- Patient autonomy and withholding information.Melissa Rees - 2023 - Bioethics 37 (3):256-264.details
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The Ontological Foundations for Natural Law Theory and Contemporary Ethical Naturalism.Bernard Mauser - unknowndetails
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Global Bioethics.Heather Widdows, Donna Dickenson & Sirkku Hellsten - 2003 - New Review of Bioethics 1 (1):101-116.details
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Diversity and uniformity in genetic responsibility: moral attitudes of patients, relatives and lay people in Germany and Israel. [REVIEW]Aviad E. Raz & Silke Schicktanz - 2009 - Medicine, Health Care and Philosophy 12 (4):433-442.details
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Communicating genetic information in the family: enriching the debate through the notion of integrity. [REVIEW]Paula Boddington & Maggie Gregory - 2008 - Medicine, Health Care and Philosophy 11 (4):445-454.details
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Predictive Genetic Testing, Autonomy and Responsibility for Future Health.Elisabeth Hildt - 2009 - Medicine Studies 1 (2):143-153.details
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The Right to Know and the Right Not to Know Revisited: Part One.Roger Brownsword & Jeff Wale - 2017 - Asian Bioethics Review 9 (1-2):3-18.details
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Gender Transition: Is There a Right to Be Forgotten?Mónica Correia, Guilhermina Rêgo & Rui Nunes - 2021 - Health Care Analysis 29 (4):283-300.details
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What should we want to know about our future? A Kantian view on predictive genetic testing.Bert Heinrichs - 2005 - Medicine, Health Care and Philosophy 8 (1):29-37.details
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Präimplantationsdiagnostik als Vorbereitung von Screeningprogrammen?Hille Haker - 1999 - Ethik in der Medizin 11 (1):104-114.details
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(1 other version)The Right Not to Know and the Duty to Tell: The Case of Relatives.Niklas Juth - 2014 - Journal of Law, Medicine and Ethics 42 (1):38-52.details
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The logic of the interaction between beneficence and respect for autonomy.Shlomo Cohen - 2019 - Medicine, Health Care and Philosophy 22 (2):297-304.details
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(2 other versions)Please Don’t Tell Me.Jonathan Herring & Charles Foster - 2012 - Cambridge Quarterly of Healthcare Ethics 21 (1):20.details
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(2 other versions)Please Don’t Tell Me.Jonathan Herring & Charles Foster - 2012 - Cambridge Quarterly of Healthcare Ethics 21 (1):20-29.details
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Social-science perspectives on bioethics: Predictive genetic testing (PGT) in asia. [REVIEW]Margaret Sleeboom-Faulkner - 2007 - Journal of Bioethical Inquiry 4 (3):197-206.details
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(1 other version)The relative importance of undesirable truths.Lisa Bortolotti - 2013 - Medicine, Health Care and Philosophy 16 (4):683-690.details
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(1 other version)Bioethical theory and practice in genetic screening for type 1 diabetes.U. Gustafsson Stolt, J. Ludvigsson, P. -E. Liss & T. Svensson - 2003 - Medicine, Health Care and Philosophy 6 (1):45-50.details
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(1 other version)The relative importance of undesirable truths.Lisa Bortolotti - 2012 - Medicine Healthcare and Philosophy (4):683-690.details
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(1 other version)The jurisprudence of genetic privacy.Tony McGleenan - 1998 - Medicine, Health Care and Philosophy 1 (3):225-233.details
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Consent to epistemic interventions: a contribution to the debate on the right (not) to know.Niels Nijsingh - 2016 - Medicine, Health Care and Philosophy 19 (1):103-110.details
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(1 other version)Genetisches Screening und Ethik: Europäische Perspektiven : Ein Bericht über das EUROSCREEN I Projekt. [REVIEW]Ruth Chadwick, Henk ten Have, Jorgen Husted, Mairi Levit, Tony McGleenan, Darren Shickle & Urban Wiesing - 1998 - Ethik in der Medizin 10 (3):195-202.details
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(1 other version)The jurisprudence of genetic privacy.Tony McGleenan - 1998 - Medicine, Health Care and Philosophy 1 (3):225-233.details
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