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 21
Facing uncertainty: The lived experience of palliative care
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- Published online by Cambridge University Press:
- 24 September 2007, pp. 255-264
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- Cited by 21
Voicing their choices: Advance care planning with adolescents and young adults with cancer and other serious conditions
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- Published online by Cambridge University Press:
- 03 December 2021, pp. 462-470
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- Cited by 21
A feasibility and acceptability study of an adaptation of the Mindful Self-Compassion program for adult cancer patients
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- 09 October 2019, pp. 130-140
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- Cited by 21
Early integration of palliative care in a long-term care home: A telemedicine feasibility pilot study
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- 18 February 2020, pp. 460-467
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- Cited by 21
Seventeen years of progress for supportive care services: A resurvey of National Cancer Institute–designated comprehensive cancer centers
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- 03 July 2014, pp. 917-925
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- Cited by 21
An examination of Latino-advanced cancer patients' and their informal caregivers' preferences for communication about advance care planning: A qualitative study
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- 08 November 2019, pp. 277-284
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A feasibility study of a two-session home-based cognitive behavioral therapy–insomnia intervention for bereaved family caregivers
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- 18 June 2009, pp. 197-206
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- Cited by 21
Recovering function and surviving treatments are primary motivators for health behavior change in patients with head and neck cancer: Qualitative focus group study
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- 23 November 2015, pp. 364-375
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- Cited by 21
Communication for end-of-life care planning among Korean patients with terminal cancer: A context-oriented model
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- 03 July 2015, pp. 69-76
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- Cited by 21
Validation of the Family Inventory of Needs (FIN) for family caregivers in palliative care
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- 20 May 2014, pp. 485-491
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- Cited by 21
Persistence of psychological distress and correlated factors among patients with head and neck cancer
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- 19 June 2015, pp. 42-51
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- Cited by 21
A standardized low-cost peer role-playing training intervention improves medical student competency in communicating bad news to patients in Botswana
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- 17 October 2018, pp. 60-65
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Distress and body image due to altered appearance in posttreatment and active treatment of breast cancer patients and in general population controls
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- 06 March 2017, pp. 137-145
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- Cited by 21
Chemotherapeutic drugs that penetrate the blood–brain barrier affect the development of hyperactive delirium in cancer patients
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- 26 June 2014, pp. 859-864
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- Cited by 21
Experiences of truth disclosure in terminally ill cancer patients in palliative home care
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- 04 May 2011, pp. 173-180
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Providing care and sharing expertise: Reflections of nurse-specialists in palliative home care
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- 30 September 2009, pp. 357-364
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Actigraphy as an assessment of performance status in patients with advanced lung cancer
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- 11 February 2019, pp. 574-578
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- Cited by 21
Comparing the distress thermometer (DT) with the patient health questionnaire (PHQ)-2 for screening for possible cases of depression among patients newly diagnosed with advanced cancer
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- 13 November 2013, pp. 63-68
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- Cited by 21
Aromatase inhibitors and mood disturbances
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- 08 June 2012, pp. 225-227
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- Cited by 21
Predisposing and precipitating risk factors for delirium in palliative care patients
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- 14 November 2019, pp. 437-446
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