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Sarah E. Keyes, Charlotte L. Clarke & Catherine E. Gibb. (2019) Living with dementia, interdependence and citizenship: narratives of everyday decision-making. Disability & Society 34:2, pages 296-319.
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Kjetil Lundberg. (2018) Dementia Care Work Situated Between Professional and Regulatory Codes of Ethics. Ethics and Social Welfare 12:2, pages 133-146.
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Robert Alcock. (2014) Ian's Story: His Right to Self-determination. Ethics and Social Welfare 8:1, pages 77-85.
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Tula Brannelly, Amohia Boulton & Allie te Hiini. (2013) A Relationship Between the Ethics of Care and Māori Worldview—The Place of Relationality and Care in Maori Mental Health Service Provision. Ethics and Social Welfare 7:4, pages 410-422.
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Articles from other publishers (16)
Donny H.Y. Li, Marie-Lee Yous, Paulette V. Hunter, Esther Coker, Danielle Just, Vanina Dal Bello-Haas, Carrie McAiney, Abigail Wickson-Griffiths & Sharon Kaasalainen. (2023) Supporting the “hallway residents”: a qualitative descriptive study of staff perspectives on implementing the Namaste Care intervention in long-term care. BMC Geriatrics 23:1.
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Kirstein Rummery. (2022) The right to care? Social citizenship and care poverty in developed welfare states. International Journal of Sociology and Social Policy 43:1/2, pages 33-47.
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Bethan Griffith, Tessa Pollard, Kate Gibson, Jayne Jeffries & Suzanne Moffatt. (2022) Constituting link working through choice and care: An ethnographic account of front‐line social prescribing. Sociology of Health & Illness 45:2, pages 279-297.
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Kellyn Lee. (2021) Inclusion of people with dementia in research can help nurses understand how to deliver successful reminiscence interventions. Evidence Based Nursing 24:3, pages 85-85.
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Xia Li, John Keady & Richard Ward. (2019) Transforming lived places into the connected neighbourhood: a longitudinal narrative study of five couples where one partner has an early diagnosis of dementia. Ageing and Society 41:3, pages 605-627.
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Alex McKeown, Andrew Turner, Zuzanna Angehrn, Dianne Gove, Amanda Ly, Clementine Nordon, Mia Nelson, Claire Tochel, Brent Mittelstadt, Alex Keenan, Michael Smith & Ilina Singh. (2020) Health Outcome Prioritization in Alzheimer’s Disease: Understanding the Ethical Landscape. Journal of Alzheimer's Disease 77:1, pages 339-353.
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Charlotte L Clarke, Jane Wilcockson, Julie Watson, Heather Wilkinson, Sarah Keyes, Lindsay Kinnaird & Toby Williamson. (2018) Relational care and co-operative endeavour – Reshaping dementia care through participatory secondary data analysis. Dementia 19:4, pages 1151-1172.
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Alisa Grigorovich, Pia Kontos & Alexis P. Kontos. (2019) The “Violent Resident”: A Critical Exploration of the Ethics of Resident-to-Resident Aggression. Journal of Bioethical Inquiry 16:2, pages 173-183.
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Marian Barnes, Flis Henwood & Naomi Smith. (2014) Information and care: A relational approach. Dementia 15:4, pages 510-525.
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Deborah O’Connor & Ann-Charlotte Nedlund. (2016) Editorial introduction: Special issue on Citizenship and Dementia. Dementia 15:3, pages 285-288.
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Clive Baldwin & Michelle Greason. (2016) Micro-citizenship, dementia and long-term care. Dementia 15:3, pages 289-303.
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Kirstein Rummery & Michael Fine. (2012) Care: A Critical Review of Theory, Policy and Practice. Social Policy & Administration 46:3, pages 321-343.
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Julia M. Puaschunder. (2018) Socio-econo-engineering: What Is the Right Dose of Capitalism Regarding Fertility? Recommendations How to Use Capitalism for Population Control and How to Avert the Falling Rate of Fertility in Capitalist Territories. SSRN Electronic Journal.
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