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B Sims

Showing results (221-230 of 232) with videos related to

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ESC Heart Failure|April 2, 2026
Effect of Sildenafil on Platelet Activation and Mediators of Vascular Remodeling During LVAD SupportOmar Saeed, Snehal R Patel, Muhammad Farooq, et al.
The Journal of Urology|May 24, 2024
Comparing Magnetic Resonance Imaging and Prostate-Specific Membrane Antigen-Positron Emission Tomography for Prediction of Extraprostatic Extension of Prostate Cancer and Surgical Guidance: A Prospective Nonrandomized Clinical TrialClinton D Bahler, Isamu Tachibana, Mark Tann, et al.
Archives of Environmental Contamination and Toxicology|February 3, 2026
Occurrence and Ecotoxicological Risks of Pharmaceuticals and Illicit Drugs in Effluent and Unsheltered Homelessness-Impacted River SystemsDouglas B Sims, Joshua R Monk, Desta Woldetsadik, et al.
The Annals of Thoracic Surgery|April 14, 2019
Hemolysis and Nonhemorrhagic Stroke During Venoarterial Extracorporeal Membrane OxygenationOmar Saeed, William A Jakobleff, Stephen J Forest, et al.
Journal of Cardiac Failure|October 11, 2021
Full-Time Cardiac Intensive Care Unit Staffing by Heart Failure Specialists and its Association with Mortality RatesDaniel B Sims, Yekaterina Kim, Aleksandr Kalininskiy, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 21, 2014
Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible, and more sensitive for variant detection, than exome sequencingMark B Consugar, Daniel Navarro-Gomez, Emily M Place, et al.
The Annals of Thoracic Surgery|March 12, 2019
Continuous-Flow Left Ventricular Assist Device Survival Improves With Multidisciplinary ApproachUlrich P Jorde, Aman M Shah, Daniel B Sims, et al.
American Journal of Medical Genetics|March 2, 1999
Screen for MAOA mutations in target human groupsD E Schuback, E L Mulligan, K B Sims, et al.
Human Molecular Genetics|January 9, 2013
Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosisKatherine R Smith, Hans-Henrik M Dahl, Laura Canafoglia, et al.
Human Molecular Genetics|November 26, 2013
Human iPSC models of neuronal ceroid lipofuscinosis capture distinct effects of TPP1 and CLN3 mutations on the endocytic pathwayXenia Lojewski, John F Staropoli, Sunita Biswas-Legrand, et al.
Pageof 24

Showing results (221-230 of 232) with videos related to

Sort By:
Pageof 24
ESC Heart Failure|April 2, 2026
Effect of Sildenafil on Platelet Activation and Mediators of Vascular Remodeling During LVAD SupportOmar Saeed, Snehal R Patel, Muhammad Farooq, et al.
The Journal of Urology|May 24, 2024
Comparing Magnetic Resonance Imaging and Prostate-Specific Membrane Antigen-Positron Emission Tomography for Prediction of Extraprostatic Extension of Prostate Cancer and Surgical Guidance: A Prospective Nonrandomized Clinical TrialClinton D Bahler, Isamu Tachibana, Mark Tann, et al.
Archives of Environmental Contamination and Toxicology|February 3, 2026
Occurrence and Ecotoxicological Risks of Pharmaceuticals and Illicit Drugs in Effluent and Unsheltered Homelessness-Impacted River SystemsDouglas B Sims, Joshua R Monk, Desta Woldetsadik, et al.
The Annals of Thoracic Surgery|April 14, 2019
Hemolysis and Nonhemorrhagic Stroke During Venoarterial Extracorporeal Membrane OxygenationOmar Saeed, William A Jakobleff, Stephen J Forest, et al.
Journal of Cardiac Failure|October 11, 2021
Full-Time Cardiac Intensive Care Unit Staffing by Heart Failure Specialists and its Association with Mortality RatesDaniel B Sims, Yekaterina Kim, Aleksandr Kalininskiy, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 21, 2014
Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible, and more sensitive for variant detection, than exome sequencingMark B Consugar, Daniel Navarro-Gomez, Emily M Place, et al.
The Annals of Thoracic Surgery|March 12, 2019
Continuous-Flow Left Ventricular Assist Device Survival Improves With Multidisciplinary ApproachUlrich P Jorde, Aman M Shah, Daniel B Sims, et al.
American Journal of Medical Genetics|March 2, 1999
Screen for MAOA mutations in target human groupsD E Schuback, E L Mulligan, K B Sims, et al.
Human Molecular Genetics|January 9, 2013
Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosisKatherine R Smith, Hans-Henrik M Dahl, Laura Canafoglia, et al.
Human Molecular Genetics|November 26, 2013
Human iPSC models of neuronal ceroid lipofuscinosis capture distinct effects of TPP1 and CLN3 mutations on the endocytic pathwayXenia Lojewski, John F Staropoli, Sunita Biswas-Legrand, et al.
Pageof 24