Quality of Life
2009
Rosenbaum P (2009). Commentary: A randomized controlled trial of the impact of therapeutic horse riding on the quality of life, health, and function of children with cerebral palsy. Developmental Medicine & Child Neurology, 51:88-91.
2008
Janssens L, Gorter JW, Ketelaar M, Kramer WLM, Holtslag H (2008). Health-related quality-of-life measures for long-term follow-up in children after major trauma. Quality of Life Research, 17(5):701-13.
Klassen A, Klaassen R, Dix D, Pritchard S, O'Donnell M, Scott A, Sung L (2008). Impact of caring for a child with cancer on parents' quality of life. Journal of Clinical Oncology, 26(36):5884-5889.
Livingston MH, Rosenbaum PL (2008). Adolescents with cerebral palsy: stability in quality of life and health-related quality of life over one year. Developmental Medicine and Child Neurology, 50(9):696-701.
Majnemer A, Shevell M, Law M, Poulin C, Rosenbaum P (2008). Reliability in the ratings of quality of life between parents and their children of school age with cerebral palsy. Quality of Life Research, 17(9):1163-71.
2007
Livingston, M. H., Rosenbaum, P. L., Russell, D. J., & Palisano, R. J. (2007). Quality of life among adolescents with cerebral palsy: What does the literature tell us? Developmental Medicine & Child Neurology, 49(3), 225-231.
Majnemer, A., Shevell, M., Rosenbaum, P., Law, M., & Poulin, C. (2007). Determinants of life quality in school-age children with cerebral palsy. Journal of Pediatrics, 151(5), 470-5, 475.e1-3.
Rosenbaum, P. L., Livingston, M. H., Palisano, R. J., Galuppi, B. E., & Russell, D. J. (2007). Quality of life and health-related quality of life of adolescents with cerebral palsy. Developmental Medicine & Child Neurology, 49(7), 516-521.
2006
King, G. A., Zwaigenbaum, L., King, S., Baxter, D., Rosenbaum, P., & Bates, A. (2006). A qualitative investigation of changes in the belief systems of families of children with autism or down syndrome. Child: Care, Health and Development, 32(3), 353-369.
Klassen, A. F., Miller, A., & Fine, S. (2006). Agreement between parent and child report of quality of life in children with attention-deficit/hyperactivity disorder. Child: Care, Health & Development, 32(4), 397-406.
Lach, L. M., Ronen, G. M., Rosenbaum, P. L., Cunningham, C., Boyle, M. H., Bowman, S., et al. (2006). Health-related quality of life in youth with epilepsy: Theoretical model for clinicians and researchers. part I: The role of epilepsy and co-morbidity. Quality of Life Research, 15(7), 1161-1171.
2004
A qualitative study of the transition to adulthood for youth with physical disabilities
Frequency and determinants of formal respite service use among caregivers of children with cerebral palsy
The health of primary caregivers of children with cerebral palsy: How does it compare with that of other Canadian caregivers?
The World Health Organization International Classification of Functioning, Disability, and Health: a model to guide clinical thinking, practice and research in cerebral palsy
2001
A qualitative study of the transition to adulthood for youth with physical disabilities
2000
Quality of life in Spina Bifida: Importance of parental hope
Success in life for older adolescents with cerebral palsy
The self-esteem of adolescents with mental health problems: Theory meets practice
1999
Family-centered caregiving and well-being of parents of children with disabilities: Linking process with outcome
Health-related quality of life in childhood epilepsy: Children's participation in identifying the components
Health-related quality of life in childhood epilepsy: Children's participation in identifying the components
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