Dr Paula Bray

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Current research students

Project title Research student
Powered wheelchair standing devices - impact on the quality of life, participation and the clinical course of Duchenne Muscular Dystrophy - a pilot study in NSW. Helena YOUNG

Selected publications

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Book Chapters

  • Bray, P., Burns, J., Morrison, M., Bundy, A. (2010). Measuring Health-Related Quality of Life in Children with Neuromuscular Disorders. In Columbus, A.M. (Eds.), Advances in Psychology Research, Vol. 65, (pp. 177-190). New York: Nova Science Publishers.

Journals

  • Bray, P., Bundy, A., Ryan, M., North, K. (2017). Can in-the-moment diary methods measure health-related quality of life in Duchenne muscular dystrophy? Quality of Life Research, 26(5), 1145-1152. [More Information]
  • Kunovsky, D., Cordier, R., Bray, P., Burns, J. (2017). Handwriting difficulties of children with Charcot-Marie-Tooth disease type 1A. Journal of the Peripheral Nervous System, 22(1), 34-38. [More Information]
  • Bundy, A., Kolrosova, J., Paguinto, S., Bray, P., Swain, B., Wallen, M., Engelen, L. (2011). Comparing the Effectiveness of a Parent Group Intervention with Child-Based Intervention for Promoting Playfulness in Children with Disabilities. Israeli Journal of Occupational Therapy, 20(4), 95-114.
  • Bray, P., Bundy, A., Ryan, M., North, K., Burns, J. (2011). Health status of boys with Duchenne muscular dystrophy: A parent's perspective. Journal of Paediatrics and Child Health, 47, 557-562. [More Information]
  • Bray, P., Bundy, A., Ryan, M., North, K. (2010). Feasibility of a computerized method to measure quality of "everyday" life in children with neuromuscular disorders. Physical and Occupational Therapy in Pediatrics, 30(1), 43-53. [More Information]
  • Bray, P., Bundy, A., Ryan, M., North, K., Everett, A. (2010). Health-related Quality of Life in Boys With Duchenne Muscular Dystrophy: Agreement Between Parents and Their Sons. Journal of Child Neurology, 25(10), 1188-1194. [More Information]
  • Burns, J., Bray, P., Cross, L., North, K., Ouvrier, R., Ryan, M. (2008). Hand involvement in children with Charcot-Marie-Tooth disease type 1A. Neuromuscular Disorders, 18(12), 970-973. [More Information]

Conferences

  • Bray, P., Bundy, A. (2006). Experience sampling methodology in children with neuromuscular disorders: A feasibility study. Fifth Research Conference 2006. University of Sydney.

2017

  • Bray, P., Bundy, A., Ryan, M., North, K. (2017). Can in-the-moment diary methods measure health-related quality of life in Duchenne muscular dystrophy? Quality of Life Research, 26(5), 1145-1152. [More Information]
  • Kunovsky, D., Cordier, R., Bray, P., Burns, J. (2017). Handwriting difficulties of children with Charcot-Marie-Tooth disease type 1A. Journal of the Peripheral Nervous System, 22(1), 34-38. [More Information]

2011

  • Bundy, A., Kolrosova, J., Paguinto, S., Bray, P., Swain, B., Wallen, M., Engelen, L. (2011). Comparing the Effectiveness of a Parent Group Intervention with Child-Based Intervention for Promoting Playfulness in Children with Disabilities. Israeli Journal of Occupational Therapy, 20(4), 95-114.
  • Bray, P., Bundy, A., Ryan, M., North, K., Burns, J. (2011). Health status of boys with Duchenne muscular dystrophy: A parent's perspective. Journal of Paediatrics and Child Health, 47, 557-562. [More Information]

2010

  • Bray, P., Bundy, A., Ryan, M., North, K. (2010). Feasibility of a computerized method to measure quality of "everyday" life in children with neuromuscular disorders. Physical and Occupational Therapy in Pediatrics, 30(1), 43-53. [More Information]
  • Bray, P., Bundy, A., Ryan, M., North, K., Everett, A. (2010). Health-related Quality of Life in Boys With Duchenne Muscular Dystrophy: Agreement Between Parents and Their Sons. Journal of Child Neurology, 25(10), 1188-1194. [More Information]
  • Bray, P., Burns, J., Morrison, M., Bundy, A. (2010). Measuring Health-Related Quality of Life in Children with Neuromuscular Disorders. In Columbus, A.M. (Eds.), Advances in Psychology Research, Vol. 65, (pp. 177-190). New York: Nova Science Publishers.

2008

  • Burns, J., Bray, P., Cross, L., North, K., Ouvrier, R., Ryan, M. (2008). Hand involvement in children with Charcot-Marie-Tooth disease type 1A. Neuromuscular Disorders, 18(12), 970-973. [More Information]

2006

  • Bray, P., Bundy, A. (2006). Experience sampling methodology in children with neuromuscular disorders: A feasibility study. Fifth Research Conference 2006. University of Sydney.

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