Sinossi
This volume is a multidisciplinary and multinational collection of papers on aspects of genetic screening, with special reference to the situation in Europe. Starting from the situation in practice, the book proceeds to examine what lessons, if any, can be learned from historical precedents and sociological perspectives and concludes by exploring the extent to which theoretical ethical frameworks can assist in addressing the practice and policy issues in screening. This exploration points to ways in which genetics itself affects and challenge those frameworks. This collection will be of interest to practitioners, ethicists and policy-makers alike.
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Contenuti
Contributors. Preface. The Wilson and Jungner Principles of Screening and Genetic Testing; D. Shickle. Genetic screening, information and counselling in Austria; G. Hauser.The Belgian perspective on genetic screening; K. Dierickx. Thalassemia prevention in Cyprus. Past, present and future; P. Ioannou. Some developments in genetic screening in Finland; V. Launis. Genetic screening: Ethical debates and regulatory systems in France; A. Boué. Screening in Germany: Carrier screening, pre-natal care and other screening projects; T. Schroeder-Kurth. Population screening in Greece for prevention of genetic diseases; C. Metaxotou, A. Mavrou. Ethics and genetic screening in the Republic of Ireland; D. Dooley. Genetic screening in the Netherlands. The state of the debate; R. Hoedemaekers. Genetic screening and genetic services in Slovakia; V. Ferak. Historical and social background. Introduction; H. ten Have. From eugenics to genetic screening. Historical problems of human genetic applications; H.-P. Kröner. Genetics in Germany. History and hysteria; U. Wiesing. A sociological perspective on genetic screening; M. Levitt. Moral and philosophical issues. Introduction; R.F. Chadwick, U. Wiesing. Genetic information and care; I. Pörn. Genetic screening, genetic testing and privacy; J. Sandor. Reconciling liberty and the common good? Genetic screening in the Republic of Ireland; D. Dooley. Genetic screening and testing. A moral map; R. Hoedemaekers. The genetic testing of children; A. Clarke. Index.
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The Ethics of Genetic Screening (Library of Medical Ethics and Theoretical Medicine)
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Buch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -This collection of essays represents the work produced in the course of a three-year project funded by the Commission of the European Communities under the Biomed I programme, on the ethics of genetic screening, entitled 'Genetic screening: ethical and philosophical perspectives, with special reference to multifactorial diseases'. The short title of the project was Euroscreen, thereafter known as Euroscreen I, in the light of the fact that a second project on genetic screening was subsequently funded. The project was multinational and multidisciplinary, and had as its objectives to examine the nature and extent of genetic screening programmes in different European countries; to analyse the social policy response to these developments in different countries; and to explore the applicability of normative ethical frameworks to the issues. The project was led by a core group who had oversight of the project and members of which have acted as editors for this volume. Darren Shickle edited the first section; Henk ten Have the second; Ruth Chadwick and Urban Wiesing the third and final part. The volume opens with an overview of genetic screening and the principles available for addressing developments in the field, with special reference to the Wilson and Jungner principles on screening. The first of the three major sections thereafter includes papers on the state of the art in different countries, together with some analysis of social context and policy. 272 pp. Englisch. Codice articolo 9780792356141
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Gebunden. Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. This collection of essays represents the work produced in the course of a three-year project funded by the Commission of the European Communities under the Biomed I programme, on the ethics of genetic screening, entitled Genetic screening: ethical and phil. Codice articolo 5968786
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Buch. Condizione: Neu. The Ethics of Genetic Screening | Ruth F. Chadwick (u. a.) | Buch | Einband - fest (Hardcover) | Englisch | 1999 | Springer Netherland | EAN 9780792356141 | Verantwortliche Person für die EU: Springer Netherlands, Haberstr. 7, 69126 Heidelberg, buchhandel-buch[at]springer[dot]com | Anbieter: preigu Print on Demand. Codice articolo 102700262
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Condizione: New. This volume is a multidisciplinary and multinational collection of papers on aspects of genetic screening, with special reference to the situation in Europe. Starting from the situation in practice, the book proceeds to examine what lessons, if any, can be learned from historical precedents. Editor(s): Chadwick, Professor Ruth; Shickle, Darren; Have, H. A. Ten; Wiesing, Urban. Series: Library of medical ethics & theoretical medicine. Num Pages: 256 pages, biography. BIC Classification: 1D; MBDC. Category: (P) Professional & Vocational. Dimension: 234 x 156 x 15. Weight in Grams: 559. . 1999. Hardback. . . . . Codice articolo V9780792356141
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Buch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -This collection of essays represents the work produced in the course of a three-year project funded by the Commission of the European Communities under the Biomed I programme, on the ethics of genetic screening, entitled 'Genetic screening: ethical and philosophical perspectives, with special reference to multifactorial diseases'. The short title of the project was Euroscreen, thereafter known as Euroscreen I, in the light of the fact that a second project on genetic screening was subsequently funded. The project was multinational and multidisciplinary, and had as its objectives to examine the nature and extent of genetic screening programmes in different European countries; to analyse the social policy response to these developments in different countries; and to explore the applicability of normative ethical frameworks to the issues. The project was led by a core group who had oversight of the project and members of which have acted as editors for this volume. Darren Shickle edited the first section; Henk ten Have the second; Ruth Chadwick and Urban Wiesing the third and final part. The volume opens with an overview of genetic screening and the principles available for addressing developments in the field, with special reference to the Wilson and Jungner principles on screening. The first of the three major sections thereafter includes papers on the state of the art in different countries, together with some analysis of social context and policy.Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg 272 pp. Englisch. Codice articolo 9780792356141
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Buch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - This collection of essays represents the work produced in the course of a three-year project funded by the Commission of the European Communities under the Biomed I programme, on the ethics of genetic screening, entitled 'Genetic screening: ethical and philosophical perspectives, with special reference to multifactorial diseases'. The short title of the project was Euroscreen, thereafter known as Euroscreen I, in the light of the fact that a second project on genetic screening was subsequently funded. The project was multinational and multidisciplinary, and had as its objectives to examine the nature and extent of genetic screening programmes in different European countries; to analyse the social policy response to these developments in different countries; and to explore the applicability of normative ethical frameworks to the issues. The project was led by a core group who had oversight of the project and members of which have acted as editors for this volume. Darren Shickle edited the first section; Henk ten Have the second; Ruth Chadwick and Urban Wiesing the third and final part. The volume opens with an overview of genetic screening and the principles available for addressing developments in the field, with special reference to the Wilson and Jungner principles on screening. The first of the three major sections thereafter includes papers on the state of the art in different countries, together with some analysis of social context and policy. Codice articolo 9780792356141
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