Browse by ANZSRC Socio-Economic Objective codes
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Hanks, Heather, Veitch, P. Craig, and Harris, Mark F. (2008) A rural/urban comparison of the roles of the general practitioner in colorectal cancer management. Australian Journal of Rural Health, 16 (6). pp. 376-382.
Hanks, Heather, Veitch, Craig, and Harris, Mark (2008) Colorectal cancer management - the role of the GP. Australian Family Physician, 37 (4). pp. 259-261.
Howat, A., Veitch, C., and Cairns, W. (2007) A retrospective review of place of death of palliative care patients in regional north Queensland. Palliative Medicine, 21 (1). pp. 41-47.
Janda, Monika, Steginga, Suzanne, Dunn, Jeff, Langbecker, Danette, Walker, David, and Eakin, Elizabeth (2008) Unmet supportive care needs and interests in services among patients with a brain tumour and their carers. Patient Education and Counseling, 71 (2). pp. 251-258.
Love , Anthony, Street, Annette, Ray, Robin, Harris, Rod, and Lowe, Roger (2005) Social aspects of caregiving for people living with motor neurone disease: their relationships to carer wellbeing. Palliative and Supportive Care, 3 (1). pp. 33-38.
O'Connor, Lera, Gardner, Anne, Millar, Lynne, and Bennett, Peter (2009) Absolutely fabulous—But are we? Carers’ perspectives on satisfaction with a palliative homecare service. Collegian, 16 (4). pp. 201-209.
O'Connor, Lera, Bennett, Peter, Gardner, Anne, Hawkins, Mary T., and Wellman, David (2009) Implementing a journal club in a palliative care setting: a link in the chain of evidence-based practice. Collegian, 16 (3). pp. 147-152.
Ray, Robin A., and Street, Annette F. (2011) The dynamics of socio-connective trust within support networks accessed by informal caregivers. Health, 15 (2). pp. 137-152.
Ray, R., and Brown, J. (2009) Managing death in ALS/MND: identifying caregivers' perspectives of the final days of life. Proceedings of 20th International Symposium on ALS/MND 20th International Symposium on ALS/MND. , 8 - 10 December, 2009, Berlin, Germany.
Ray, Robin A., and Street, Annette F. (2007) Nonfinite loss and emotional labour: family caregivers' experiences of living with motor neurone disease. Journal of Clinical Nursing, 16 (3a). pp. 35-43.
Ray, Robin A., and Street, Annette F. (2006) Caregiver bodywork: family member's experiences of caring for someone living with motor neurone disease (MND). Journal of Advanced Nursing, 56 (1). pp. 35-43.
Ray, Robin (2006) "It's all down hill from here," or is it? Living with loss and grief associated with motor neurone disease. Grief Matters: The Australian Journal of Grief and Bereavement, 9 (1). pp. 8-11.
Ray, R.A., Street, A.F., and Love , A.W. (2006) The impact of ambiguous loss and emotional labour on family carers. Amyotrophic Lateral Sclerosis, 7 (s1). pp. 19-21.
Ray, Robin A., and Street, Annette F. (2005) Who's there and who cares: age as an indicator of social support networks for caregivers among people living with motor neurone disease. Health and Social Care in the Community, 13 (6). pp. 542-552.
Ray, R.A., Street, A.F., and Love, A.W. (2005) Engaging social support systems to improve quality of life for patients and carers. Amyotrophic Lateral Sclerosis, 6 (s1). pp. 36-38.
Ray, Robin A., Brown, Janice, and Street, Annette F. Dying with motor neurone disease, what can we learn from family caregivers? Health Expectations . pp. 1-11. (In Press)