Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Milberg, Anna
and
Strang, Peter
2004.
Exploring comprehensibility and manageability in palliative home care: An interview study of dying cancer patients' informal carers.
Psycho-Oncology,
Vol. 13,
Issue. 9,
p.
605.
Appelin, Gunilla
Brobäck, Gunilla
and
Berterö, Carina
2005.
A comprehensive picture of palliative care at home from the people involved.
European Journal of Oncology Nursing,
Vol. 9,
Issue. 4,
p.
315.
Goldschmidt, Dorthe
Schmidt, Lone
Krasnik, Allan
Christensen, Ulla
and
Groenvold, Mogens
2006.
Expectations to and evaluation of a palliative home-care team as seen by patients and carers.
Supportive Care in Cancer,
Vol. 14,
Issue. 12,
p.
1232.
Milberg, A.
and
Strang, P.
2007.
What to do when ‘there is nothing more to do’? A study within a salutogenic framework of family members' experience of palliative home care staff.
Psycho-Oncology,
Vol. 16,
Issue. 8,
p.
741.
MELIN-JOHANSSON, C
AXELSSON, B.
and
DANIELSON, E.
2007.
Caregivers? perceptions about terminally ill family members? quality of life.
European Journal of Cancer Care,
Vol. 16,
Issue. 4,
p.
338.
Palm, Inger
and
Friedrichsen, Maria
2008.
The lived experience of closeness in partners of cancer patients in the home care setting.
International Journal of Palliative Nursing,
Vol. 14,
Issue. 1,
p.
6.
Rydé, Kerstin
Strang, Peter
and
Friedrichsen, Maria
2008.
Crying in Solitude or With Someone for Support and Consolation-Experiences From Family Members in Palliative Home Care.
Cancer Nursing,
Vol. 31,
Issue. 5,
p.
345.
Milberg, Anna
Olsson, Eva-Carin
Jakobsson, Maria
Olsson, Maria
and
Friedrichsen, Maria
2008.
Family Members' Perceived Needs for Bereavement Follow-Up.
Journal of Pain and Symptom Management,
Vol. 35,
Issue. 1,
p.
58.
Van Puymbroeck, Marieke
Sberna Hinojosa, Melanie
and
Rittman, Maude R.
2008.
Influence of Sense of Coherence on Caregiver Burden and Depressive Symptoms at 12 Months Poststroke.
Topics in Stroke Rehabilitation,
Vol. 15,
Issue. 3,
p.
272.
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.
Skott, Carola
and
Lundgren, Solveig M
2009.
Complexity and contradiction: home care in a multicultural area.
Nursing Inquiry,
Vol. 16,
Issue. 3,
p.
223.
Waldrop, Deborah P.
and
Rinfrette, Elaine S.
2009.
Can short hospice enrollment be long enough? Comparing the perspectives of hospice professionals and family caregivers.
Palliative and Supportive Care,
Vol. 7,
Issue. 1,
p.
37.
Linderholm, Märit
and
Friedrichsen, Maria
2010.
A Desire to Be Seen.
Cancer Nursing,
Vol. 33,
Issue. 1,
p.
28.
Sand, Lisa
Olsson, Mariann
and
Strang, Peter
2010.
What are motives of family members who take responsibility in palliative cancer care?.
Mortality,
Vol. 15,
Issue. 1,
p.
64.
Milberg, Anna
and
Strang, Peter
2011.
Protection against perceptions of powerlessness and helplessness during palliative care: The family members' perspective.
Palliative and Supportive Care,
Vol. 9,
Issue. 3,
p.
251.
Milberg, Anna
Appelquist, Gudrun
Hagelin, Ewa
Jakobsson, Maria
Olsson, Eva-Carin
Olsson, Maria
and
Friedrichsen, Maria
2011.
“A rewarding conclusion of the relationship”: staff members’ perspectives on providing bereavement follow-up.
Supportive Care in Cancer,
Vol. 19,
Issue. 1,
p.
37.
Carlsson, Maria E.
2012.
Sleep disturbance in relatives of palliative patients cared for at home.
Palliative and Supportive Care,
Vol. 10,
Issue. 3,
p.
165.
Waldrop, Deborah P.
Meeker, Mary Ann
Kerr, Christopher
Skretny, Judith
Tangeman, John
and
Milch, Robert
2012.
The Nature and Timing of Family-Provider Communication in Late-Stage Cancer: A Qualitative Study of Caregivers’ Experiences.
Journal of Pain and Symptom Management,
Vol. 43,
Issue. 2,
p.
182.
Henriksson, Annette
Andershed, Birgitta
Benzein, Eva
and
Årestedt, Kristofer
2012.
Adaptation and psychometric evaluation of the Preparedness for Caregiving Scale, Caregiver Competence Scale and Rewards of Caregiving Scale in a sample of Swedish family members of patients with life-threatening illness.
Palliative Medicine,
Vol. 26,
Issue. 7,
p.
930.
Henriksson, Anette
Årestedt, Kristofer
Benzein, Eva
Ternestedt, Britt-Marie
and
Andershed, Birgitta
2013.
Effects of a support group programme for patients with life-threatening illness during ongoing palliative care.
Palliative Medicine,
Vol. 27,
Issue. 3,
p.
257.