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'Dignity and respect': An example of service user leadership and co-production in mental health research.

Faulkner A, Carr S, Gould D, Khisa C, Hafford-Letchfield T, Cohen R, Megele C, Holley J.
Health Expectations, doi: 10.1111/hex.12963. [Epub ahead of print]
Added: 23 January 2020

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'I thought it would be tiny little one phrase that we said, in a huge big pile of papers': children's reflections on their involvement in participatory research

Pinter A; Zandian S
Qualitative Research 15, 2, 235-250
Added: 19 September 2018

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‘I am not your nutter’: a personal reflection on commodification and comradeship in service user and survivor research.

Sarah Carr
Disability & Society, 34:7-8, 1140-1153.
Added: 12 December 2019

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‘I felt like a human being’—An exploratory, multi‐method study of refugee involvement in the development of mental health intervention research.

Georgina Warner, Zaruhi Baghdasaryan, Fatumo Osman, Elin Lampa, Anna Sarkadi.
Health Expectations, Epub ahead of print, DOI: 10.1111/hex.12990
Added: 19 December 2019

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‘Is it worth doing?’ Measuring the impact of patient and public involvement in research

Staley, K.
Research Involvement and Engagement, 1:6
Added: 14 October 2015

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‘Knowledge is power’: A framework for partnering with consumers in developing and delivering a scientific meeting in nephrology.

Emily Duncanson Kathryn Dansie Talia Gutman Allison Tong Martin Howell Shilpanjali Jesudason Donna Reidlinger Amber Williamson Nicole Scholes‐Robertson Lisa Murphy Carmel M Hawley Jonathan C Craig David W Johnson Stephen McDonald
Nephrology, Epub ahead of print, doi.org/10.1111/nep.13570
Added: 26 July 2019

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‘Patient Zero’: a critical investigation of the concept of public and patient involvement in the National Health Service

Macdonald S J; Taylor-Gooby D
Social Work and Social Sciences Review 17, 1, 5-21
Added: 19 September 2018

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‘We can make our research meaningful’ The impact of the Alzheimer’s Society Research Network.

Natasha Morgan, Anna Grinbergs-Saull and Matt Murray.
London: The Alzheimer's Society.
Added: 10 January 2019

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“About sixty per cent I want to do it”: Health researchers’ attitudes to, and experiences of, patient and public involvement (PPI)—A qualitative interview study.

Anne‐Marie Boylan , Louise Locock, Richard Thompson, Sophie Staniszewska.
Health Expectations Epub ahead of print doi.org/10.1111/hex.12883
Added: 27 April 2019

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“Getting to the Table”: Changing Ideas about Public and Patient Involvement in Canadian Drug Assessment.

Katherine Boothe
Journal of Health Politics, Policy and Law, 44 (4): 631-663.
Added: 12 December 2019

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