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Clinical Orthopaedics and Related Research|May 12, 2010
The potential research impact of patient reported outcomes on osteogenesis imperfectaCatherine A Brownstein, Paul Wicks
Movement Disorders : Official Journal of the Movement Disorder Society|April 9, 2009
Pathological gambling amongst Parkinson's disease and ALS patients in an online community (PatientsLikeMe.com)Paul Wicks, Graeme J A MacPhee
The Patient|November 7, 2013
Quality of life in organ transplant recipients participating in an online transplant communityPaul Wicks, Katherine A Sulham, Ari Gnanasakthy
Journal of Medical Internet Research|January 27, 2011
Use of an online community to develop patient-reported outcome instruments: the Multiple Sclerosis Treatment Adherence Questionnaire (MS-TAQ)Paul Wicks, Michael Massagli, Amit Kulkarni, et al.
Health and Quality of Life Outcomes|June 20, 2012
The multiple sclerosis rating scale, revised (MSRS-R): development, refinement, and psychometric validation using an online communityPaul Wicks, Timothy E Vaughan, Michael P Massagli
Research Involvement and Engagement|March 7, 2018
Patients' motivations and interest in research: characteristics of volunteers for patient-led projects on PatientsLikeMeMeaghan Bradley, Julia Braverman, Magdalena Harrington, et al.
Journal of Pharmaceutical Policy and Practice|November 2, 2016
Medicine and the future of health: reflecting on the past to forge aheadDale Fisher, Paul Wicks, Zaheer-Ud-Din Babar
Journal of Medical Internet Research|January 25, 2013
Quantifying short-term dynamics of Parkinson's disease using self-reported symptom data from an Internet social networkMax Little, Paul Wicks, Timothy Vaughan, et al.
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