Valuing biomarker diagnostics for dementia care: enhancing the reflection of patients, their care-givers and members of the wider public
Author:
Funder
ZonMW
Publisher
Springer Science and Business Media LLC
Subject
Health Policy,Education,Health (social science)
Link
http://link.springer.com/article/10.1007/s11019-018-09883-2/fulltext.html
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3. Boote, J., R. Barber, and C. Cooper. 2006. Principles and indicators of successful consumer involvement in NHS research: Results of a Delphi study and subgroup analysis. Health Policy 75 (3): 280–297.
4. Bunn, F., C. Goodman, K. Sworn, G. Rait, C. Brayne, L. Robinson, E. McNeilly, and S. Iliffe. 2012. Psychosocial factors that shape patient and carer experiences of dementia diagnosis and treatment: A systematic review of qualitative studies. PLoS Medicine. https://doi.org/10.1371/journal.pmed.1001331 .
5. Burget, M., E. Bardone, and M. Pedaste. 2016. Definitions and conceptual dimensions of responsible research and innovation: A literature review. Science and Engineering Ethics 23 (1): 1–19.
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3. Ambivalent anticipation: How people with Alzheimer’s disease value diagnosis in current and envisioned future practices;Sociology of Health & Illness;2021-02
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