Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Wong, W. K. Tim
and
Ussher, Jane
2009.
Bereaved informal cancer carers making sense of their palliative care experiences at home.
Health & Social Care in the Community,
Vol. 17,
Issue. 3,
p.
274.
Keesing, Sharon
Rosenwax, Lorna
and
McNamara, Beverley
2011.
‘Doubly deprived’: a post-death qualitative study of primary carers of people who died in Western Australia.
Health & Social Care in the Community,
Vol. 19,
Issue. 6,
p.
636.
Hudson, Peter
and
Payne, Sheila
2011.
Family Caregivers and Palliative Care: Current Status and Agenda for the Future.
Journal of Palliative Medicine,
Vol. 14,
Issue. 7,
p.
864.
PERZ, J.
USSHER, J.M.
BUTOW, P.
and
WAIN, G.
2011.
Gender differences in cancer carer psychological distress: an analysis of moderators and mediators.
European Journal of Cancer Care,
Vol. 20,
Issue. 5,
p.
610.
Ussher, Jane M.
Tim Wong, W.K.
and
Perz, Janette
2011.
A qualitative analysis of changes in relationship dynamics and roles between people with cancer and their primary informal carer.
Health: An Interdisciplinary Journal for the Social Study of Health, Illness and Medicine,
Vol. 15,
Issue. 6,
p.
650.
Merluzzi, Thomas V.
Philip, Errol J.
Vachon, Dominic O.
and
Heitzmann, Carolyn A.
2011.
Assessment of self-efficacy for caregiving: The critical role of self-care in caregiver stress and burden.
Palliative and Supportive Care,
Vol. 9,
Issue. 1,
p.
15.
Levesque, Janelle V.
and
Maybery, Darryl
2012.
Parental Cancer.
Qualitative Health Research,
Vol. 22,
Issue. 3,
p.
397.
Kang, Jina
Shin, Dong Wook
Choi, Ji Eun
Sanjo, Makiko
Yoon, Soo Jin
Kim, Hwan Kyun
Oh, Myoung Suk
Kwen, Hyang Suk
Choi, Hae Young
and
Yoon, Wook Hee
2013.
Factors associated with positive consequences of serving as a family caregiver for a terminal cancer patient.
Psycho-Oncology,
Vol. 22,
Issue. 3,
p.
564.
Kim, Youngmee
Carver, Charles S.
Schulz, Richard
Lucette, Aurelie
and
Cannady, Rachel S.
2013.
Finding Benefit in Bereavement among Family Cancer Caregivers.
Journal of Palliative Medicine,
Vol. 16,
Issue. 9,
p.
1040.
Kim, Youngmee
Lucette, Aurelie
and
Loscalzo, Matthew
2013.
Bereavement Needs of Adults, Children, and Families After Cancer.
The Cancer Journal,
Vol. 19,
Issue. 5,
p.
444.
Teixeira, Ricardo J.
and
Pereira, M. Graça
2013.
Factors Contributing to Posttraumatic Growth and Its Buffering Effect in Adult Children of Cancer Patients Undergoing Treatment.
Journal of Psychosocial Oncology,
Vol. 31,
Issue. 3,
p.
235.
Cassidy, Tony
2013.
Benefit finding through caring: The cancer caregiver experience.
Psychology & Health,
Vol. 28,
Issue. 3,
p.
250.
Li, Qiuping
and
Loke, Alice Yuen
2013.
The positive aspects of caregiving for cancer patients: a critical review of the literature and directions for future research.
Psycho-Oncology,
Vol. 22,
Issue. 11,
p.
2399.
Lund, Line
Ross, Lone
Petersen, Morten Aagaard
and
Groenvold, Mogens
2014.
Cancer caregiving tasks and consequences and their associations with caregiver status and the caregiver’s relationship to the patient: a survey.
BMC Cancer,
Vol. 14,
Issue. 1,
Stenberg, Una
Ekstedt, Mirjam
Olsson, Mariann
and
Ruland, Cornelia M.
2014.
Living Close to a Person With Cancer: A Review of the International Literature and Implications for Social Work Practice.
Journal of Gerontological Social Work,
Vol. 57,
Issue. 6-7,
p.
531.
Edo‐Gual, Montserrat
Tomás‐Sábado, Joaquín
Bardallo‐Porras, Dolores
and
Monforte‐Royo, Cristina
2014.
The impact of death and dying on nursing students: an explanatory model.
Journal of Clinical Nursing,
Vol. 23,
Issue. 23-24,
p.
3501.
Bryson, Gregory L.
Mercer, Chris
and
Varpio, Lara
2014.
Patient and caregiver experience following ambulatory surgery: qualitative analysis in a cohort of patients 65 yr and older.
Canadian Journal of Anesthesia/Journal canadien d'anesthésie,
Vol. 61,
Issue. 11,
p.
986.
Sano, Tomomi
Kusajima, Etsuko
Shirai, Yuki
Setoyama, Mariko
Tamai, Terue
Hirooka, Kayo
Sato, Takahiro
Miyashita, Mitsunori
Kawa, Masako
and
Okabe, Takeshi
2014.
Personal growth and related factors among family primary caregivers after bereavement of a terminally ill cancer patient at home.
Palliative Care Research,
Vol. 9,
Issue. 3,
p.
140.
Peacock, Shelley
Duggleby, Wendy
and
Koop, Priscilla
2014.
The lived experience of family caregivers who provided end-of-life care to persons with advanced dementia.
Palliative and Supportive Care,
Vol. 12,
Issue. 2,
p.
117.
Levesque, Janelle V.
and
Maybery, Darryl J.
2014.
Predictors of Benefit Finding in the Adult Children of Patients with Cancer.
Journal of Psychosocial Oncology,
Vol. 32,
Issue. 5,
p.
535.