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  1. To know or not to know? Genetic ignorance, autonomy and paternalism.Jane Wilson - 2005 - Bioethics 19 (5-6):492-504.
    ABSTRACT This paper examines some arguments which deny the existence of an individual right to remain ignorant about genetic information relating to oneself – often referred to as ‘a right to genetic ignorance’ or, more generically, as ‘a right not to know’. Such arguments fall broadly into two categories: 1) those which accept that individuals have a right to remain ignorant in self‐regarding matters, but deny that this right can be extended to genetic ignorance, since such ignorance may be harmful (...)
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  • Ethical issues in tissue banking for research: The prospects and pitfalls of setting international standards.Karen J. Maschke & Thomas H. Murray - 2004 - Theoretical Medicine and Bioethics 25 (2):143-155.
    Bauer, Taub, and Parsi's review of an international sample of standards on informed consent, confidentiality, commercialization, and quality of research in tissue banking reveals that no clear national or international consensus exists for these issues. The authors' response to the lack of uniformity in the meaning, scope, and ethical significance of the policies they examined is to call for the creation of uniform ethical guidelines. This raises questions about whether harmonization should consist of voluntary international standards or international regulations that (...)
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  • Immanuel Kant, his philosophy and medicine.Urban Wiesing - 2007 - Medicine, Health Care and Philosophy 11 (2):221-236.
    The article examines the statements made by Immanuel Kant with reference to medicine as well as the impact of his philosophy on medicine. It describes the initial reaction of Kantian philosophy on medicine in the late 18th and early 19th century and its influence in the late 20th century.
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  • The biogenetical revolution of the Council of Europe- twenty years of the Convention on Human Rights and Biomedicine.Oktawian Nawrot - 2018 - Life Sciences, Society and Policy 14 (1):1-24.
    The Council of Europe’s legal regulation concerning development of biology and medicine undoubtedly form the most interesting, but certainly not perfect, over-national system of protection of human beings in prenatal stages of development. The strength of the mentioned system is that it based on well-known and common acceptable values and rules such as human dignity and its protection. The aim of the paper is to present the reasons behind adopting such a system, as well as the consequences of the latter. (...)
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