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The New England Journal of Medicine|December 27, 2002
Descriptions of benefits and risks in consent forms for phase 1 oncology trialsSam Horng, Ezekiel J Emanuel, Benjamin Wilfond, et al.BMC Medical Ethics|July 29, 2023
Communication of patients' and family members' ethical concerns to their healthcare providersMariam Noorulhuda, Christine Grady, Paul Wakim, et al.Journal of Women'S Health (2002)|August 9, 2011
Clinical research enrolling pregnant women: a workshop summaryMary A Foulkes, Christine Grady, Catherine Y Spong, et al.The American Journal of Bioethics : AJOB|May 23, 2020
Patient and Family Descriptions of Ethical ConcernsHae Lin Cho, Christine Grady, Anita Tarzian, et al.The American Journal of Bioethics : AJOB|May 3, 2011
Dealing with the long-term social implications of researchAlan Fleischman, Carol Levine, Lisa Eckenwiler, et al.Palliative & Supportive Care|October 3, 2014
Patients' priorities for treatment decision making during periods of incapacity: quantitative surveyAnnette Rid, Robert Wesley, Mark Pavlick, et al.Annals of Internal Medicine|July 29, 2015
Pragmatic Randomized Trials Without Standard Informed Consent?: A National SurveyRahul K Nayak, David Wendler, Franklin G Miller, et al.Journal of Child and Adolescent Psychopharmacology|September 12, 2014
Evaluating the risks of clinical research: direct comparative analysisAnnette Rid, Emily Abdoler, Roxann Roberson-Nay, et al.AJOB Empirical Bioethics|August 22, 2022
Ethical Challenges Experienced by Clinical Ethicists during COVID-19Connie M Ulrich, Janet A Deatrick, Jesse Wool, et al.Medicine, Health Care, and Philosophy|October 17, 2007
Does fear of retaliation deter requests for ethics consultation?Marion Danis, Adrienne Farrar, Christine Grady, et al.Pageof 26