Glaser A, Stahmann A, Meissner T, et al. Multiple sclerosis registries in Europe – an updated mapping survey. Multiple Sclerosis and Related Disorders [online serial]. Epub 2018 Oct. Accessed at: https://linkinghub.elsevier.com/retrieve/pii/S2211034818303614.
Middleton R, Rodgers W, Chataway J, et al. Validating the Portal Population of the United Kingdom Multiple Sclerosis Register. Multiple Sclerosis and Related Disorders [online serial]. Epub 2018 May. Accessed at: http://linkinghub.elsevier.com/retrieve/pii/S2211034818301767.
Balbuena LD, Middleton RM, Tuite-Dalton K, Pouliou T, Williams KE, Noble GJ. Sunshine, Sea, and Season of Birth: MS Incidence in Wales. Burne THJ, editor. PLOS ONE. 2016;11:e0155181.
Osborne LA, Gareth Noble J, Maramba IDC, et al. Outcome measures for multiple sclerosis. Physical Therapy Reviews. 2014;19:24–38.
Jones KH, Jones PA, Middleton RM, et al. Physical Disability, Anxiety and Depression in People with MS: An Internet-Based Survey via the UK MS Register. Reindl M, editor. PLoS ONE. 2014;9:e104604.
Osborne LA, Middleton RM, Jones KH, Ford DV, Noble JG. Desirability and expectations of the UK MS Register: Views of people with MS. International Journal of Medical Informatics. 2013;82:1104–1110.
Jones KH, Ford DV, Jones PA, et al. How People with Multiple Sclerosis Rate Their Quality of Life: An EQ-5D Survey via the UK MS Register. Reindl M, editor. PLoS ONE. 2013;8:e65640.
Osborne LA, Lockhart-Jones HM, Middleton RM, et al. Identifying and Addressing the Barriers to the Use of an Internet-Register for Multiple Sclerosis: International Journal of Healthcare Information Systems and Informatics. 2013;8:1–16.
Jones KH, Ford DV, Jones PA, et al. The Physical and Psychological Impact of Multiple Sclerosis Using the MSIS-29 via the Web Portal of the UK MS Register. Reindl M, editor. PLoS ONE. 2013;8:e55422.