Cargando…
Personal and societal costs of multiple sclerosis in the UK: A population-based MS Registry study
OBJECTIVES: To investigate through survey and data linkage, healthcare resource use and costs (except drugs), including who bears the cost, of multiple sclerosis in the United Kingdom by disease severity and type. METHODS: The United Kingdom Multiple Sclerosis Register deployed a cost of illness sur...
Autores principales: | Nicholas, Richard S, Heaven, Martin L, Middleton, Rodden M, Chevli, Manoj, Pulikottil-Jacob, Ruth, Jones, Kerina H, Ford, David V |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977221/ https://www.ncbi.nlm.nih.gov/pubmed/32030197 http://dx.doi.org/10.1177/2055217320901727 |
Ejemplares similares
-
The Physical and Psychological Impact of Multiple Sclerosis Using the MSIS-29 via the Web Portal of the UK MS Register
por: Jones, Kerina H., et al.
Publicado: (2013) -
How People with Multiple Sclerosis Rate Their Quality of Life: An EQ-5D Survey via the UK MS Register
por: Jones, Kerina H., et al.
Publicado: (2013) -
A Large-Scale Study of Anxiety and Depression in People with Multiple Sclerosis: A Survey via the Web Portal of the UK MS Register
por: Jones, Kerina H., et al.
Publicado: (2012) -
Physical Disability, Anxiety and Depression in People with MS: An Internet-Based Survey via the UK MS Register
por: Jones, Kerina H., et al.
Publicado: (2014) -
The feasibility of collecting information from people with Multiple Sclerosis for the UK MS Register via a web portal: characterising a cohort of people with MS
por: Ford, David V, et al.
Publicado: (2012)