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Number of items: 3.

Tillett, W., Adebajo, A., Brooke, M., Campbell, W., Coates, L. C., FitzGerald, O., Gossec, L., Helliwell, P., Hewlett, S., James, J., Minnock, P., Reast, A., O’Sullivan, D., de Wit, M. and McHugh, N. (2014) Patient involvement in outcome measures for psoriatic arthritis. Current Rheumatology Reports, 16 (5). p. 418. ISSN 1523-3774 Available from:

Staniszewska, S., Adebajo, A., Barber, R., Beressford, P., Brady, L.-M., Brett, J., Elliott, J., Evans, D., Haywood, K., Jones, D., Mockford, C., Nettle, M., Rose, D. and Williamson, T. (2011) Developing the evidence base of patient and public involvement in health and social care research: The case for measuring impact. International Journal of Consumer Studies, 35 (6). pp. 628-632. ISSN 1470-6243 Available from:

Kirwan, J. R., Minnock, P., Adebajo, A., Bresnihan, B., Choy, E., De Wit, M., Hazes, M., Richards, P., Saag, K., Suarez-Almazor, M., Wells, G. and Hewlett, S. (2007) Patient perspective workshop: Fatigue as a recommended patient-centred outcome measure in rheumatoid arthritis. Journal of Rheumatology, 34 (5). pp. 1174-1177. ISSN 0315-162X Available from:

This list was generated on Tue Dec 1 04:00:22 2015 GMT.


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