Psychosocial Factors That Shape Patient and Carer Experiences of Dementia Diagnosis and Treatment: A Systematic Review of Qualitative Studies
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Title
Psychosocial Factors That Shape Patient and Carer Experiences of Dementia Diagnosis and Treatment: A Systematic Review of Qualitative Studies
Authors
Keywords
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Journal
PLOS MEDICINE
Volume 9, Issue 10, Pages e1001331
Publisher
Public Library of Science (PLoS)
Online
2012-10-31
DOI
10.1371/journal.pmed.1001331
References
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- Process of ambivalent normalisation: experience of family caregivers of elders with mild cognitive impairment in Taiwan
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- Experience and Perspectives of Caregivers of Spouse with Mild Cognitive Impairment
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- Appropriate disclosure of a diagnosis of dementia: identifying the key behaviours of 'best practice'
- (2008) Jan Lecouturier et al. BMC HEALTH SERVICES RESEARCH
- Methods for the thematic synthesis of qualitative research in systematic reviews
- (2008) James Thomas et al. BMC Medical Research Methodology
- Attitudes and support needs of Black Caribbean, south Asian and White British carers of people with dementia in the UK
- (2008) Vanessa Lawrence et al. BRITISH JOURNAL OF PSYCHIATRY
- Narratives in a users' and carers' group: meanings and impact
- (2008) Susan M. Benbow et al. INTERNATIONAL PSYCHOGERIATRICS
- How do elderly spouse care givers of people with Alzheimer disease experience the disclosure of dementia diagnosis and subsequent care?
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- Resisting social disenfranchisement: Negotiating collective identities and everyday life with memory loss
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- Mild cognitive impairment: coping with an uncertain label
- (2007) Liesbeth Joosten-Weyn Banningh et al. INTERNATIONAL JOURNAL OF GERIATRIC PSYCHIATRY
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