| 參考文獻 |
參考文獻
一. 中文文獻
(一) 專書
李瑞全 (1990)，《儒家生命倫理學》，台北：鵝湖出版社。
李瑞全、蔡篤堅編 (2003)，《基因治療、法律、社會意涵論文選集》，台北市：唐山出版社。
賴美渝 (2007)，《實施基因治療之法律問題》，台北：世新大學法律學系碩士論文。
邱格屏 (2009)，《人類基因的權利研究》，北京：法律出版社。
衛生署 (2002)，《基因治療人體試驗申請與操作規範》。
戴華、袁世敏等策劃 (2004)，《美麗新世界的誘惑 - - 基因科技與人文的對話》，台北市：時報文教基金會。
(二)單篇與期刊論文
林志六 (2000)，〈種系細胞基因治療的倫理問題〉，《生物科技與法律研究通訊》，台北：台大法研所，4月，第六期。
李瑞全 (1998)，〈從儒家視域看人類基因圖組研究計劃〉，《應用倫理學研究通訊》， 中壢：中央大學哲研所，4月，第七期。
(2003)，〈基因疾病、基因治療與醫療保健〉，收錄於李瑞全等編，《基因治療、法律、社會意涵論文選集》，台北市：唐山出版社，頁29-56。
(2007)，〈台灣健保制度之公平性：一個初步分析〉，《中國自然辯證法研究會：醫學與哲學(人文社會醫學版)》，第12期，
吳全峰 (2009)，〈健康照護資源分配之界線 - - 兼論醫療科技發展下健康照護資源分配之變與不變〉，《2009科技發展與法律規範雙年刊》(台北：中央研究院法律學研究所籌備處，民國99年5月)，頁299-367。
吳秀瑾 (2001)，〈基因知識、倫理觀與生物決定論〉，收錄於《基因大狂潮》，台北：牛頓雜誌。
陳瑤華 (2003) ，〈完美的Baby？ - - 胎兒基因篩檢的女性主義立場〉，收錄於李 瑞全、蔡篤堅編《基因治療與倫理、法律、社會意涵倫文選集》，台北市：唐山出版社，，頁93-124。
黃默、陳宏銘 (2003)，〈基因革命的政治意涵 - - 以基因測試與治療為例〉，收錄於李瑞全、蔡篤堅編《基因治療與倫理、法律、社會意涵倫文選集》，台北市：唐山出版社，，頁177-187。
蔡甫昌 (2001)，〈基因治療的倫理省思〉，《應用倫理研究通訊》，中壢：中央大學，4月，第18期。
鐘芳樺和何建志譯 (1997)，〈對某些女性主義者質疑產前診斷的批評〉，《生物科技與法律研究通訊》，台北：台大法研所，7月，第三期，頁15-16。
二. 外文文獻
(一)專書
Barry, Brian (1973). The Liberal Theory of Justice. Oxford: Oxford University Press.
(1989). Theories of Justice. California : University of California Press.
Beauchamp, L. Tom & James M. Childress (1994) Principles of Biomedical Ethics 4th edition. Oxford: Oxford University Press.
Beauchamp, L. Tom & LeRoy Walters (2003). Contemporary Issues in Bioethics 6th edition. Belmont, CA: Wadsworth.
Buchanan, Allen & Dan W. Brock & Normen Daniels & Daniel Wikler (2000). From Chance to Choice: Genetics and Justice. Cambridge: Cambridge University Press.
Daniels, Norman (1985). Just Health Care. Cambridge: Cambridge University Press.
(2008). Just Health: Meeting Health Needs Fairly. New York: Cambridge University Press .
Dworkin, Ronald (1977). Taking Rights Seriously. London: Duckworth.
(1985). A Matter of Principle. London: Harvard University Press.
(2000). Sovereign Virtue: The Theory and Practice of Equality. MA: Harvard University Press.
Engelhardt, H. T Jr. (1996). The Foundations of Bioethics 2th edition. Oxford: Oxford University Press.
European Medicines Agency (2009). Questions and Answers on Gene Therapy
Fan, Ruiping (1999). Social Justice in Health Care: A Critical Appraisal. Ph. D. Dissertation, Rice University.
FDA (2002). Guidance for Industry.
Hamilton, Edith & Huntington Cairns (1961). The Collected Dialogues of Plato, Including the Letters. New York: Pantheon Books.
Hayek, A. Friedrich (1976). Law, Legislation and Liberty. Chicago: Unoversity of Chicago Press.
Kevles, J. Daniel (1997). In The Name of Eugenics. Cambridge: Harvard University Press.
Kymlicka, Will (2001). Contemporary Political Philosophy: An Introduction. Oxford: Oxford University Press.
Lee, Shui Chuen (ed) (2007). The Family, Medical Decision-Making, and Biotechnology: Critical Reflections on Asian Moral Perspectives. Dordrecht: Springer, Kluwer Academic Publishers.
MacIntyre, Alasdair (1984). After Virtue: Astudy in Moral Theory. Indiana: University of Notre Dame.
Marshall, T. H. (1965). Class, Citizenship and Social Development. New York: Anchor.
Nozick, Robert (1974), Anarchy, State, and Utopia. New York: Basic Books.
Proctor, Robert (1988). Racial Hygiene: Medicine under the Nazis. Cambridge, MA: Harvard University Press.
Proposed International Guidelines on Ethical Issues in Medical Gentics and Gentic Services (1998). World Health Organization.
Rawls, John (1971). A Theory of Justice. Cambridge: Harvard University Press.
(1993). Political Liberalism. New York: Columbia University Press.
(2001). Justice as Fairness. Cambridge: Harvard University Press.
Rolston, Holmes (1988). Environmental Ethics: Duties to and Values in the Natural World. Philadephia: Temple University Press.
Sen, Amartya (1992). Inequality Reexamined. Cambridge, MA: Harvard University Press.
Singer, Peter (1993). Practice Ethics 2th edition. Cambridge: Cambridge University Press.
(1995). Animal Liberation. London: Pimlico.
Spallone, Patricia (1989). Beyond Conception. MA: Bergin & Garvey Publishers.
Walters, L. & Palmer, J. C. (1997). The ethics of human gene therapy. New York: Oxford University Press.
Wolpert, Lewis (1991). The Triumph of the Embryo. Oxford: Oxford University Press.
Veatch, M. Robert (1986). The Foundation of Justice: Why the Retarded and the Rest of Us Have Claims to Equality. New York: Oxford University Press.
(二)單篇與期刊論文
Andrews, B. Lori (2002). “The Gene Patent Dilemma: Balancing Commercial Incentives with Health Needs” in Houston Journal of Health Law & Policy 2: 65-102.
Arneson, Richard (1989). “Equality and Equal Opportunity for Welfare” in Philosophical Studies 56.
Arras, John (1999). “Getting down to Cases: The Revival of Casuistry in Bioethics” in J. L. Nelson & H. L. Nelson, Meaning and Mediecine: A Reader in Philosophy of Health Care. New York: Routledge.
Berger, M. Edward (1996). “Ethics of Gene Therapy” in Nancy E. Bartlett (eds.), Morality and the New Genetics. MA: Jones and Bartlett Publishers, pp.214-215.
Björkman, B. ; S O Hansson (2006). “Bodily Rights and Property Rights” in Journal of Medical Ethics 32(4): 209-214.
Boorse, Christopher (1997). “Health as a Theoretical Concept” in Philosophy of Science, 44: 542-573.
Buchanan, Allen (1984). “The Right to a Decent Minimum of Health Care” in Tom L. Beauchamp & Leroy Walters (eds.), Contemporary issues in Bioethics. CA: Wadsworth Publishing Company, pp.59-64.
Cohen, G. A. (1986). “Self-Ownership, World-Ownership, and Equality” in F. Lucash (ed.), Justice and Equality: Here and Now. Now York: Cornell University Press, pp.108-135.
Conley, JM ; AK. Doerr; DB. Vorhaus (2010). “Enabling Responsible Public Genomics” in HEALTH MATRIX Clevel 20(2): 325-385.
Culver, M. Charles (1996). “The Concept of Genetic Malady” in Bernard Gert (ed.), Morality and the New Genetics. Boston: Jones and Bartlett Publishers.
Daniels, Norman (1991). “Technology and Resource Allocation: Old Problems in New Clothes”, in South California Law Review 65.
(1994). “The Genome Project, Individual Differences, and Just Health Care”, in T. Murphy & M. Lappe (eds.), Justice and the Huamn Genome Project. Berkeley: University of California Press, pp.111-131.
Dworkin, Ronald (1981). “What is Equality? Part II: Equality of Resources” in Philosophy and Public Affairs, 10 3/4.
Engelhardt, H. T. Jr. (1998). “The obligation of developing human germline genetic engineering: Approaching the future with prudence”，發表於中央大學哲研所和南華大學哲研所合辦之「第一屆生命倫理學國際會議」。中壢與嘉義，6月16-19日。
(1998). “Human Nature Genetically Re-Engineered: Moral Responsbilities To Future Generation” in Emmanuel Agius and Salvino Busuttil (eds.), Germ-line Intervention and our Responsibilities to Future Generations. Netherland: Kluwer Academic Publishers.
“Gene Therapy” (2010). in Insidesalk, February, pp.4-11.
Glover, Jonathan (1999). “Questions about Some Uses of Genetics” in Tom L. Beauchamp & Leroy Walters (eds.), Contemporary Issues in Bioethics. CA: Wadsworth Publishing Company.
Gordon, Ora Karp ; David Lo (2002). “Modern Genetics Reasearch: Will it Change The Practice of Medicine?” in Whitter Law Review 24.
Grand, S. Jeffrey (2002). “The Blooding of America: Privacy and the DNA Dragnet” in Cardozo Law Review 23 (6): 2277-2323.
Herzog, RW. ; Ou Cao ; Arun Srivastava (2010). “Two Decades of Clinical Gene Therapy - Success Is Finally Mounting” in Discovery Medicine 9(45): 105-111.
Hwald, J. Paul (2003). “The Rhetoric of Biopiracy” in Cardozo Journal of International and Comparative Law 11(2): 519-546.
JC, Fletcher & Wertz DC. (1992). “Ethics and prenatal dignosis: Problem, positions and proposed guidelines” in A. Milunsky & J. Milunsky (eds.), Genetic Disorders and the Fetus. Baltimore: Johns Hopkins University Press, pp.823-857.
Jonsen, R. Albert (1996). “The impact of mapping the Human Genome on the Patient – Physician Relationship” in T. H. Murray, M. A. Rothstein, R. E. Murray (eds.), The Human Genome Project and the Future of Health Care. Bloomington and Indianapolis: Indiana University Press, pp.1-20.
Juengst, E. & L. Walters, (1998). “Gene Therapy” in W. T. Reich (ed.), The ethics of sex and genetics. New York: Simon & Schuster Macmillan, pp.256-263.
Kass, Leon (1997). “Why We Should Ban the Cloning of Human Beings” in Cloning Human Beings. National Bioethics Advisory Committee, pp.50-51.
Katz, G. ; Schweitzer SO. (2010). “Implications of Genetic Testing for Health Policy” in Yale J Health Policy Law Ethics 10(1): 90-134.
Lee, Shui Chuen (2004). “Biotechnology and Responsibility to Future Generations: A Confucian Perspective” in Margaret Sleeboom (ed.). Asian Genomics: Cultural Values and Bioethical Practice. Routledge & Kegan Paul.
Lee, Shui Chuen (2007). “On Relational Autonomy: From Feminist Critique to a Confucian Model for Clinical Practice” in Shui Chuen Lee (ed). The Family, Medical Decision-Making, and Biotechnology: Critical Reflections on Asian Moral Perspectives. Dordrecht: Springer, Kluwer Academic Publishers, pp.83-93.
Lewontin, C. Richard (1997). “Science &C ‘The Demon-Haunted World’: An Exchange” in New York Review of Books March 6, pp.51-52.
Martin, P. (1977). “Golding, Ethical Issues in Biological Engineering”in Robert Hunt & John Artas (ed.), Ethical Issues in Modern Medicine. Palo Alto: Mayfield, pp.70-86.
McCrary, S. V. & W. L. Allen (1994). “The Human Genome Initiative and primary care” in J. F. Monagle & D. C. Thomasma (eds.), Health care ethics: Critical issues. Gaithersburg, Maryland: Aspen.
Nussbaum, C. Matha (2002). “Long-Term Care and Social Justice: A Challenge to Conventional Ideas of the Social Contract”in World Health Organization, Ethical choices in long-term care: what does justice require?
Oriola, A. Taiwo (2002). “Ethical and Legal Issues in Singapore Biomedical Reseach” in Pacific Rim Law and Policy Joura l 11(3) :498-529.
Parens, Erik (1999). “The Goodness of Fragility: On the Prospect of Genetic Technologies Aimed at the Enhancement” in Tom L. Beauchamp & Leroy Walters (eds.), Contemporary Issues in Bioethics. CA: Wadsworth Publishing Company.
Parliamentary Office of Science and Technology (2005). “Gene Therapy” in Postnote, June Nr. 240, pp.1-4.
Proctor, N. Robert (1992). “Genomics and Eugenics: How Fair Is the Comparsion?” in G. J. Annas (ed.), Gene Mapping: Using Law and Ethics as Guides. Oxford: Oxford University Press, pp.57-93.
Puri, Allison (2001). “An International DNA Database: Balancing Hope, Privacy, and Scientific Error” in Boston College International and Comparative Law Review, Spring 24(2): 341-380.
Qui, Renzong (1998). “Germ-line Engineering as the Eugenics of the Future” in Emmanuel Agius and Salvino Busuttil (eds.), Germ-line Intervention and our Responsibilities to Future Generations. Netherland: Kluwer Academic Publishers.
Rawls, John (1982). “Social Unity and Primary Goods” in Amartya Sen & Bernard Williams (eds.), Utilitarianism and Beyond. Cambridge: Cambridge University Press.
Saxton, M. (2000). “Why Members of the Disability Community Oppose Prenatal Diagnosis and Selective Abortion” in E. Parens & A. Asch (eds.), Prenatal Testing and Disability Right. Washington, D. C. : Georgetown University Press, pp.147-164.
Siep, Ludwig (2003). “Normative Aspects of Human Body” in Journal of Medicine and Philosophy, Vol. 28, Nr. 2.
Singer, Peter (1976). “Freedoms and Utilities in the Distribution of Health Care” in Robert M. Veatch & Roy Branson (eds.), Ethics and Health Policy. Cambridge: Ballinger Publishing Company.
Smith, R. Kevin (2004). “Gene Therapy: The Potenial Applicability of Gene Transfer Technology to the Human Germline” in International Journal of Medical Sciences 1(2): pp.76-91.
Stein, M. S. (2008). “Necessity, Not Autonomy” in Texas Law Review See Also 86: 15-21.
Walters, Leroy & J. G. Palmer (1999). “The Ethics Engineering” in Tom L. Beauchamp & Leroy Walters (eds.), Contemporary Issues in Bioethics fitfth edition. Belmont, CA: Wadsworth Publishing Company, pp.573-580.
Walzer, Micaael (1992). The Civil Society Argument in C. Mouffe (ed.), Dimensions of Radical Democracy: Pluralism, Citizenship and Community. London: Routledge, pp.89-107.
Watson, J. D. (1992). “A Personal View of the Project”, in D. J. Kevles & L. Hood (ed.), The Code of Code: Scientific and Social Issues in the Human Genome Project. Cambridge: Havard University Press, pp.164-173.
Veatch, M. Robert (1991). “Justice and the Right to Health Care: An Egalitarian Account” in Tomas J. Bole & William B. Bondeson (eds.), Right to Health Care. Dordrecht: Kluwer Academic Publishers.
Young, E. Frank (1997). “Genteic Therapy”, in John F. Kilner & Rebecca D. Pentz & Frank E. Young (eds.), Genetic Ethics. U. K. : Paternoster Press.
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