Books on the topic 'Medical screening Moral and ethical aspects'

Fischer, Michael W., and Markus Hengstschläger. Genetic screening. Frankfurt am Main: Peter Lang, 2009.

Haker, Hille. Ethik der genetischen Frühdiagnostik: Sozialethische Reflexionen zur Verantwortung am Beginn des menschlichen Lebens. Paderborn: Mentis, 2002.

Juth, Niklas. Genetic information values and rights: The morality of presymptomatic genetic testing. Göteburg: Acta Universitatis Gothoburgensis, 2005.

Bellino, Raffaello Maria. Critica della ragione predittiva: L'etica tra scienza e nescienza. Bari: Levante, 2004.

Zakharov, I. A. GenEtika, ili, Rozhatʹ, nelʹzi︠a︡ klonirovatʹ. Novosibirsk: Izd-vo SO RAN, 2003.

Christian, Munthe, and SpringerLink (Online service), eds. The Ethics of Screening in Health Care and Medicine: Serving Society or Serving the Patient? Dordrecht: Springer Science+Business Media B.V., 2012.

Kollek, Regine. Der medizinische Blick in die Zukunft: Gesellschaftliche Implikationen prädiktiver Gentests. Frankfurt am Main: Campus, 2008.

Conference, CIOMS. Genetics, ethics, and human values: Human genome mapping, genetic screening, and gene therapy : proceedings of the XXIVth CIOMS Conference, Tokyo and Inuyama City, Japan, 22-27 July 1990. Geneva: Council for International Organizations of Medical Sciences, 1991.

Leuzinger-Bohleber, Marianne. The Janus face of prenatal diagnostics: A European study bridging ethics, psychoanalysis, and medicine. London: Karnac, 2008.

1959-, Rehmann-Sutter Christoph, and Müller Hj, eds. Disclosure dilemmas: Ethics of genetic prognosis after the 'right to know/not to know' debate. Burlington, VT: Ashgate Pub., 2009.

Louhiala, Pekka. Preventing intellectual disability: Ethical and clinical issues. Cambridge, UK: Cambridge University Press, 2004.

Great Britain. Human Genetics Advisory Commission. The implications of genetic testing for employment. London: Human Genetics Advisory Commission, 1999.

1969-, Bennett Rebecca, and Erin Charles A, eds. HIV and AIDS: Testing, screening, and confidentiality. Oxford: Oxford University Press, 1999.

Achieving justice in genomic translation: Rethinking the pathway to benefit. Oxford: Oxford University Press, 2011.

Brückl, Daniel. Rechtsfragen zur Verwendung von genetischen Informationen über den Menschen: Ein Beitrag zur rechtlichen Steuerung der Verwendung von Wissen. Berlin: Weissensee, 2001.

Burke, Wylie. Achieving justice in genomic translation: Rethinking the pathway to benefit. Oxford: Oxford University Press, 2011.

Leuzinger-Bohleber, Marianne. The Janus face of prenatal diagnostics: A European study bridging ethics, psychoanalysis, and medicine. London: Karnac, 2008.

J, Annas George, and Elias Sherman, eds. Gene mapping: Using law and ethics as guides. New York: Oxford University Press, 1992.

Dierickx, Kris. Genetisch gezond?: Ethische en sociale aspecten van genetische tests en screenings. Antwerpen: Intersentia, 1999.

Am I my genes?: Confronting fate and family secrets in the age of genetic testing. Oxford: Oxford University Press, 2012.

Onimhawo, John Afiagbokai. Ethical, medical, and legal perspectives on euthanasia. Ibadan, Oyo Sate, Nigeria: Stirling-Horden Publishers, 1999.

Held, Forsyth Elizabeth, ed. Medical dilemmas. New York: Putnam, 1990.

Fletcher, Joseph. The ethics of genetic control: Ending reproductive roulette : artificial insemination, surrogate pregnancy, nonsexual reproduction, genetic control and screening. Buffalo: Prometheus, 1988.

Kleinig, John. Ethical issues in psychosurgery. London: Allen & Unwin, 1985.

John, Douard, ed. Ethical practice in clinical medicine. London: Routledge, 1990.

Ellos, William J. Ethical practice in clinical medicine. London: Routledge, 1991.

1956-, Cataldo Peter J., Moraczewski Albert S. 1920-, and Pope John Center Task Force on Human Fetal Tissue Transplantation., eds. The fetal tissue issue: Medical and ethical aspects. Braintree, Mass: Pope John Center, 1994.

Panno, Joseph. Stem cell research: Medical applications and ethical controversies. New York, NY: Facts On File, 2011.

Panno, Joseph. Stem cell research: Medical applications and ethical controversy. New York, NY: Facts On File, 2005.

1952-, Valverde Carlos, ed. Genetic screening of newborns: An ethical inquiry. Hauppauge, N.Y: Nova Science Publishers, 2009.

Marshall, Elizabeth L. Conquering infertility: Medical challenges and moral dilemmas. New York: Franklin Watts, 1997.

Schildmann, Jan. Human medical research: Ethical, legal and socio-cultural aspects. Basel: Springer Verlag, 2012.

Trusting doctors: The decline of moral authority in American medicine. Princeton, NJ: Princeton University Press, 2008.

Without moral limits: Women, reproduction, and the new medical technology. Westchester, Ill: Crossway Books, 1989.

E, Parmet Wendy, ed. Ethical health care. Upper Saddle River, N.J: Pearson/Prentice Hall, 2006.

Ethical decision-making in therapy practice. Oxford: Butterworth-Heinemann, 1997.

Janet, Kelly. Is medical ethics in armed conflict identical to medical ethics in times of peace? Newcastle upon Tyne: Cambridge Scholars Publishing, 2013.

Ekman, Ladd Rosalind, ed. Ethical dilemmas in pediatrics: A case study approach. New York: Springer-Verlag, 1991.

Carlo, Bresciani, ed. Genetica e medicina predittiva: Verso un nuovo modello di medicina? Milano: Giuffrè, 2000.

Juth, Niklas, and Christian Munthe. The Ethics of Screening in Health Care and Medicine: Serving Society or Serving the Patient? Springer, 2013.

1946-, Beck-Gernsheim Elisabeth, ed. Welche Gesundheit wollen wir?: Dilemmata des medizintechnischen Fortschritts. Frankfurt am Main: Suhrkamp, 1995.

Ethik in der Humangenetik. Francke, 2000.

Ethik in der Humangenetik: Die neueren Entwicklungen der genetischen Frühdiagnostik aus ethischer Perspektive. Tübingen: Francke, 1998.

Gastmans, Chris. Between Technology and Humanity: The Impact of Technology on Health Care Ethics. Leuven University Press, 2002.

Marianne, Leuzinger-Bohleber, Engels Eve-Marie, and Tsiantis J, eds. The Janus face of prenatal diagnostics: A European study bridging ethics, psychoanalysis, and medicine. London: Karnac, 2008.

The Janus face of prenatal diagnostics: A European study bridging ethics, psychoanalysis, and medicine. London: Karnac, 2008.

Hecht, Trevor, and Austin F. Maze. Direct-To-Consumer Genetic Tests: Considerations and Questionable Practices. Nova Science Publishers, Incorporated, 2012.

(Editor), Irmgard Nippert, Heidemarie Neitzel (Editor), and Gerhard Wolff (Editor), eds. The New Genetics: From Research into Health Care: Social and Ethical Implications for Users and Providers. Springer, 1999.

(Editor), David Wasserman, Jerome Bickenbach (Editor), and Robert Wachbroit (Editor), eds. Quality of Life and Human Difference: Genetic Testing, Health Care, and Disability (Cambridge Studies in Philosophy and Public Policy). Cambridge University Press, 2005.

T, Wasserman David, Wachbroit Robert Samuel, and Bickenbach Jerome Edmund, eds. Quality of life and human difference: Genetic testing, health care, and disability. Cambridge, UK: Cambridge University Press, 2005.