Citations (22)
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Vivien P. Nichols, Esther Williamson, Francine Toye & Sarah E. Lamb. (2017) A longitudinal, qualitative study exploring sustained adherence to a hand exercise programme for rheumatoid arthritis evaluated in the SARAH trial. Disability and Rehabilitation 39:18, pages 1856-1863.
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Articles from other publishers (21)
Su-Hui Chen, Kuang-Hui YuDr.Dr., Yi-Chun Kao & Jung-Hua Shao. (2021) It Is Like a Puppet Show-Experiences of Rheumatoid Arthritis Among Adult Chinese: A Qualitative Study. Clinical Nursing Research 31:5, pages 795-802.
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Javier Martinez-Calderon, Javier Matias-Soto & Alejandro Luque-Suarez. (2022) “My Pain Is Unbearable…I Cannot Recognize Myself!” Emotions, Cognitions, and Behaviors of People Living With Musculoskeletal Disorders: An Umbrella Review. Journal of Orthopaedic & Sports Physical Therapy 52:5, pages 243-A102.
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Clara Mukuria, Janice Connell, Jill Carlton, Tessa Peasgood, Alison Scope, Mark Clowes, Stacey Rand, Karen Jones & John Brazier. (2022) Qualitative Review on Domains of Quality of Life Important for Patients, Social Care Users, and Informal Carers to Inform the Development of the EQ-HWB. Value in Health 25:4, pages 492-511.
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Krushna Chandra Sahoo. 2022. Rheumatoid Arthritis. Rheumatoid Arthritis.
Colleen Johnston-Devin, Florin Oprescu, Marion Gray & Marianne Wallis. (2021) Patients Describe their Lived Experiences of Battling to Live with Complex Regional Pain Syndrome. The Journal of Pain 22:9, pages 1111-1128.
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Susie Donnelly, Anthony G. Wilson, Hasheem Mannan, Claire Dix, Laura Whitehill & Thilo Kroll. (2021) (In)Visible illness: A photovoice study of the lived experience of self-managing rheumatoid arthritis. PLOS ONE 16:3, pages e0248151.
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Evi Germeni, Ruth Garside, Julia Frost, Morwenna Rogers & Nicky Britten. (2021) Can a Meta-ethnography Be Updated by Different Reviewers? Reflections From a Recent Update. International Journal of Qualitative Methods 20, pages 160940692110464.
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Francine Toye & Karen L. Barker. (2020) A meta-ethnography to understand the experience of living with urinary incontinence: ‘is it just part and parcel of life?’. BMC Urology 20:1.
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Susie Donnelly, Molly Manning, Hasheem Mannan, Anthony G. Wilson & Thilo Kroll. (2020) Renegotiating dimensions of the self: A systematic review and qualitative evidence synthesis of the lived experience of self‐managing rheumatoid arthritis. Health Expectations 23:6, pages 1388-1411.
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Avinash Jain, Amita Aggarwal, Jo Adams, Rachel E. Jordan, Steven Sadhra, Shirish Dubey, Kerry Allen & Kanta Kumar. (2020) Delay in seeking medical help in patients with rheumatoid arthritis in India: A qualitative study. International Journal of Rheumatic Diseases 23:12, pages 1707-1718.
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Giulia Parenti, Silvia Caterina Maria Tomaino & Sabrina Cipolletta. (2020) The experience of living with rheumatoid arthritis: A qualitative metasynthesis. Journal of Clinical Nursing 29:21-22, pages 3922-3936.
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Fran Toye, Kate Seers & Karen Louise Barker. (2019) Living life precariously with rheumatoid arthritis - a mega-ethnography of nine qualitative evidence syntheses. BMC Rheumatology 3:1.
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Evi Germeni, Julia Frost, Ruth Garside, Morwenna Rogers, Jose M Valderas & Nicky Britten. (2018) Antibiotic prescribing for acute respiratory tract infections in primary care: an updated and expanded meta-ethnography. British Journal of General Practice 68:674, pages e633-e645.
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G. Colligan, J. Galloway & H. Lempp. (2017) Recipients’ and providers’ perspectives of obesity and potential barriers to weight management programmes in patients with Rheumatoid Arthritis (RA): a qualitative study. BMC Obesity 4:1.
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Sidona-Valentina Bala, Karin Samuelson, Peter Hagell, Bengt Fridlund, Kristina Forslind, Björn Svensson & Bibbi Thomé. (2017) Living with persistent rheumatoid arthritis: a BARFOT study. Journal of Clinical Nursing 26:17-18, pages 2646-2656.
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Emma F. France, Mary Wells, Heidi Lang & Brian Williams. (2016) Why, when and how to update a meta-ethnography qualitative synthesis. Systematic Reviews 5:1.
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Mohammed A. Mohammed, Rebekah J. Moles & Timothy F. Chen. (2016) Meta-synthesis of qualitative research: the challenges and opportunities. International Journal of Clinical Pharmacy.
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Colleen M. Johnston, Florin I. Oprescu & Marion Gray. (2015) Building the evidence for CRPS research from a lived experience perspective. Scandinavian Journal of Pain 9:1, pages 30-37.
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Gavin Daker-White, Rebecca Hays, Jennifer McSharry, Sally Giles, Sudeh Cheraghi-Sohi, Penny Rhodes & Caroline Sanders. (2015) Blame the Patient, Blame the Doctor or Blame the System? A Meta-Synthesis of Qualitative Studies of Patient Safety in Primary Care. PLOS ONE 10:8, pages e0128329.
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Francis Berenbaum, Pierre Chauvin, Christophe Hudry, Florence Mathoret-Philibert, Maud Poussiere, Thibault De Chalus, Caroline Dreuillet, Françoise Russo-Marie, Jean-Michel Joubert & Alain Saraux. (2014) Fears and Beliefs in Rheumatoid Arthritis and Spondyloarthritis: A Qualitative Study. PLoS ONE 9:12, pages e114350.
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Gavin Daker-White, John Ealing, Julie Greenfield, Helen Kingston, Caroline Sanders & Katherine Payne. (2013) Trouble with ataxia: A longitudinal qualitative study of the diagnosis and medical management of a group of rare, progressive neurological conditions. SAGE Open Medicine 1, pages 205031211350556.
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