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David Wendler

Showing results (191-200 of 214) with videos related to

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Archives of Internal Medicine|March 30, 2005
Research with stored biological samples: what do research participants want?Donna T Chen, Donald L Rosenstein, Palaniappan Muthappan, et al.
Clinical Trials (London, England)|October 4, 2018
Understanding preferences regarding consent for pragmatic trials in acute careNeal W Dickert, David Wendler, Chandan M Devireddy, et al.
JAMA Oncology|March 10, 2017
Patients' and Parents' Needs, Attitudes, and Perceptions About Early Palliative Care Integration in Pediatric OncologyDeena R Levine, Belinda N Mandrell, April Sykes, et al.
Journal of the American College of Cardiology|March 3, 2018
Consent for Pragmatic Trials in Acute Myocardial InfarctionNeal W Dickert, David Wendler, Chandan M Devireddy, et al.
Prenatal Diagnosis|December 9, 2023
Precarious hope: Ethical considerations for offering experimental fetal therapies outside of research after initial studies in humansSaskia Hendriks, Janyne Althaus, Meredith A Atkinson, et al.
American Journal of Public Health|June 4, 2005
Quality of parental consent in a Ugandan malaria studyChristine Pace, Ambrose Talisuna, David Wendler, et al.
Clinical Trials (London, England)|November 26, 2024
Ethical considerations for sharing aggregate results from pragmatic clinical trialsStephanie R Morain, Abigail Brickler, Joseph Ali, et al.
Plos Medicine|December 2, 2005
Are racial and ethnic minorities less willing to participate in health research?David Wendler, Raynard Kington, Jennifer Madans, et al.
Contemporary Clinical Trials|February 17, 2022
Ethical and epistemic issues in the design and conduct of pragmatic stepped-wedge cluster randomized clinical trialsCarole A Federico, Patrick J Heagerty, John Lantos, et al.
Journal of Empirical Research on Human Research Ethics : JERHRE|February 3, 2018
Broad Consent for Research on Biospecimens: The Views of Actual Donors at Four U.S. Medical CentersTeddy D Warner, Carol J Weil, Christopher Andry, et al.
Pageof 22

Showing results (191-200 of 214) with videos related to

Sort By:
Pageof 22
Archives of Internal Medicine|March 30, 2005
Research with stored biological samples: what do research participants want?Donna T Chen, Donald L Rosenstein, Palaniappan Muthappan, et al.
Clinical Trials (London, England)|October 4, 2018
Understanding preferences regarding consent for pragmatic trials in acute careNeal W Dickert, David Wendler, Chandan M Devireddy, et al.
JAMA Oncology|March 10, 2017
Patients' and Parents' Needs, Attitudes, and Perceptions About Early Palliative Care Integration in Pediatric OncologyDeena R Levine, Belinda N Mandrell, April Sykes, et al.
Journal of the American College of Cardiology|March 3, 2018
Consent for Pragmatic Trials in Acute Myocardial InfarctionNeal W Dickert, David Wendler, Chandan M Devireddy, et al.
Prenatal Diagnosis|December 9, 2023
Precarious hope: Ethical considerations for offering experimental fetal therapies outside of research after initial studies in humansSaskia Hendriks, Janyne Althaus, Meredith A Atkinson, et al.
American Journal of Public Health|June 4, 2005
Quality of parental consent in a Ugandan malaria studyChristine Pace, Ambrose Talisuna, David Wendler, et al.
Clinical Trials (London, England)|November 26, 2024
Ethical considerations for sharing aggregate results from pragmatic clinical trialsStephanie R Morain, Abigail Brickler, Joseph Ali, et al.
Plos Medicine|December 2, 2005
Are racial and ethnic minorities less willing to participate in health research?David Wendler, Raynard Kington, Jennifer Madans, et al.
Contemporary Clinical Trials|February 17, 2022
Ethical and epistemic issues in the design and conduct of pragmatic stepped-wedge cluster randomized clinical trialsCarole A Federico, Patrick J Heagerty, John Lantos, et al.
Journal of Empirical Research on Human Research Ethics : JERHRE|February 3, 2018
Broad Consent for Research on Biospecimens: The Views of Actual Donors at Four U.S. Medical CentersTeddy D Warner, Carol J Weil, Christopher Andry, et al.
Pageof 22