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Number of items: 20.

Sanderson, T., Hewlett, S., Calnan, M., Morris, M., Raza, K. and Kumar, K. (2012) Exploring the cultural validity of rheumatology outcomes. British Journal of Nursing, 21 (17). pp. 1015-1023. ISSN 0966-0461

Sanderson, T., Hewlett, S., Calnan, M. and Morris, M. (2012) Exploring the cultural validity of rheumatology outcomes. British Journal of Nursing, 21 (17). pp. 1015-1023. ISSN 0966-0461

Sanderson, T., Hewlett, S., Richards, P., Morris, M. and Calnan, M. (2012) Utilising qualitative data from nominal groups: Exploring the influences on treatment outcome prioritization with rheumatoid arthritis patients. Journal of Health Psychology , 17 (1). pp. 132-142. ISSN 1359-1053

Sanderson, T., Morris, M., Calnan, M., Richards, P. and Hewlett, S. (2011) Shifting normalities: Interactions of changing conceptions of a normal life and the normalisation of symptoms in rheumatoid arthritis. Sociology of Health and Illness, 33 (4). pp. 618-633. ISSN 1467-9566

Sanderson, T., Morris, M., Calnan, M., Richards, P. and Hewlett, S. (2010) Patient perspective of measuring treatment efficacy: The Rheumatoid Arthritis Patient Priorities for Pharmacological Interventions (RAPP-PI) outcomes. Arthritis Care & Research, 62 (5). pp. 647-656. ISSN 0004-3591

Sanderson, T., Morris, M., Calnan, M., Richards, P. and Hewlett, S. (2010) What outcomes from pharmacological treatments are important to people with rheumatoid arthritis? Creating the basis of a patient core set. Arthritis Care & Research, 62 (5). pp. 640-646. ISSN 0004-3591

Sanderson, T., Morris, M., Calnan, M., Richards, P. and Hewlett, S. (2010) ‘It’s this whole picture, this well-being’: patients’ understanding of ‘feeling well’ with rheumatoid arthritis. Chronic Illness, 6 (3). pp. 228-240. ISSN 1742-3953

Sanderson, T., Calnan, M., Morris, M., Richards, P. and Hewlett, S. (2009) The use of nominal groups to develop a patient-generated core set of treatment outcomes in rheumatoid arthritis. In: American College of Rheumatology, Philadelphia, USA, October 2009, Philadelphia, October 2009.

Sanderson, T., Calnan, M., Morris, M., Richards, P. and Hewlett, S. (2009) Well-being and normality in rheumatoid arthritis (RA): narratives of age, gender and ‘personhood’. In: Medical Sociology Group Annual Conference, Manchester, UK, 3-5 September 2009, Manchester, UK, 3-5 September, 2009.

Sanderson, T., Calnan, M., Morris, M., Richards, P. and Hewlett, S. (2009) The role of a patient research partner in a qualitative study about the meaning of well-being in rheumatoid arthritis. In: Medical Sociology Group Annual Conference, Manchester, UK, 3-5 September, 2009.

Sanderson, T., Calnan, M., Morris, M., Richards, P. and Hewlett, S. (2009) Using grounded theory with mixed methods: an example of a pragmatic study in rheumatology. In: Medical Sociology Conference, Liverpool, UK, 1 September 2009, Liverpool, UK, 1 September, 2009.

Sanderson, T., Calnan, M., Morris, M., Richards, P. and Hewlett, S. (2009) The impact of patient-perceived restricted access to anti-TNF therapy for rheumatoid arthritis: A qualitative study. Musculoskeletal Care, 7 (3). pp. 194-209. ISSN 1478-2189

Sanderson, T., Morris, M., Calnan, M., Richards, P. and Hewlett, S. (2009) Managing life with rheumatological conditions: Well-being. In: British Society for Rheumatology Conference, Liverpool, UK, April 2009, Liverpool, UK, April 2009. Liverpool, UK: UNSPECIFIED

Sanderson, T., Calnan, M., Morris, M., Richards, P. and Hewlett, S. (2009) The impact of restricted access to anti-TNF therapy on people with rheumatoid arthritis: A qualitative study. Musculoskeletal Care, 7 (3). pp. 194-209. ISSN 1478-2189

Sanderson, T., Morris, M., Calnan, M., Richards, P. and Hewlett, S. (2008) Developing a patient-generated core set of treatment outcomes in rheumatoid arthritis (RA): Using nominal groups with patients to prioritise outcomes of pharmacological interventions. In: American College of Rheumatology Conference, San Fransisco, USA, October 2008, San Fransisco, USA, October 2008.

Sanderson, T., Calnan, M., Morris, M., Richards, P. and Hewlett, S. (2008) Defining well-being in rheumatoid arthritis: Potential outcomes for a patient generated core set. In: British Rheumatology Society Conference, Liverpool, UK, 22-25 April, 2008, Liverpool, UK, 22 - 25 April 2008.

Sanderson, T., Calnan, M., Morris, M., Richards, P. and Hewlett, S. (2008) Positive experiences of living with rheumatoid arthritis: Social and personal growth link to adaptation. In: British Rheumatology Society Conference, Liverpool, UK, 22-25 April, 2008, Liverpool, UK, 22 - 25 April 2008.

Sanderson, T., Calnan, M., Morris, M., Richards, P. and Hewlett, S. (2008) The role of identity in well-being and normality on rheumatoid arthritis: Narratives of age, gender and 'personhood'. In: British Rheumatology Society Conference, Liverpool, UK, 22-25 April 2008, Liverpool, UK, 22 - 25 April 2008.

Sanderson, T., Calnan, M., Morris, M., Richards, P. and Hewlett, S. (2008) Measuring well-being in rheumatoid arthritis (RA): The development of five well-being numerical rating scales (NRS). In: British Society of Rheumatology, Glasgow, Scotland, April, 2008.

Sanderson, T., Calnan, M., Morris, M., Richards, P. and Hewlett, S. (2008) Rheumatoid arthritis patients’ interpretation of the DAS patient global used at Bristol Royal Infirmary. In: British Society of Rheumatology Conference, Glasgow, Scotland, April 2008, Glasgow, Scotland, April, 2008.

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