Most cited
This page lists all time most cited articles for this title. Please use the publication date filters on the left if you would like to restrict this list to recently published content, for example to articles published in the last three years. The number of times each article was cited is displayed to the right of its title and can be clicked to access a list of all titles this article has been cited by.
- Cited by 35
Art therapy among palliative cancer patients: Aesthetic dimensions and impacts on symptoms
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- Published online by Cambridge University Press:
- 20 November 2015, pp. 376-380
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- Cited by 35
The experience of adolescents who have a parent with advanced cancer: A phenomenological inquiry
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- Published online by Cambridge University Press:
- 03 September 2014, pp. 1057-1069
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- Cited by 35
Cancer and post-traumatic stress disorder: Diagnosis, pathogenesis and treatment considerations
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- Published online by Cambridge University Press:
- 22 March 2012, pp. 213-223
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- Cited by 35
Indigenous people's experiences at the end of life
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- Published online by Cambridge University Press:
- 15 June 2015, pp. 1721-1733
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- Cited by 35
On the road again: Patient perspectives on commuting for palliative care
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- Published online by Cambridge University Press:
- 23 March 2010, pp. 187-195
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- Cited by 35
Improving the Medical Assistance in Dying (MAID) process: A qualitative study of family caregiver perspectives
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- 19 March 2019, pp. 590-595
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- Cited by 35
Loneliness among cancer caregivers: A narrative review
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- 04 October 2019, pp. 359-367
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- Cited by 34
Quality of life among women after surgery for ovarian cancer
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- Published online by Cambridge University Press:
- 28 July 2008, pp. 239-247
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- Cited by 34
The surrogate's experience in authorizing a do not resuscitate order
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- Published online by Cambridge University Press:
- 19 February 2008, pp. 13-19
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- Cited by 34
Identifying and addressing the support needs of family caregivers of people with motor neurone disease using the Carer Support Needs Assessment Tool
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- Published online by Cambridge University Press:
- 13 May 2016, pp. 32-43
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- Cited by 34
Communication contexts about illness, death and dying for people with intellectual disabilities and life-limiting illness
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- 04 May 2011, pp. 201-208
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- Cited by 34
Delirium, agitation, and symptom distress within the final seven days of life among cancer patients receiving hospice care
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- 20 February 2014, pp. 211-216
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- Cited by 34
Advance care planning in motor neuron disease: A systematic review
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- 14 October 2015, pp. 411-432
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- Cited by 34
The meaning of quality of life: Narrations by patients with incurable cancer in palliative home care
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- 28 July 2008, pp. 231-238
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- Cited by 33
Assessing hope at the end of life: Validation of an experience of hope scale in advanced cancer patients
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- 12 May 2005, pp. 243-253
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- Cited by 33
A qualitative study of the trauma and posttraumatic growth of multiple myeloma patients treated with peripheral blood stem cell transplant
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- 25 October 2006, pp. 365-387
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- Cited by 33
Identification of patients with noncancer diseases for palliative care services
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- 24 August 2005, pp. 5-14
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- Cited by 33
Does social support from family and friends work as a buffer against reactions to stressful life events such as terminal cancer?
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- 27 February 2007, pp. 61-69
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- Cited by 33
Prognosticating futures and the human experience of hope
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- 24 September 2007, pp. 227-239
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- Cited by 33
Meeting the family: Measuring effectiveness of family meetings in a specialist inpatient palliative care unit
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- 13 February 2012, pp. 43-49
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