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Seminars in Neonatology : SN|June 22, 2000
Measurement of health status and quality of life in neonatal follow-up studiesA Colver, C JessenChild: Care, Health and Development|November 18, 2003
A qualitative study, using focused interviews, of the information needs of families whose children's names are on a cerebral palsy registerJ Miller, J Colligan, A ColverChild: Care, Health and Development|January 30, 2018
Are the health needs of young people with cerebral palsy met during transition from child to adult health care?F Solanke, A Colver, H McConachie, et al.Public Health|December 13, 2005
How might districts identify local barriers to participation for children with cerebral palsy?B Welsh, S Jarvis, D Hammal, et al.BMJ (Clinical Research Ed.)|April 30, 1994
Do interventions that improve immunisation uptake also reduce social inequalities in uptake?R Reading, A Colver, S Openshaw, et al.Archives of Disease in Childhood|February 12, 2009
Psychological problems in children with hemiplegia: a European multicentre surveyJ Parkes, M White-Koning, N McCullough, et al.Pediatric Rehabilitation|October 20, 2006
A qualitative study of the physical, social and attitudinal environments influencing the participation of children with cerebral palsy in northeast EnglandK Lawlor, S Mihaylov, B Welsh, et al.Archives of Disease in Childhood|May 6, 2008
Dasl(n)e: the challenge of developing a regional database for autism spectrum disorderH McConachie, R Barry, A Spencer, et al.Eye (London, England)|January 1, 1996
Preschool vision screening: a prospective comparative evaluationL C Bray, M P Clarke, S N Jarvis, et al.Child: Care, Health and Development|January 31, 2006
Discussion groups with parents of children with cerebral palsy in Europe designed to assist development of a relevant measure of environmentV McManus, S I Michelsen, K Parkinson, et al.Pageof 2