Public Policy in MND Care: The Australian Perspective
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Publisher
Springer Singapore
Link
http://link.springer.com/content/pdf/10.1007/978-981-15-5840-5_2
Reference36 articles.
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3. Aoun, S.M., L.J. Breen, D. Oliver, R.D. Henderson et al. (2017a). Family carers’ experiences of receiving the news of a diagnosis of Motor Neurone Disease: A national survey. Journal of the Neurological Sciences 372: 144–51.
4. Aoun, S.M., K. Deas, L.J. Kristjanson, and D.W. Kissane (2017b). Identifying and addressing the support needs of family caregivers of people with motor neurone disease using the Carer Support Needs Assessment Tool. Palliative and Supportive Care 15 (1): 32–43.
5. Aoun, S. M., B. Rumbold, D. Howting, A. Bolleter, and L.J. Breen (2017c). Bereavement support for family caregivers: The gap between guidelines and practice in palliative care. PLoS One 12 (10): e0184750.
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