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 49
Healthcare utilization among breast cancer patients during the COVID-19 outbreak
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- Published online by Cambridge University Press:
- 29 June 2020, pp. 385-391
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- Cited by 49
An open trial of aripiprazole for the treatment of delirium in hospitalized cancer patients
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- Published online by Cambridge University Press:
- 22 November 2011, pp. 351-357
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- Cited by 49
Meaning of life, representation of death, and their association with psychological distress
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- Published online by Cambridge University Press:
- 09 August 2017, pp. 511-519
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- Cited by 49
Course of distress, anxiety, and depression in hematological cancer patients: Association between gender and grade of neoplasm
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- 04 November 2013, pp. 115-123
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- Cited by 48
Sleep disturbances in caregivers of patients with advanced cancer: A systematic review.
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- 18 January 2017, pp. 125-140
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- Cited by 48
Urban voices: The quality-of-life experience among women of color with breast cancer
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- 22 May 2007, pp. 115-125
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- Cited by 48
Knowledge of advance directive and perceptions of end-of-life care in Chinese-American elders: The role of acculturation
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- 11 June 2015, pp. 1677-1684
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- Cited by 48
Losing a parent to cancer: A preliminary investigation into the needs of adolescents and young adults
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- 27 September 2010, pp. 255-265
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- Cited by 47
What makes grief difficult? Perspectives from bereaved family caregivers and healthcare providers of advanced cancer patients
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- 27 September 2010, pp. 277-289
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- Cited by 47
Preliminary study of themes of meaning and psychosocial service use among informal cancer caregivers
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- 07 August 2013, pp. 139-148
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- Cited by 46
Involvement in everyday life for people with a life threatening illness
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- 27 September 2010, pp. 345-352
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- Cited by 46
A national approach to improving adolescent and young adult (AYA) oncology psychosocial care: The development of AYA-specific psychosocial assessment and care tools
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- 10 May 2013, pp. 183-188
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- Cited by 46
Experiences of engagement in creative activity at a palliative care facility
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- 24 September 2007, pp. 241-250
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- Cited by 46
Affirming the right to care, preserving the right to die: Disorders of consciousness and neuroethics after Schiavo
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- 09 August 2006, pp. 169-178
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- Cited by 46
Advance care planning in advanced cancer: Can it be achieved? An exploratory randomized patient preference trial of a care planning discussion
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- 25 February 2011, pp. 3-13
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- Cited by 46
Exercise interventions for patients with advanced cancer: A systematic review of recruitment, attrition, and exercise adherence rates
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- 21 May 2019, pp. 686-696
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- Cited by 46
The experiences, coping mechanisms, and impact of death and dying on palliative medicine specialists
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- 11 June 2013, pp. 309-316
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- Cited by 45
Integration of Latino/a cultural values into palliative health care: A culture centered model
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- 17 June 2013, pp. 149-157
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- Cited by 45
Spiritual AIM and the work of the chaplain: A model for assessing spiritual needs and outcomes in relationship
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- 10 March 2014, pp. 75-89
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- Cited by 45
Training for awareness of one's own spirituality: A key factor in overcoming barriers to the provision of spiritual care to advanced cancer patients by doctors and nurses
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- 06 September 2018, pp. 345-352
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