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

Key health outcomes for children and young people with neurodisability: qualitative research with young people and parents

(2014) Amanda Allard et al.   BMJ Open

Study protocol: longitudinal study of the transition of young people with complex health needs from child to adult health services

(2013) Allan F Colver et al.   BMC PUBLIC HEALTH

Towards a definition of neurodisability: a Delphi survey

(2013) Christopher Morris et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Mapping the impact of patient and public involvement on health and social care research: a systematic review

(2012) Jo Brett et al.   HEALTH EXPECTATIONS

Research Priorities for Developmental-Behavioral Pediatrics

(2012) Nathan J. Blum et al.   JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS

Changes Over Time in the Health of Caregivers of Children With Health Problems: Growth-Curve Findings From a 10-Year Canadian Population-Based Study

(2011) Jamie C. Brehaut et al.   AMERICAN JOURNAL OF PUBLIC HEALTH

Why it is crucial to involve families in all stages of childhood disability research

(2011) Christopher Morris et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Which Neurodevelopmental Disorders Get Researched and Why?

(2010) Dorothy V. M. Bishop   PLoS One

Consensus research priorities for cerebral palsy: a Delphi survey of consumers, researchers, and clinicians

(2009) SARAH MCINTYRE et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Avoidable waste in the production and reporting of research evidence

(2009) Iain Chalmers et al.   LANCET