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
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The role of information system in multiple sclerosis managementMultiple sclerosis: clinical profiling and data collection as prerequisite for personalized medicine approachUnderstanding Drivers of Employment Changes in a Multiple Sclerosis Population.A case study of the Secure Anonymous Information Linkage (SAIL) Gateway: a privacy-protecting remote access system for health-related research and evaluation.Physical disability, anxiety and depression in people with MS: an internet-based survey via the UK MS Register.A large-scale study of anxiety and depression in people with Multiple Sclerosis: a survey via the web portal of the UK MS Register.Infodemiology and infoveillance of multiple sclerosis in ItalyThe physical and psychological impact of multiple sclerosis using the MSIS-29 via the web portal of the UK MS Register.How people with multiple sclerosis rate their quality of life: an EQ-5D survey via the UK MS register.Tablet-based screening improves continence management in multiple sclerosisSunshine, Sea, and Season of Birth: MS Incidence in WalesDesigning an Electronic Patient Management System for Multiple Sclerosis: Building a Next Generation Multiple Sclerosis Documentation System.Squinting through layers of fog: assessing the cost effectiveness of treatments for multiple sclerosis.Supporting work for people with multiple sclerosis.A Qualitative Study of the Barriers and Opportunities for Adoption of Web-Portals for Doctors and Patients in Russia.Multiple sclerosis: relapses, resource use, and costs.Measuring the quality of life in patients with multiple sclerosis in clinical practice: a necessary challenge.Access to and Use of Clinical Services and Disease-Modifying Therapies by People with Progressive Multiple Sclerosis in the United Kingdom.The Swiss Multiple Sclerosis Registry (SMSR): study protocol of a participatory, nationwide registry to promote epidemiological and patient-centered MS research
P2860
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P2860
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
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2012 nî lūn-bûn
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2012 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2012年の論文
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2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
The feasibility of collecting ...... ing a cohort of people with MS
@ast
The feasibility of collecting ...... ing a cohort of people with MS
@en
The feasibility of collecting ...... ing a cohort of people with MS
@nl
type
label
The feasibility of collecting ...... ing a cohort of people with MS
@ast
The feasibility of collecting ...... ing a cohort of people with MS
@en
The feasibility of collecting ...... ing a cohort of people with MS
@nl
prefLabel
The feasibility of collecting ...... ing a cohort of people with MS
@ast
The feasibility of collecting ...... ing a cohort of people with MS
@en
The feasibility of collecting ...... ing a cohort of people with MS
@nl
P2093
P2860
P50
P3181
P356
P1476
The feasibility of collecting ...... ing a cohort of people with MS
@en
P2093
Hazel Lockhart-Jones
Inocencio Dc Maramba
Lisa A Osborne
P2860
P2888
P3181
P356
10.1186/1472-6947-12-73
P407
P577
2012-07-18T00:00:00Z
P5875
P6179
1038156141