A

Amsters, Delena, Schuurs, Sarita, Kendall, Melissa, Pershouse, Kiley, Barker, Ruth, and Kuipers, Pim (2014) General practice visits by people with traumatic spinal cord injury: a Queensland longitudinal study. Australian Journal of Primary Health, 20 (2). pp. 167-173.

B

Bhandari, A., van Dooren, K., Eastgate, G., Lennox, N., and Kinner, S.A. (2015) Comparison of social circumstances, substance use and substance-related harm in soon-to-be-released prisoners with and without intellectual disability. Journal of Intellectual Disability Research, 59 (6). pp. 571-579.

Bohanna, India, Catherall, Juliette, and Dingwall, Kylie (2013) Ensuring Indigenous Australians with acquired brain injuries have equitable access to the National Disability Insurance Scheme. Australian and New Zealand Journal of Public Health, 37 (6). p. 587.

Bohanna, India, Stephens, Anne, Wargent, Rachael, Catherall, Juliette, Timms, Carolyn, Graham, Deborah, and Clough, Alan (2013) Assessment of acquired brain injury in Aboriginal and Torres Strait Islander Australians: guidance for DisabilityCare Australia. Report. James Cook University, Cairns, QLD.

Barker, R., Pershouse, K., Kendall, M., and Amsters, D. (2008) The relationship between quality of life and ICF components of function and disability for people with spinal cord injury. In: 2007 APA Conference Week Abstracts: national neurology group conference: hot topics in the tropics (54) S11-S11. From: 2007 APA Conference Week: national neurology group conference: hot topics in the tropics, 4-8 October 2007, Cairns, QLD, Australia.

Barker, Ruth N., Amsters, Delena I., Kendall, Melissa D., Pershouse, Kiley J., and Haines, Terry P. (2007) Reliability of the clinical outcome variables scale when administered via telephone to assess mobility in people with spinal cord injury. Archives of Physical Medicine and Rehabilitation, 88 (5). pp. 632-637.

C

Cohen, Libby, and Brown, Roy I. (2012) Mapping future research in disabilities-research initiatives in intellectual disabilities in India: report of a national interdisciplinary meeting. Journal of Policy and Practice in Intellectual Disabilities, 9 (2). pp. 151-155.

D

Davis, Elise, Mackinnon, Andrew, Davern, Melanie, Boyd, Roslyn, Bohanna, India, Waters, Elizabeth, Graham, H. Kerr, Reid, Susan, and Reddihough, Dinah (2013) Description and psychometric properties of the CP QOL-Teen: a quality of life questionnaire for adolescents with cerebral palsy. Research in Developmental Disabilities, 34 (1). pp. 344-352.

E

Eley, D.S., Boyes, J., Young, L., and Hegney, D.G. (2009) Accommodation needs for carers of and adults with intellectual disability in regional Australia: their hopes for and perceptions of the future. Rural and Remote Health, 9. 1239. pp. 1-13.

Eley, Diann, Boyes, Joanne, Young, Louise, and Hegney, Desley (2009) Adults with intellectual disability in regional Australia: Incidence of disability and provision of accommodation support to their ageing carers. Australian Journal of Rural Health, 17 (3). pp. 161-166.

H

Hayles, Emily, Jones, Anne, Harvey, Desley, Plummer, David, and Ruston, Sally (2015) Delivering healthcare services to children with cerebral palsy and their families: a narrative review. Health and Social Care in the Community, 23 (3). pp. 242-251.

Hayles, Emily, Harvey, Desley, Plummer, David, and Jones, Anne (2015) Parents' experiences of health care for their children with cerebral palsy. Qualitative Health Research, 25 (8). pp. 1139-1154.

Hayles, Emily R. (2014) "Making the most of their body and their life": parents' experiences of health care for their children with cerebral palsy. Masters (Research) thesis, James Cook University.

Hansen, R., Tresse, S., and Gunnarsson, R.K. (2004) Fewer accidents and better maintenance with active wheelchair check-ups: a randomized controlled clinical trial. Clinical Rehabilitation, 18. pp. 631-639.

L

Lloyd, Janice, Johnston, Laura, and Lewis, Julia (2018) Towards a better understanding of the psychiatric assistance dog team. In: Abstracts from the Australasian Mental Health and Higher Education Conference. p. 28. From: 2nd Australasian Mental Health and Higher Education Conference, 6-7 July 2018, Townsville, QLD, Australia.

Lim, Kah Heng Alexander, Speare, Rick, Thomas, Gail, and Graves, Patricia (2015) Surgical treatment of genital manifestations of lymphatic filariasis: a systematic review. World Journal of Surgery, 39 (12). pp. 2885-2899.

P

Pearn, John, and Franklin, Richard C. (2013) Disability and drowning: personal experiences, research, and practicalities of adapted aquatics. International Journal of Aquatic Research and Education, 7 (2). pp. 157-162.

Pershouse, Kiley J., Barker, Ruth N., Kendall, Melissa B., Buettner, Petra G., Kuipers, Pim, Schuurs, Sarita B., and Amsters, Delena I. (2012) Investigating changes in quality of life and function along the lifespan for people with spinal cord injury. Archives of Physical Medicine and Rehabilitation, 93 (3). pp. 413-419.

Parker, Malorie G., and Yau, Matthew K. (2012) Sexuality, identity and women with spinal cord injury. Sexuality and Disability, 30 (1). pp. 15-27.

R

Rasalam, Roy (2020) Communicating with people who have an intellectual disability disorder about their diabetes: a guide for health professionals. Australian Diabetes Educator, 23 (2).

S

Stephens, Anne, Cullen, Jennifer, Massey, Libby, and Bohanna, India (2014) Will the National Disability Insurance Scheme improve the lives of those most in need? Effective service delivery for people with acquired brain injury and other disabilities in remote Aboriginal and Torres Strait Islander communities. Australian Journal of Public Administration, 73 (2). pp. 260-270.

Stephens, Anne, and Bohanna, India (2013) Why indigenous Australians need a properly funded NDIS. The Conversation, 18 December 2013.

Scurrah, Alena, Sheppard, Lorraine, and Buttner, Petra (2009) Effects of introducing an allied health assessment pro-forma on the management of acute stroke patients. Disability and Rehabilitation, 31 (5). pp. 1293-1299.

T

Tuominen- Eriksson, Alli-Marie, Svensson, Yvonne, and Gunnarsson, Ronny K. (2013) Children with disabilities are often misdiagnosed initially and children with neuropsychiatric disorders are referred to adequate resources 30 months later than children with other disabilities. Journal of Autism and Developmental Disorders, 43 (3). pp. 579-584.

V

Vaz, Sharmila, Cordier, Reinie, Falkmer, Marita, Ciccarelli, Marina, Parsons, Richard, McAuliffe, Tomomi, and Falkmer, Torbjorn (2015) Should schools expect poor physical and mental health, social adjustment, and participation outcomes in students with disability? PLoS One, 10 (5). e0126630. pp. 1-23.

W

Wielandt, Trish, McKenna, Kryss, Tooth, Leigh, and Strong, Jenny (2006) Factors that predict the post-discharge use of recommended assistive technology (AT). Disability and Rehabilitation: Assistive Technology, 1 (1-2). pp. 29-40.

Y

Young, Louise (2006) Community and cluster centre residential services for adults with intellectual disability: long-term results from an Australian-matched sample. Journal of Intellectual Disability Research, 50 (6). pp. 419-431.

Ypinazar, Valmae Anne (2003) This is our life, this is our child: mothers dancing in the margins of disability. PhD thesis, James Cook University.

Z

Zeldenryk, Lynne, Gray, Marion, Gordon, Susan, Speare, Rick, and Hossain, Moazzem (2014) The use of focus groups to develop a culturally relevant quality of life tool for lymphatic filariasis in Bangladesh. Quality of Life Research, 23 (1). pp. 299-309.

Zeldenryk, Lynne Michelle (2013) Measuring the impact of lymphatic filariasis: the development of a quality of life tool using mixed methods. PhD thesis, James Cook University.