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Disability & Society Volume 14, 1999 - Issue 1
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Original Articles

Discriminative Assumptions of Utilitarian Bioethics Regarding Individuals with Intellectual Disabilities

SIMO VEHMAS
Pages 37-52 | Published online: 01 Jul 2010

Citations (24)

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Jonathan Herring. (2022) Sharing Vulnerabilities in the Woman Patient/Doctor Encounter. The New Bioethics 28:3, pages 223-237.
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Guðrún V. Stefánsdóttir & Kristín Björnsdóttir. (2016) ‘I am a college student’ postsecondary education for students with intellectual disabilities. Scandinavian Journal of Disability Research 18:4, pages 328-342.
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Touko Vaahtera. (2016) ‘We swam before we breathed or walked’: able-bodied belonging in popular stories of evolutionary biology. Disability & Society 31:5, pages 591-603.
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Alan Roulstone. (2013) Disability research in the Nordic context – progress and challenges in investment welfare states 1970–2013. Scandinavian Journal of Disability Research 15:sup1, pages 1-12.
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Jonathan Rix. (2009) Statutory assessment of the class? Supporting the additional needs of the learning context. International Journal of Inclusive Education 13:3, pages 253-272.
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Jayne Clapton. (2004) Disability, Ethics, and Biotechnology. Journal of Religion, Disability & Health 8:1-2, pages 21-31.
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Simo Vehmas. (2003) Live and Let Die? Disability in Bioethics. New Review of Bioethics 1:1, pages 145-157.
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Articles from other publishers (17)

Jonathan Herring. (2022) Vulnerability and Children’s Rights. International Journal for the Semiotics of Law - Revue internationale de Sémiotique juridique 36:4, pages 1509-1527.
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James B. Gould. (2022) Why Intellectual Disability is Not Mere Difference. Journal of Bioethical Inquiry 19:3, pages 495-509.
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Owen Barden, Steven J. Walden, Davey Bennett, Nicole Bird, Stella Cairns, Rhiannon Currie, Lynne Evans, Stephen Jackson, Emily Oldnall, Sarah Oldnall, Dawn Price, Tricia Robinson, Amber Tahir, Samantha Taylor, Christine Wright & Claire Wright. (2022) Antonia's story: Bringing the past into the future. British Journal of Learning Disabilities 50:2, pages 258-269.
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James Gould. (2020) The Complicated but Plain Relationship of Intellectual Disability and Well-being. Canadian Journal of Bioethics 3:1, pages 37-51.
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Charles Foster & Jonathan HerringCharles Foster & Jonathan Herring. 2017. Identity, Personhood and the Law. Identity, Personhood and the Law 35 42 .
Heike Felzmann. 2017. Key Concepts and Issues in Nursing Ethics. Key Concepts and Issues in Nursing Ethics 29 41 .
Jonas-Sébastien Beaudry. (2018) The Anxious Heart of Injustice: Negative Affective Responses to Disabilities. BioéthiqueOnline 5.
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Neil McHugh, Rachel M Baker, Helen Mason, Laura Williamson, Job van Exel, Rohan Deogaonkar, Marissa Collins & Cam Donaldson. (2015) Extending life for people with a terminal illness: a moral right and an expensive death? Exploring societal perspectives. BMC Medical Ethics 16:1.
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SØREN HOLM. (2015) The Grand Leap of the Whale up the Niagara Falls. Cambridge Quarterly of Healthcare Ethics 24:2, pages 195-203.
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Kristín Björnsdóttir, Guðrún V Stefánsdóttir & Ástríður Stefánsdóttir. (2014) ‘It’s my life’. Journal of Intellectual Disabilities 19:1, pages 5-21.
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Meir Lotan. 2011. Neurodevelopmental Disabilities. Neurodevelopmental Disabilities 389 417 .
Pekka Louhiala. 2009. Preventing Intellectual Disability. Preventing Intellectual Disability.
J. Clapton. (2003) Tragedy and catastrophe: contentious discourses of ethics and disability. Journal of Intellectual Disability Research 47:7, pages 540-547.
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. 2001. Ethics in Deaf Education. Ethics in Deaf Education 215 225 .
Des Power. 2001. Ethics in Deaf Education. Ethics in Deaf Education 33 45 .
David Turnbull. (2000) Genetic counselling: ethical mediation of eugenic futures?. Futures 32:9-10, pages 853-865.
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Simo Vehmas. (2016) Newborn Infants and the Moral Significance of Intellectual Disabilities. Journal of the Association for Persons with Severe Handicaps 24:2, pages 111-121.
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