Browse by ANZSRC Socio-Economic Objective codes

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Group by: Creators | Item Type
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Number of items at this level: 18.

H

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.

J

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.

L

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

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.

R

Ray, Robin A., Brown, Janice, and Street, Annette F. (2014) Dying with motor neurone disease, what can we learn from family caregivers? Health Expectations, 17 (4). pp. 466-476.

Ray, Robin A., Fried, Ofra, and Lindsay, Daniel (2014) Palliative care professional education via video conference builds confidence to deliver palliative care in rural and remote locations. BMC Health Services Research, 14. pp. 1-8.

Ray, Robin, and Kavanagh, Anne (2014) Parkinson's disease, multiple sclerosis and motor neuron disease. In: Chang, Esther, and Johnson, Amanda, (eds.) Chronic Illness and Disability: principles for nursing practice. Elsevier, Sydney, NSW, Australia, pp. 329-350.

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. In: Proceedings of 20th International Symposium on ALS/MND (10), p. 35. From: 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.

This list was generated on Tue Mar 31 22:49:13 2015 EST.