| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
Aged parents’ experiences during a critical illness trajectory and after the death of an adult child: A review of the literature
|
Van Humbeeck, Liesbeth
|
|
2013
|
27 |
7 |
p. 583-595
|
article
|
| 2 |
A multicenter survey of Hispanic caregiver preferences for patient decision control in the United States and Latin America
|
Yennurajalingam, Sriram
|
|
2013
|
27 |
7 |
p. 692-698
|
article
|
| 3 |
Bereaved relatives’ perspectives of the patient’s oral intake towards the end of life: A qualitative study
|
Raijmakers, Natasja JH
|
|
2013
|
27 |
7 |
p. 665-672
|
article
|
| 4 |
Death with dignity from the perspective of the surviving family: A survey study among family caregivers of deceased older adults
|
van Gennip, Isis E
|
|
2013
|
27 |
7 |
p. 616-624
|
article
|
| 5 |
Exploring factors and caregiver outcomes associated with feelings of preparedness for caregiving in family caregivers in palliative care: A correlational, cross-sectional study
|
Henriksson, Anette
|
|
2013
|
27 |
7 |
p. 639-646
|
article
|
| 6 |
Family caregiver learning—how family caregivers learn to provide care at the end of life: A qualitative secondary analysis of four datasets
|
Stajduhar, Kelli I
|
|
2013
|
27 |
7 |
p. 657-664
|
article
|
| 7 |
Family caregiver satisfaction with home-based nursing and physician care over the palliative care trajectory: Results from a longitudinal survey questionnaire
|
Guerriere, Denise N
|
|
2013
|
27 |
7 |
p. 632-638
|
article
|
| 8 |
Improving support for family carers: Key implications for research, policy and practice
|
Hudson, Peter
|
|
2013
|
27 |
7 |
p. 581-582
|
article
|
| 9 |
Informal hospice caregiver pain management concerns: A qualitative study
|
Kelley, Marjorie
|
|
2013
|
27 |
7 |
p. 673-682
|
article
|
| 10 |
Living with breathlessness: A survey of caregivers of breathless patients with lung cancer or heart failure
|
Malik, Farida A
|
|
2013
|
27 |
7 |
p. 647-656
|
article
|
| 11 |
Signs of post-traumatic stress disorder in caregivers following an expected death: A qualitative study
|
Sanderson, Christine
|
|
2013
|
27 |
7 |
p. 625-631
|
article
|
| 12 |
Spouse caregivers of people with advanced dementia in nursing homes: A longitudinal narrative study
|
Hennings, Jean
|
|
2013
|
27 |
7 |
p. 683-691
|
article
|
| 13 |
Tools to measure quality of life and carer burden in informal carers of heart failure patients: A narrative review
|
Whittingham, Katharine
|
|
2013
|
27 |
7 |
p. 596-607
|
article
|
| 14 |
Towards better support for family carers: A richer understanding
|
Payne, Sheila
|
|
2013
|
27 |
7 |
p. 579-580
|
article
|
| 15 |
Uncovering an invisible network of direct caregivers at the end of life: A population study
|
Burns, Catherine M
|
|
2013
|
27 |
7 |
p. 608-615
|
article
|
Journal description