Search research articles
Contact Us
Filters
Showing results (221-230 of 232) with videos related to
Page
of 24
Sort By:
ESC Heart Failure
|
April 2, 2026
Effect of Sildenafil on Platelet Activation and Mediators of Vascular Remodeling During LVAD Support
Omar 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 Trial
Clinton 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 Systems
Douglas 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 Oxygenation
Omar 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 Rates
Daniel 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 sequencing
Mark 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 Approach
Ulrich 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 groups
D 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 lipofuscinosis
Katherine 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 pathway
Xenia Lojewski, John F Staropoli, Sunita Biswas-Legrand, et al.
Page
of 24
Search research articles
Search
Showing results (221-230 of 232) with videos related to
Sort By:
Page
of 24
ESC Heart Failure
|
April 2, 2026
Effect of Sildenafil on Platelet Activation and Mediators of Vascular Remodeling During LVAD Support
Omar 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 Trial
Clinton 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 Systems
Douglas 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 Oxygenation
Omar 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 Rates
Daniel 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 sequencing
Mark 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 Approach
Ulrich 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 groups
D 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 lipofuscinosis
Katherine 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 pathway
Xenia Lojewski, John F Staropoli, Sunita Biswas-Legrand, et al.
Page
of 24