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題名:論建置生物資料庫之關係自律與知情同意原則
書刊名:神學與教會
作者:陳文珊
出版日期:2009
卷期:34:1
頁次:頁296-319
主題關鍵詞:自律關係自律知情同意能力
原始連結:連回原系統網址new window
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  • 被引用次數被引用次數:期刊(0) 博士論文(0) 專書(0) 專書論文(0)
  • 排除自我引用排除自我引用:0
  • 共同引用共同引用:56
  • 點閱點閱:46
期刊論文
1.Dickenson, Donna(2004)。Consent, Commodification and Benefit-Sharing in Genetic Research。Developing World Bioethics,4(2),109-124。  new window
2.Allen, Jay M.(1991)。Am I My Parents, Keeper? An Essay on Justice Between The Young and The Old。Brigham Young University Law Review,1,587-601。  new window
3.Amsperger, Christian、Varoufakis, Yanis(2003)。Toward a Theory of Solidarity。Erkenntnis,59,157-188。  new window
4.Bovenberg, Jasoer A.(200512)。Towards an International System of Ethics and Goverance of Biobanks: A Special Status for Genetic Data?。Critical Public Health,15(4),369-383。  new window
5.Cahill, Lisa。Sowle Genetics, Commodification, and Social Justice in the Globalization Era。Kennedy Institute of Ethics Journal,11(3),221-238。  new window
6.DeCamp, Mathew、Sugarman, Jeremy(2004)。Ethics in Population-based Genetic Research。Accountability in Research,11,1-26。  new window
7.Dickenson, Donna(2002)。Commodification of Human Tissue: Implications for Feminist and Development Ethics。Developing World Bioethics,2(1)。  new window
8.Harris, John(1999)。Ethical Genetic Research on Human Subjects。Jurimetrics J.,40,77-91。  new window
9.Hoeyer, Klaus(200212)。Lindgaard, Conflicting Notions of Personhood in Genetic Research。Anthroppology Today,18(5)。  new window
10.Kegley, Jacquelyn Ann K.(2004)。Challenges to Informed Consent。EMBO Reports,5(9)。  new window
11.Kottow, M.(2004)。The battering of informed consent。J Med Ethics,30(6),565-569。  new window
12.Levitt, Mairi、Weldon, Sue(200512)。A Well Placed Trust?: Public Perceptions of the Governance of DNA Databases。Critical Public Health,15(4),311-321。  new window
13.Macklin, Ruth(1999)。Understanding Informed Consent。Acta Oncologica,38(1),83-87。  new window
14.Palsson, Gisli(2002)。The Life of Family Trees and the Book of Icelanders。Medical Anthropology,21,337-367。  new window
15.Racine, Eric(2003)。Discourse Ethics as an Ethics of Responsibility: Comparison and Evaluation of Citizen Involvement in Population Genomics。Journal of Law, Medicine and Ethics,31,390-397。  new window
16.Sachs, Lisbeth(2004)。The New Age of The Molecular Family: An Anthropological View on the Medicalisation of Kinship。V Scand J Public Health,32,24-29。  new window
17.Tutton, Richard(2002)。Gift relationships in Genetics Research。Science as Culture,11(4)。  new window
18.Winickoff, David E.、Winickoff, Richard N.。The Charitable Trust as a Model for Genomic Biobanks。N. Eng. J Med,349,12。  new window
19.Winickoff, David E.、Neumann, Larissa B.(2005)。Towards a Social Contract for Genomics: Property and the public in the ‘Biotrust’ Model。Genomics, Society and Policy,1(3)。  new window
20.Witte, Joke I. De、Have, Henk(1997)。Ten Ownership of Genetic Material and Information。Soc. Sci. Med.,45(1),51-60。  new window
21.Kaiser, Jocelyn(1158)。Population Databases Boom, from Iceland to the U.S.。Science,298,1158。  new window
22.Boggio, Andrea(2005)。Charitable Trusts and Human Research Genetic Databases: The Way Forward?。Genomics, Society and Policy,1(2),41-49。  new window
23.Safrin, Sabrina(2004)。Hyperownership in a Time of Bioetchnological Promise: The International Conflict to Control the Building Blocks of Life。The American Journal of International Law,98(4),641-685。  new window
24.劉宏恩(20040600)。冰島設立全民醫療及基因資料庫之法律政策評析--論其經驗及爭議對我國之啟示。臺北大學法學論叢,54,41-43+45-99。new window  延伸查詢new window
25.Greely, Henry T.(2001)。Informed Consent and Other Ethical Issues in Human Population Genetics。Annu. Rev. Genet,35,785-800。  new window
會議論文
1.Boggio, Andrea(2004)。The Capability Approach in Genetic Research: Mediating Individualism and Solidarity。4th International Conference on the Capability Approach,(會議日期: 2004/09/05-09/07)。Italy:University of Pavia。  new window
2.Harris, John(2003)。Scientific Research Is a Moral Duty。第四屆台灣生命倫理學學術研討會,國立中央大學哲學研究所 。  延伸查詢new window
3.中央研究院人文社會科學研究中心、調査研究專題中心、台灣ELSI研究中心(2006)。「台灣基因意向之調査與研究」學術研討會會議論文集。  延伸查詢new window
圖書
1.Alnes, Anne Hambro(20041009)。‘We Want Your Tape’: An Anthropologist View on Biobank。Toulouse。  new window
2.Daniels, Norman(1988)。Am I My Parents' Keeper? An Essay on Justice Between The Young and The Old。New York:Oxford University Press。  new window
3.Hoeyer, Klaus(2004)。Lindgaard, Biobanks and Informed Consent: An Anthropological Contribution to Medical Ethics。Umea:SolQardern Offset AB。  new window
4.霍布士(1984)。利維坦。台北:台灣商務印書館。  延伸查詢new window
5.Titmuss, Richard M.(1970)。The Gift Relationship: From Human Blood to Social Policy。Harmondsworth, UK:London:George Allen and Unwin。  new window
6.林火旺(1997)。倫理學。臺北:國立空中大學。  延伸查詢new window
7.Dawkins, Richard、趙淑妙(1995)。自私的基因。台北:遠見天下文化公司。  延伸查詢new window
8.李瑞全(1999)。儒家生命倫理學。臺北:鵝湖出版社。  延伸查詢new window
9.Mauss, Marcel、汪珍宜、何翠萍(1989)。禮物:舊社會中交換的形式與功能。遠流出版事業股份有限公司。  延伸查詢new window
10.約翰.洛克、葉啟芳(1986)。政府論次講。臺北:唐山。  延伸查詢new window
11.葉保強(20020000)。建構企業的社會契約。臺北:鵝湖。new window  延伸查詢new window
其他
1.Bentar, David。Informed consent and Research,http://bmj.bmjjournals.com/cgi/content/full/316/7136/1008。  new window
2.Caulfield, Timothy。Upshur, Ross EG and Daar, Abdallah DNA Databanks and Consent: A Suggested Policy Option Involving an Authorization Model,http://www.biomedcentral.eom/1472-6939/4/l。  new window
3.Edwards, Kelly A.。Informed Consent,http://depts.washington.edu/bioethx/topics/consent.html。  new window
4.Giggins, Helen,Brankovic, Ljiljana。Ethical and Privacy Issues in Genetic Databases,http://citeseer.ist.psu.edu/correct/735177.html。  new window
5.Heijden, Eline。van der On the Notion of Altruism,http://graywww.kub.nl:2080/greyfiles/few/1994/doc/678.pdf。  new window
圖書論文
1.Fan, Ruiping(1999)。Just Health Care, the Good Life, and Confucianism。Confucian Bioethics。Boston:Kluwer Academic Publishers。  new window
2.Wang, Qingjie(1999)。The Confucian Filial Obligation and Care for Aged Parents。Confucian Bioethics。Boston:Kluwer Academic Publishers。  new window
 
 
 
 
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