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BMC Medical Ethics|July 17, 2016
Readability of patient information and consent documents in rheumatological studiesBente Hamnes, Yvonne van Eijk-Hustings, Jette PrimdahlBMC Medical Ethics|July 28, 2016
Dying well with reduced agency: a scoping review and thematic synthesis of the decision-making process in dementia, traumatic brain injury and frailtyGiles Birchley, Kerry Jones, Richard Huxtable, et al.BMC Medical Ethics|August 25, 2025
Public trust of AI in healthcare in South Africa: results of a surveyDonrich Thaldar, Dane BottomleyBMC Medical Ethics|August 17, 2016
A survey of patient perspectives on the research use of health information and biospecimensStacey A Page, Kiran Pohar Manhas, Daniel A MuruveBMC Medical Ethics|August 23, 2025
Motivations, acceptability and ethical considerations for interventional HIV cure research at the end of life: perspectives from long-term survivors of HIV in the United StatesAli Ahmed, Jeff Taylor, Whitney Tran, et al.BMC Medical Ethics|July 25, 2016
Bioethics education in clinical settings: theory and practice of the dilemma method of moral case deliberationMargreet Stolper, Bert Molewijk, Guy WiddershovenBMC Medical Ethics|May 11, 2021
Taking stock of the availability and functions of National Ethics Committees worldwidePatrik Hummel, Taghreed Adam, Andreas Reis, et al.BMC Medical Ethics|August 15, 2021
South African traditional values and beliefs regarding informed consent and limitations of the principle of respect for autonomy in African communities: a cross-cultural qualitative studyFrancis Akpa-Inyang, Sylvester C ChimaBMC Medical Ethics|May 14, 2021
Cultural sensitivity in brain death determination: a necessity in end-of-life decisions in JapanYuri Terunuma, Bryan J MathisBMC Medical Ethics|May 18, 2021
On intimate relationships between healthcare professionals and patients: a nationwide cohort analysis of medical tribunal decisions in the NetherlandsWim Rietdijk, Sander RenesPageof 175