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J Ackerman

Showing results (931-940 of 1,140) with videos related to

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European Heart Journal. Cardiovascular Imaging|February 29, 2016
Pulmonary hypertension is associated with worse survival in hypertrophic cardiomyopathyKevin C Ong, Jeffrey B Geske, Virginia B Hebl, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 21, 2021
De novo mutations in childhood cases of sudden unexplained death that disrupt intracellular Ca<sup>2+</sup> regulationMatthew Halvorsen, Laura Gould, Xiaohan Wang, et al.
Nature Medicine|January 3, 2001
Impaired prostate tumorigenesis in Egr1-deficient miceS A Abdulkadir, Z Qu, E Garabedian, et al.
Circulation. Genomic and Precision Medicine|October 26, 2018
Effect of Ascertainment Bias on Estimates of Patient Mortality in Inherited Cardiac DiseasesEline A Nannenberg, Ingrid A W van Rijsingen, Paul A van der Zwaag, et al.
Echocardiography (Mount Kisco, N.Y.)|December 16, 2020
Conversion of left atrial volume to diameter for automated estimation of sudden cardiac death risk in hypertrophic cardiomyopathyHuzefa Bhopalwala, Nakeya Dewaswala, Sijia Liu, et al.
Circulation|February 23, 2011
Disrupted junctional membrane complexes and hyperactive ryanodine receptors after acute junctophilin knockdown in miceRalph J van Oort, Alejandro Garbino, Wei Wang, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|October 7, 2016
Outcomes of lead extraction without subsequent device reimplantationMohammed A Al-Hijji, Ammar M Killu, Omid Yousefian, et al.
Circulation|May 25, 2005
Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotypeLi Zhang, D Woodrow Benson, Martin Tristani-Firouzi, et al.
Circulation Research|October 22, 2016
A Precision Medicine Approach to the Rescue of Function on Malignant Calmodulinopathic Long-QT SyndromeWorawan B Limpitikul, Ivy E Dick, David J Tester, et al.
Circulation. Cardiovascular Genetics|August 12, 2011
Risk of syncope in family members who are genotype-negative for a family-associated long-QT syndrome mutationAlon Barsheshet, Arthur J Moss, Scott McNitt, et al.
Pageof 114

Showing results (931-940 of 1,140) with videos related to

Sort By:
Pageof 114
European Heart Journal. Cardiovascular Imaging|February 29, 2016
Pulmonary hypertension is associated with worse survival in hypertrophic cardiomyopathyKevin C Ong, Jeffrey B Geske, Virginia B Hebl, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 21, 2021
De novo mutations in childhood cases of sudden unexplained death that disrupt intracellular Ca<sup>2+</sup> regulationMatthew Halvorsen, Laura Gould, Xiaohan Wang, et al.
Nature Medicine|January 3, 2001
Impaired prostate tumorigenesis in Egr1-deficient miceS A Abdulkadir, Z Qu, E Garabedian, et al.
Circulation. Genomic and Precision Medicine|October 26, 2018
Effect of Ascertainment Bias on Estimates of Patient Mortality in Inherited Cardiac DiseasesEline A Nannenberg, Ingrid A W van Rijsingen, Paul A van der Zwaag, et al.
Echocardiography (Mount Kisco, N.Y.)|December 16, 2020
Conversion of left atrial volume to diameter for automated estimation of sudden cardiac death risk in hypertrophic cardiomyopathyHuzefa Bhopalwala, Nakeya Dewaswala, Sijia Liu, et al.
Circulation|February 23, 2011
Disrupted junctional membrane complexes and hyperactive ryanodine receptors after acute junctophilin knockdown in miceRalph J van Oort, Alejandro Garbino, Wei Wang, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|October 7, 2016
Outcomes of lead extraction without subsequent device reimplantationMohammed A Al-Hijji, Ammar M Killu, Omid Yousefian, et al.
Circulation|May 25, 2005
Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotypeLi Zhang, D Woodrow Benson, Martin Tristani-Firouzi, et al.
Circulation Research|October 22, 2016
A Precision Medicine Approach to the Rescue of Function on Malignant Calmodulinopathic Long-QT SyndromeWorawan B Limpitikul, Ivy E Dick, David J Tester, et al.
Circulation. Cardiovascular Genetics|August 12, 2011
Risk of syncope in family members who are genotype-negative for a family-associated long-QT syndrome mutationAlon Barsheshet, Arthur J Moss, Scott McNitt, et al.
Pageof 114