ISBN: 9783846588819 - genetic information - values and rights: the morality of presymptomatic genetic testing (5 risultati)

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  • Lingua: Inglese

    Editore: LAP LAMBERT Academic Publishing, 2012

    3846588814 / 9783846588819

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    Da: Mispah books, Redhill, SURRE, Regno UnitoMispah books

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    Paperback. Condizione: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

  • Lingua: Inglese

    Editore: LAP LAMBERT Academic Publishing Feb 2012, 2012

    3846588814 / 9783846588819

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    Da: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, GermaniaBuchWeltWeit Ludwig Meier e.K.

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    EUR 79,00

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    Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -This book discusses the moral concerns due to the increasing possibilities to predict individuals health on the basis of genetic testing. To what extent should such testing be performed Which parties should be allowed to gain access to the results of such testing The scope and limits of patients right to know and not know are presented. It is also argued that patients value of presymptomatic genetic testing ultimately rests on autonomy and subjective well-being. Moreover, a conception of autonomy is developed, which is useful to analyse the novel idea in this area that autonomy is a value that should be promoted. Regarding the question of blood relatives rights to genetic information, it is argued that we should generally leave the decision to inform relatives to the tested person. The idea that genetic information belongs to a new paradigm of medical information that is communal in its nature is criticized. Broader societal questions regarding e.g. insurance companies right to genetic information are also discussed. It is argued that the development of genetics strengthens the need for and defence of a comprehensive welfare state. 484 pp. Englisch.…

  • Lingua: Inglese

    Editore: LAP LAMBERT Academic Publishing, 2012

    3846588814 / 9783846588819

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    Da: moluna, Greven, Germaniamoluna

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    Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Juth NiklasNiklas Juth is a senior lecturer and researcher in medical ethics at Karolinska Institutet. His main research interests are in ethics and bioethics, genethics, and the intersection between political philosophy and medical . …

  • Lingua: Inglese

    Editore: LAP LAMBERT Academic Publishing, 2012

    3846588814 / 9783846588819

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    Da: AHA-BUCH GmbH, Einbeck, GermaniaAHA-BUCH GmbH

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    EUR 79,00

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    Taschenbuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - This book discusses the moral concerns due to the increasing possibilities to predict individuals health on the basis of genetic testing. To what extent should such testing be performed Which parties should be allowed to gain access to the results of such testing The scope and limits of patients right to know and not know are presented. It is also argued that patients value of presymptomatic genetic testing ultimately rests on autonomy and subjective well-being. Moreover, a conception of autonomy is developed, which is useful to analyse the novel idea in this area that autonomy is a value that should be promoted. Regarding the question of blood relatives rights to genetic information, it is argued that we should generally leave the decision to inform relatives to the tested person. The idea that genetic information belongs to a new paradigm of medical information that is communal in its nature is criticized. Broader societal questions regarding e.g. insurance companies right to genetic information are also discussed. It is argued that the development of genetics strengthens the need for and defence of a comprehensive welfare state.…

  • Lingua: Inglese

    Editore: LAP LAMBERT Academic Publishing Feb 2012, 2012

    3846588814 / 9783846588819

    • Brossura
    • Print on Demand

    Da: buchversandmimpf2000, Emtmannsberg, BAYE, Germaniabuchversandmimpf2000

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    Condizione: Nuovo

    EUR 79,00

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    Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -This book discusses the moral concerns due to the increasing possibilities to predict individuals' health on the basis of genetic testing. To what extent should such testing be performed Which parties should be allowed to gain access to the results of such testing The scope and limits of patients' right to know and not know are presented. It is also argued that patients' value of presymptomatic genetic testing ultimately rests on autonomy and subjective well-being. Moreover, a conception of autonomy is developed, which is useful to analyse the novel idea in this area that autonomy is a value that should be promoted. Regarding the question of blood relatives' rights to genetic information, it is argued that we should generally leave the decision to inform relatives to the tested person. The idea that genetic information belongs to a new paradigm of medical information that is communal in its nature is criticized. Broader societal questions regarding e.g. insurance companies' right to genetic information are also discussed. It is argued that the development of genetics strengthens the need for and defence of a comprehensive welfare state.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 484 pp. Englisch.…