18 found
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  1. The Right to Know and the Right Not to Know.Ruth Chadwick, Mairi Levitt & Darren Shickle (eds.) - 2014 - Cambridge University Press.
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  2.  2
    Public Attitudes to Participating in UK BioBank: A DNA Bank, Lifestyle and Morbidity Database on 500,000 Members of the UK Public Aged 45–69. [REVIEW]Darren Shickle, Rhydian Hapgood, Jane Carlisle, Phil Shackley, Ann Morgan & Chris McCabe - 2003 - In Bartha Maria Knoppers (ed.), Populations and Genetics: Legal and Socio-Ethical Perspectives. Martinus Nijhoff.
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  3.  28
    Genetic Screening and Ethics: European Perspectives.Ruth Chadwick, Henk ten Have, Jfrgen Husted, Mairi Levitt, Tony McGleenan, Darren Shickle & Urban Wiesing - 1998 - Journal of Medicine and Philosophy 23 (3):255 – 273.
    Analysis and comparison of genetic screening programs shows that the extent of development of programs varies widely across Europe. Regional variations are due not only to genetic disease patterns but also reflect the novelty of genetic services. In most countries, the focus for genetic screening programs has been pregnant women and newborn children. Newborn children are screened only for disorders which are treatable. Prenatal screening when provided is for conditions for which termination may be offered. The only population screening programs (...)
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  4.  32
    Ethical Models Underpinning Responses to Threats to Public Health: A Comparison of Approaches to Communicable Disease Control in Europe.Sabina Gainotti, Nicola Moran, Carlo Petrini & Darren Shickle - 2008 - Bioethics 22 (9):466-476.
    Increases in international travel and migratory flows have enabled infectious diseases to emerge and spread more rapidly than ever before. Hence, it is increasingly easy for local infectious diseases to become global infectious diseases (GIDs). National governments must be able to react quickly and effectively to GIDs, whether naturally occurring or intentionally instigated by bioterrorism. According to the World Health Organisation, global partnerships are necessary to gather the most up-to-date information and to mobilize resources to tackle GIDs when necessary. Communicable (...)
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  5.  14
    The Consent Problem Within DNA Biobanks.Darren Shickle - 2006 - Studies in History and Philosophy of Science Part C 37 (3):503-519.
    Large prospective biobanks are being established containing DNA, lifestyle and health information in order to study the relationship between diseases, genes and environment. Informed consent is a central component of research ethics protection. Disclosure of information about the research is an essential element of seeking informed consent. Within biobanks, it is not possible at recruitment to describe in detail the information that will subsequently be collected because people will not know which disease they will develop. It will also be difficult (...)
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    The Consent Problem Within DNA Biobanks.Darren Shickle - 2006 - Studies in History and Philosophy of Science Part C: Studies in History and Philosophy of Biological and Biomedical Sciences 37 (3):503-519.
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  7.  24
    Are “Genetic Enhancements” Really Enhancements?Darren Shickle - 2000 - Cambridge Quarterly of Healthcare Ethics 9 (3):342-352.
    The word enhancement is value laden and potentially misleading in the context of genetics. Dictionary definitions of enhance include and The term geneticenhancement would be better replaced with a more neutral term such as to reflect the fact that the consequences of as yet largely untried technology may be beneficial, balanced, or harmful. The aim of this paper is to highlight some of the potential negative consequences of the use of and hence to challenge whether are actually always enhancements. Thus (...)
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  8.  8
    €œOn a Supposed Right to Lie [to the Public] From Benevolent Motives” Communicating Health Risks to the Public.Darren Shickle - 2000 - Medicine, Health Care and Philosophy 3 (3):241-249.
    There are three main categories of rationale for withholding information or telling lies: if overwhelming harm can only be averted through deceit; complete triviality such that it is irrelevant whether the truth is told; a duty to protect the interests of others. Public health authorities are frequently having to form judgements about the public interest, whether to release information or issue warnings. In June 1992, routine surveillance detected patulin levels (a known carcinogen) in samples of apple juice exceeding safety threshold. (...)
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  9.  8
    Euroscreen 2: Zu einer gemeinsamen Versicherungs- und Kommerzialisierungspolitik und zu einer Politik des öffentlichen Bewusstseins über Genetik. [REVIEW]Ruth Chadwick, Henk ten Have, Rogeer Hoedemaekers, Jørgen Husted, Mairi Levitt, Tony McGleenan, Darren Shickle & Urban Wiesing - 2000 - Ethik in der Medizin 12 (4):269-273.
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    Euroscreen 2: Towards Community Policy on Insurance, Commercialization and Public Awareness.Chadwick Ruth, Have Henk ten, Hoedemaekers Rogeer, Husted Jrgen, Levitt Mairi, McGleenan Tony, Shickle Darren & Wiesing Urban - 2001 - Journal of Medicine and Philosophy 26 (3):263-272.
    The project Euroscreen 2 has examined genetic screening and testing with particular reference to implications for insurance, commercialization through marketing of genetic tests direct to the public, and issues surrounding raising public awareness of these and other developments in genetics, including the practical experiment of a Gene Shop. This paper provides a snapshot of the three year project. The study groups work included monitoring developments in different European countries and exploring possibilities for regulation in insurance and commercialization together with public (...)
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  11.  9
    Public Preferences for Health Care: Prioritisation in the United Kingdom.Darren Shickle - 1997 - Bioethics 11 (3-4):277-290.
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    Genetisches Screening und Ethik: Europäische Perspektiven. [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.
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  13. Book Reviews-The Right to Know and the Right Not to Know.Ruth Chadwick, Mairi Levitt, Darren Shickle & Jill Ryan - 1999 - Bioethics 13 (1):84-87.
     
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  14. Genetisches Screening und Ethik: Europische Perspektiven Ein Bericht ber das EUROSCREEN I Projekt.Ruth Chadwick, Henk ten Have, Jorgen Husted, Mairi Levit, Tony McGleenan, Darren Shickle & Urban Wiesing - 1998 - Ethik in der Medizin 3.
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  15. Human Genome Analysis, Genetic Counselling and Ethics.Ruth Chadwick, Henk ten Have, Jørgen Husted, Charles Ngwena, Søren Nørby & Darren Shickle - 1992 - Global Bioethics 5 (4):37-45.
  16. The Right to Know and the Right Not to Know Genetic Privacy and Responsibility.Ruth Chadwick, Mairi Levitt & Darren Shickle (eds.) - 2014 - Cambridge University Press.
     
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  17. The Consent Problem Within DNA Biobanks.Darren Shickle - 2004 - Studies in History and Philosophy of Biological and Biomedical Sciences 37 (3):503-519.
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  18. Euroscreen 2: Zu einer gemeinsamen Versicherungs- und Kommerzialisierungspolitik und zu einer Politik des oeffentlichen Bewusstseins ueber Genetik.Urban Wiesing, Ruth Chadwick, Henk ten Have, Rogeer Hoedemaekers, Joergen Husted, Mairi Levitt, Tony McGleenan & Darren Shickle - 2000 - Ethik in der Medizin 12 (4):269-273.
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