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Journal of Medical Ethics|February 6, 2010
Examining the public refusal to consent to DNA biobanking: empirical data from a Swedish population-based studyPhilippe A Melas, Louise K Sjöholm, Tord Forsner, et al.Journal of Medical Ethics|February 6, 2010
The use of placebo in a trial of rectal artesunate as initial treatment for severe malaria patients en route to referral clinics: ethical issuesAndrew Kitua, Peter Folb, Marian Warsame, et al.Journal of Medical Ethics|May 5, 2018
A threshold of significant harm (f)or a viable alternative therapeutic option?Jo BridgemanJournal of Medical Ethics|August 5, 2018
What are we to make of the charge that human biological enhancement technologies are 'unnatural'?Paul Richard MillerJournal of Medical Ethics|August 2, 2018
Within the limits of the defensible: a response to Simkulet's argument against the pro-life view on the basis of spontaneous abortionHenrik Friberg-FernrosJournal of Medical Ethics|April 26, 2017
Professional and conscience-based refusals: the case of the psychiatrist's harmful prescriptionMorten MagelssenJournal of Medical Ethics|April 29, 2017
Pathways to genetic parenthood for same-sex couplesTimothy F MurphyJournal of Medical Ethics|March 10, 2010
The cost of autonomy: estimates from recent advances in living donor kidney transplantationPhedias DiamandisJournal of Medical Ethics|April 27, 2018
Healthcare professionals' understanding of the legislation governing research involving adults lacking mental capacity in England and Wales: a national surveyVictoria Shepherd, Richard Griffith, Mark Sheehan, et al.Pageof 471