17, 2015
Plasmon-Exciton Interactions Probed Using Spatial Coentrapment of Nanoparticles by Topological SingularitiesPaul J Ackerman, Haridas Mundoor, Ivan I Smalyukh, et al.
Journal of the American College of Cardiology|November 7, 2015
Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 10: The Cardiac Channelopathies: A Scientific Statement From the American Heart Association and American College of CardiologyMichael J Ackerman, Douglas P Zipes, Richard J Kovacs, et al.
Circulation. Genomic and Precision Medicine|November 16, 2020
Patients With Hypertrophic Cardiomyopathy Deemed Genotype Negative Based on Research Grade Genetic Analysis: Time for Repeat Diagnostic Testing With Next-Generation SequencingBailey J O'Hare, J Martijn Bos, David J Tester, et al.
Circulation|February 21, 2020
Variant Frequency and Clinical Phenotype Call Into Question the Nature of Minor, Nonsyndromic Long-QT Syndrome-Susceptibility Gene-Disease AssociationsJohn R Giudicessi, Ram K Rohatgi, David J Tester, et al.
Circulation|September 24, 2020
Urgent Need for Studies of the Late Effects of SARS-CoV-2 on the Cardiovascular SystemJoseph J Maleszewski, Phillip M Young, Michael J Ackerman, et al.
The Journal of Hand Surgery|November 6, 2022
Classic Timothy Syndrome Associated With Bilateral Border Digit Syndactyly: A Case SeriesEugene E Zheng, Francisco R Avila, Michael J Ackerman, et al.
Heart Rhythm|September 2, 2018
A pore-localizing CACNA1C-E1115K missense mutation, identified in a patient with idiopathic QT prolongation, bradycardia, and autism spectrum disorder, converts the L-type calcium channel into a hybrid nonselective monovalent cation channelDan Ye, David J Tester, Wei Zhou, et al.
Pageof 143

Showing results (501-510 of 1,428) with videos related to

Sort By:
Pageof 143
Heart Rhythm|February 11, 2012
Potential depot medroxyprogesterone acetate-triggered torsades de pointes in a case of congenital type 2 long QT syndromeJohn R Giudicessi, Brian C Brost, Kyle D Traynor, et al.
Nanotechnology|August 6, 2011
Enzyme specific activity in functionalized nanoporous supportsChenghong Lei, Thereza A Soares, Yongsoon Shin, et al.
Heart Rhythm|October 18, 2011
Congenital type 1 long QT syndrome unmasked by a highly caffeinated energy drinkKeith A Dufendach, Justin M Horner, Bryan C Cannon, et al.
ACS Nano|November 17, 2015
Plasmon-Exciton Interactions Probed Using Spatial Coentrapment of Nanoparticles by Topological SingularitiesPaul J Ackerman, Haridas Mundoor, Ivan I Smalyukh, et al.
Journal of the American College of Cardiology|November 7, 2015
Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 10: The Cardiac Channelopathies: A Scientific Statement From the American Heart Association and American College of CardiologyMichael J Ackerman, Douglas P Zipes, Richard J Kovacs, et al.
Circulation. Genomic and Precision Medicine|November 16, 2020
Patients With Hypertrophic Cardiomyopathy Deemed Genotype Negative Based on Research Grade Genetic Analysis: Time for Repeat Diagnostic Testing With Next-Generation SequencingBailey J O'Hare, J Martijn Bos, David J Tester, et al.
Circulation|February 21, 2020
Variant Frequency and Clinical Phenotype Call Into Question the Nature of Minor, Nonsyndromic Long-QT Syndrome-Susceptibility Gene-Disease AssociationsJohn R Giudicessi, Ram K Rohatgi, David J Tester, et al.
Circulation|September 24, 2020
Urgent Need for Studies of the Late Effects of SARS-CoV-2 on the Cardiovascular SystemJoseph J Maleszewski, Phillip M Young, Michael J Ackerman, et al.
The Journal of Hand Surgery|November 6, 2022
Classic Timothy Syndrome Associated With Bilateral Border Digit Syndactyly: A Case SeriesEugene E Zheng, Francisco R Avila, Michael J Ackerman, et al.
Heart Rhythm|September 2, 2018
A pore-localizing CACNA1C-E1115K missense mutation, identified in a patient with idiopathic QT prolongation, bradycardia, and autism spectrum disorder, converts the L-type calcium channel into a hybrid nonselective monovalent cation channelDan Ye, David J Tester, Wei Zhou, et al.
Pageof 143