Cerebral Palsy and Special Needs Children's Organization. Help Support and Information About Cerebral Palsy - 4MyChild. 4MyChild:Help and Hope For Life. Retrieved April 24, 2011, from http://www.cerebralpalsy.org/
Chen, Y., Kang, L., Chuang, T., Doong, J., Lee, S., Tsai, M., Jeng, S., & Sung, W. (2007). Use of Virtual Reality to Improve Upper-Extremity Control in Children With Cerebral Palsy: A Single-Subject Design. Physical Therapy, 87(11), 1441-57. Retrieved April 25, 2011, from Health Module. (Document ID: 1378290751).
Davis, E., Shelly, A., Waters, E., Boyd, R., Cook, K. and Davern, M. (2010), The impact of caring for a child with cerebral palsy: quality of life for mothers and fathers. Child: Care, Health and Development, 36: 63–73. doi: 10.1111/j.1365-2214.2009.00989.x
Griffin, H.C., Fitch, K.L., Griffin, L.W. (2002). Causes and interventions in the area of cerebral palsy. Infants & Young Children, 14(3), Retrieved from http://ovidsp.tx.ovid.com.proxy.library.vanderbilt.edu
Hayn, J., Hazlett, L., & Sweeney, W.. (2009, April). Facilitating Inclusion: Young Adult Literature as a Tool. English Leadership Quarterly, 31(4), 8-11. Retrieved April 25, 2011, from ProQuest Education Journals. (Document ID: 1686976371).
Huang, I.-C., Sugden, D. and Beveridge, S. (2009), Assistive devices and cerebral palsy: factors influencing the use of assistive devices at home by children with cerebral palsy. Child: Care, Health and Development, 35: 130–139. doi: 10.1111/j.1365-2214.2008.00898.x
Nemours Network, The. (2011). Cerebral Palsy. Kids Health. Retrieved April, 24 2011, from http://kidshealth.org/parent/medical/brain/cerebral_palsy.html#
Palisano, R. J., Almarsi, N., Chiarello, L. A., Orlin, M. N., Bagley, A. and Maggs, J. (2010), Family needs of parents of children and youth with cerebral palsy. Child: Care, Health and Development, 36: 85–92. doi: 10.1111/j.1365-2214.2009.01030.x
Reading, R. (2009), Effectiveness of physical therapy interventions for children with cerebral palsy: a systematic review. Child: Care, Health and Development, 35: 140–141. doi: 10.1111/j.1365-2214.2008.00921_2.x
Shikako-Thomas, K., Lach, L., Majnemer, A., Nimigon, J., Cameron , K. & Shevell, M. (2009). Quality of life from the perspective of adolescents with cerebral palsy: ‘‘i just think i’m a normal kid, i just happen to have a disability". Quality of Life Research, 18. Retrieved from http://www.springerlink.com.proxy.library.vanderbilt.edu/content/l7481kw4um12q612/fulltext.pdf doi: DOI 10.1007/s11136-009-9501-3
Sipal, R. F., Schuengel, C., Voorman, J. M., Van Eck, M. and Becher, J. G. (2010), Course of behaviour problems of children with cerebral palsy: the role of parental stress and support. Child: Care, Health and Development, 36: 74–84. doi: 10.1111/j.1365-2214.2009.01004.x
Treatments for cerebral palsy: making choices of intervention from an expanding menu of options. (1998). Infants & Young Children, 10(4), Retrieved from http://ovidsp.tx.ovid.com.proxy.library.vanderbilt.edu
Vogts, N., Mackey, A. H., Ameratunga, S. and Stott, N. S. (2010), Parent-perceived barriers to participation in children and adolescents with cerebral palsy. Journal of Paediatrics and Child Health, 46: 680–685. doi: 10.1111/j.1440-1754.2010.01815.x
Waters, E., Maher, E., Salmon, L., Reddihough, D. and Boyd, R. (2005), Development of a condition-specific measure of quality of life for children with cerebral palsy: empirical thematic data reported by parents and children. Child: Care, Health and Development, 31: 127–135. doi: 10.1111/j.1365-2214.2004.00476.x
Next: Additional Resources
