Browsing Institute of Health Research by Author "Allard, A"
Now showing items 1-4 of 4
Issue Date | Title | Author(s) |
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1 May 2014 | Informing the NHS Outcomes Framework: evaluating meaningful health outcomes for children with neurodisability using multiple methods including systematic review, qualitative research, Delphi survey and consensus meeting. | Morris, C; Janssens, A; Allard, A; et al. |
19 April 2014 | Key health outcomes for children and young people with neurodisability: qualitative research with young people and parents. | Allard, A; Fellowes, A; Shilling, V; et al. |
25 June 2015 | Meaningful health outcomes for paediatric neurodisability: stakeholder prioritisation and appropriateness of patient reported outcome measures | Morris, C; Janssens, A; Shilling, V; et al. |
2015 | Setting research priorities to improve the health of children and young people with neurodisability: a British Academy of Childhood Disability-James Lind Alliance Research Priority Setting Partnership. | Morris, C; Simkiss, D; Busk, M; et al. |