Citations (84)
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Valerie Egdell, Mandy Cook, Jill Stavert, Louise Ritchie, Debbie Tolson & Michael Danson. (2021) Dementia in the workplace: are employers supporting employees living with dementia?. Aging & Mental Health 25:1, pages 134-141.
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Laila Mohrsen Busted, Dorthe S Nielsen & Regner Birkelund. (2020) “Sometimes it feels like thinking in syrup” – the experience of losing sense of self in those with young onset dementia. International Journal of Qualitative Studies on Health and Well-being 15:1.
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Alessandro Bosco, Justine Schneider, Donna Maria Coleston-Shields, Lidia Sousa & Martin Orrell. (2019) Dyadic construction of dementia: meta-ethnography and behaviour-process synthesis. Aging & Mental Health 23:6, pages 651-659.
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Karen Hutchinson, Chris Roberts & Michele Daly. (2018) Identity, impairment and disablement: exploring the social processes impacting identity change in adults living with acquired neurological impairments. Disability & Society 33:2, pages 175-196.
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Aud Johannessen, Knut Engedal, Per Kristian Haugen, Marcia Cristina Nascimento Dourado & Kirsten Thorsen. (2018) “To be, or not to be”: experiencing deterioration among people with young-onset dementia living alone. International Journal of Qualitative Studies on Health and Well-being 13:1.
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Pat Sikes & Melanie Hall. (2017) ‘Every time I see him he’s the worst he’s ever been and the best he’ll ever be’: grief and sadness in children and young people who have a parent with dementia. Mortality 22:4, pages 324-338.
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Joany Millenaar, Lara Hvidsten, Marjolein E. de Vugt, Knut Engedal, Geir Selbæk, Torgeir Bruun Wyller, Aud Johannessen, Per Kristian Haugen, Christian Bakker, Deliane van Vliet, Raymond T.C.M. Koopmans, Frans R.J. Verhey & Hege Kersten. (2017) Determinants of quality of life in young onset dementia – results from a European multicenter assessment. Aging & Mental Health 21:1, pages 24-30.
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Elizabeth Kelson, Alison Phinney & Glen Lowry. (2017) Social citizenship, public art and dementia: Walking the urban waterfront with Paul’s Club. Cogent Arts & Humanities 4:1.
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Adriana Shnall, Adam Agate, Ana Grinberg, Maria Huijbregts, Minh-Quan Nguyen & Tiffany W. Chow. (2013) Development of supportive services for frontotemporal dementias through community engagement. International Review of Psychiatry 25:2, pages 246-252.
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M. Rebecca Genoe & SherryL. Dupuis. (2011) “I'm just like I always was”: a phenomenological exploration of leisure, identity and dementia. Leisure/Loisir 35:4, pages 423-452.
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Paula Jacobs, Karen Watchman, Heather Wilkinson & Louise Hoyle. (2023) Couples with intellectual disability where one partner has dementia – a scoping review exploring relationships in the context of dementia and intellectual disability. Ageing and Society, pages 1-40.
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Mary Pat Sullivan, Veronika Williams, Adetola Grillo, Roberta McKee-Jackson, Paul M Camic, Gill Windle, Joshua Stott, Emily Brotherhood & Sebastian J Crutch. (2022) Peer support for people living with rare or young onset dementia: An integrative review. Dementia 21:8, pages 2700-2726.
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Niamh Hennelly & Eamon O'Shea. (2021) A multiple perspective view of personhood in dementia. Ageing and Society 42:9, pages 2103-2121.
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Maziar Yazdanpanah. (2022) What's in a name? Address practices in Swedish residential care facilities. Journal of Aging Studies 61, pages 101007.
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Satomi Ikeuchi, Shizuko Omote, Koji Tanaka, Rie Okamoto, Yuko Morikawa & Osamu Iritani. (2020) Work‐related experiences of people living with young‐onset dementia in Japan. Health & Social Care in the Community 30:2, pages 548-557.
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Catherine V Talbot, Siobhan T O’Dwyer, Linda Clare & Janet Heaton. (2021) The use of Twitter by people with young-onset dementia: A qualitative analysis of narratives and identity formation in the age of social media. Dementia 20:7, pages 2542-2557.
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Cathal Blake & Louise Hopper. (2021) A qualitative investigation into family carers’ experiences of living with/caring for a person with young-onset dementia. International Journal of Care and Caring 5:3, pages 469-487.
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Fabiola Silvaggi, Matilde Leonardi, Pietro Tiraboschi, Cristina Muscio, Claudia Toppo & Alberto Raggi. (2020) Keeping People with Dementia or Mild Cognitive Impairment in Employment: A Literature Review on Its Determinants. International Journal of Environmental Research and Public Health 17:3, pages 842.
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Gullvi Flensner & Gudrun Rudolfsson. (2018) A pathway towards reconciliation and wellbeing. Nordisk sygeplejeforskning 8:2, pages 136-149.
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Nathália R. S. Kimura, Maria Alice T. Baptista, Raquel L. Santos, Maria da Gloria Portugal, Aud Johannenssen, Maria L. Barca, Knut Engedal, Jerson Laks, José Pedro Simões, Valeska Marinho Rodrigues & Marcia C. N. Dourado. (2018) Caregivers’ Perspectives of Quality of Life of People With Young- and Late-Onset Alzheimer Disease. Journal of Geriatric Psychiatry and Neurology 31:2, pages 76-83.
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Pat Sikes & Mel Hall. (2016) “It was then that I thought ‘whaat? This is not my Dad”: The implications of the ‘still the same person’ narrative for children and young people who have a parent with dementia. Dementia 17:2, pages 180-198.
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Emma Harding, Mary Pat Sullivan, Rachel Woodbridge, Keir X X Yong, Anne McIntyre, Mary L Gilhooly, Kenneth J Gilhooly & Sebastian J Crutch. (2018) ‘Because my brain isn’t as active as it should be, my eyes don’t always see’: a qualitative exploration of the stress process for those living with posterior cortical atrophy. BMJ Open 8:2, pages e018663.
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