BIOETYKA / WPROWADZENIE

BIBLIOGRAFIA

Abberley, P., The concept of oppression and the development of a social theory of disability, Disability, Handicap & Society 2(1)/1987, s. 5-19

Amundson, R., Disability, ideology, and quality of life. A bias in biomedical ethics [w:] Quality of life and human difference: genetic testing, health care and disability, Wasserman, D., Bickenbach, J., Wachbroit, R. (red.), Cambridge University Press, Cambridge 2005, s. 101-124.

Amundson, R., Tresky, S., On a bioethical challenge to disability rights, Journal of Medicine and Philosophy: A Forum for Bioethics and Philosophy of Medicine 32(6)/2007, s. 541-561.

Barnes, C., Disabled people in Britain and discrimination: a case for anti-discrimination legislation, Hurst/BCODP, London 1991;

Barnes, C., Mercer, G., Disability, Polity, Oxford 2003.

Barnes, E., The minority body: a theory of disability, Oxford University Press, Oxford 2016.

Barnes, E., Valuing disability, causing disability, Ethics 125(1)/2014, s. 88-113.

Buchanan, A., Brock, D., Daniels, N., Winkler, D., From chance to choice: genetics and justice, Oxford University Press, Oxford 2000.

Campbell, S., Stramondo, J., The complicated relationship of disability and well-being, Kennedy Institute of Ethics Journal 27/2017, s. 151-184.

Daniels, N., Equality of what: welfare, resource, or capabilities?, Philosophy and Phenomenological Research 50/1990, s. 273-296.

Degener, T., A new human rights model of disability [w:] The United Nations Convention on the Rights of Persons with Disabilities, Della Fina, V., Cera, R., Palmisano, G. (red.), Springer, Cham 2017, s. 41-59.

Dryla, O., Pojęcie upośledzenia, Principia 60/2014, s. 257-278.

Finkelstein, V., A personal journey into disability politics, Centre for Disability Studies, Leeds 2001.

Finkelstein, V., The social model repossessed, Centre for Disability Studies, Leeds 2001.

Galewicz, W., Dobro i sprawiedliwość w opiece zdrowotnej, Wydawnictwo Uniwersytetu Jagiellońskiego, Kraków 2018.

Gleeson, B., Geographies of disability, Routledge, London 1999.

Glover, J., Choosing children: genes, disability and design, Oxford University Press, Oxford 2008, s. 8.

Harris, J., Is gene therapy a form of eugenics, Bioethics 7/1993, s. 178-187.

Harris, J., Is there a coherent social conception of disability?, Journal of Medical Ethics 26(2)/2000, s. 95-100.

Kahane, G., Savulescu, J., The welfarist account of disability [w:] Disability and disadvantage, K, Brownlee, A. Cureton (red.), Oxford University Press, Oxford 2009, s. 14-53.

Kayess, R., French, P., Out of Darkness into light? Introducing the Convention on the Rights of Persons with Disabilities, Human Rights Law Review 8(1)/2008, s. 1-34.

Oliver, M., Defining impairment and disability: issues at stake, [w:] Exploring the divide, The Disability Press, Leeds 1996, s. 29-54.

Oliver, M., The politics of disablement, Palgrave Macmillan, London 1990;

Oliver, M., Understanding disability: from theory to practice, Palgrave Macmillan, Basingstoke 1996.

Parfit, D., Racje i osoby, Wydawnictwo PWN, Warszawa 2012.

Reindal, S., Disability gene therapy – a challenge to John Harris, Journal of Medical Ethics 26(2)/2000, s. 89-94.

Shakespeare, T, Watson, N., The social model of disability: an outdated ideology?, Research in Social Science and Disability 2/2002, s. 9-28.

Shakespeare, T., Disability rights and wrongs, Routledge, New York 2006.

Silvers, A., An essay on modeling: the social model of disability [w:] Philosophical reflections on disability, Ralston, D., Ho, J. (red.), Springer, London 2010, s. 19-36.

Silvers, A., On the possibility and desirability of constructing a neutral conception of disability, Theoretical Medicine and Bioethics 24(6)/2003, s. 471-487.

Swain, J., French, S., Towards an affirmation model of disability, Disability & Society 15(4)/2000, s. 569-582.

Thomas, C., How is disability understood? An examination of sociological approach, Disability & Society 19(6)/2004, s. 569-583.

Thomas, C., Rescuing a social relational understanding of disability, Scandinavian Journal of Disability Research 6(1)/2004, s. 22-36.

Traustadottir, R., Disability studies, the social model and legal developments, [w:] The UN Convention on the Rights of Persons with Disabilities, Nijhoff, Leiden 2009, s. 1-16.

Wasserman, D., Asch, A., Disabilities, people with [w:] International Encyclopedia of ethics, H. Lafolette (red.), Wiley-Blackwell, Chicester 2013.

Wasserman, D., Some moral issues in the correction of impairments, Journal of Social Philosophy 27(2)/1996, s. 128-145.

Watson, N., Well, I know this is going to sound very strange to you, but I don’t see myself as a disabled person: identity and disability, Disability & Society 17(5)/2002, s. 509-528.

Wendell, S., The rejected body. Feminist philosophical reflections on disability, Routledge, New York 1996.

Williams, S., Is anybody there? Critical realism, chronic illness and the disability debate, Sociology of Health and Illness 21(6)/1999, s. 797-819.