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BMC Medical Ethics|December 9, 2022
Assent, parental consent and reconsent for health research in Africa: thematic analysis of national guidelines and lessons from the SickleInAfrica registryNchangwi Syntia Munung, Victoria Nembaware, Lawrence Osei-Tutu, et al.BMC Medical Ethics|May 7, 2022
"Many roads lead to Rome and the Artificial Intelligence only shows me one road": an interview study on physician attitudes regarding the implementation of computerised clinical decision support systemsDaan Van Cauwenberge, Wim Van Biesen, Johan Decruyenaere, et al.BMC Medical Ethics|December 10, 2022
Is there a civic duty to support medical AI development by sharing electronic health records?Sebastian MüllerBMC Medical Ethics|October 17, 2020
Forgoing life-sustaining treatment - a comparative analysis of regulations in Japan, Korea, Taiwan, and EnglandMiho Tanaka, Satoshi Kodama, Ilhak Lee, et al.BMC Medical Ethics|October 22, 2020
Genetic testing for breast cancer risk, from BRCA1/2 to a seven gene panel: an ethical analysisErik Gustavsson, Giovanni Galvis, Niklas JuthBMC Medical Ethics|February 1, 2020
Addressing harm in moral case deliberation: the views and experiences of facilitatorsBenita Spronk, Guy Widdershoven, Hans AlmaBMC Medical Ethics|January 18, 2020
Do patients and research subjects have a right to receive their genomic raw data? An ethical and legal analysisChristoph Schickhardt, Henrike Fleischer, Eva C WinklerBMC Medical Ethics|July 14, 2021
Pushing poverty off limits: quality improvement and the architecture of healthcare valuesPolly Mitchell, Alan Cribb, Vikki Entwistle, et al.BMC Medical Ethics|July 14, 2021
Non-medical risk factors associated with postponing elective surgery: a prospective observational studyJulia Becker, Gerald Huschak, Hannes-Caspar Petzold, et al.BMC Medical Ethics|May 29, 2021
Stakeholders' perspectives on research integrity training practices: a qualitative studyDaniel Pizzolato, Kris DierickxPageof 175