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 30
Bereaved spouses' adjustment after the patients' death in palliative care
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- Published online by Cambridge University Press:
- 25 October 2007, pp. 397-404
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- Cited by 29
Experience of anxiety among patients with severe COPD: A qualitative, in-depth interview study
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- Published online by Cambridge University Press:
- 06 August 2013, pp. 465-472
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Do spirituality and faith make a difference? Report from the Southern European Psycho-Oncology Study Group
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- Published online by Cambridge University Press:
- 28 September 2010, pp. 405-413
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- Cited by 29
The experience of being an informal “carer” for a person with cancer: A meta-synthesis of qualitative studies
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- Published online by Cambridge University Press:
- 10 March 2014, pp. 493-504
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Use of an electronic patient-reported outcome measurement system to improve distress management in oncology
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- 16 October 2013, pp. 69-73
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Consistency of symptom clusters among advanced cancer patients seen at an outpatient supportive care clinic in a tertiary cancer center
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- 07 February 2013, pp. 473-480
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Specialized palliative care in advanced cancer: What is the efficacy? A systematic review
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- 13 June 2017, pp. 724-740
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Advance care planning in different settings for people with dementia: A systematic review and narrative synthesis
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- 10 June 2019, pp. 707-719
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A feasibility study of Dignity Psychotherapy delivered via telemedicine
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- 04 April 2005, pp. 149-155
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Documenting presence: A descriptive study of chaplain notes in the intensive care unit
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- 20 June 2016, pp. 190-196
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Caring for terminally ill Muslim patients: Lived experiences of non-Muslim nurses
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- Published online by Cambridge University Press:
- 20 April 2016, pp. 599-611
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- Cited by 29
Depression and anxiety in palliative care inpatients compared with those receiving palliative care at home
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- 22 November 2011, pp. 393-400
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The meaning of being in transition to end-of-life care for female partners of spouses with cancer
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- 26 November 2009, pp. 423-433
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Health care professionals' perspectives of living and dying with primary malignant glioma: Implications for a unique cancer trajectory
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- 21 October 2013, pp. 1519-1527
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- Cited by 29
At the crossroads: Making the transition to hospice
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- 19 July 2005, pp. 351-360
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- Cited by 29
Burnout among physicians in palliative care: Impact of clinical settings
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- 14 October 2015, pp. 402-410
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A systematic review of instruments assessing dimensions of distress among caregivers of adult and pediatric cancer patients
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- Published online by Cambridge University Press:
- 29 March 2016, pp. 110-124
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- Cited by 28
A comparison of patients dying at home and patients dying at a hospice: Sociodemographic factors and caregivers' experiences
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- 29 April 2003, pp. 33-39
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- Cited by 28
Should symptoms be scaled for intensity, frequency, or both?
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- 29 April 2003, pp. 51-60
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- Cited by 28
Aligning guidelines and medical practice: Literature review on pediatric palliative care guidelines
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- 09 January 2017, pp. 474-489
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