scholarly article | Q13442814 |
P2093 | author name string | Mari Tsuruwaka | |
Rieko Yokose | |||
P2860 | cites work | Whose job? The staffing of advance care planning support in twelve international healthcare organizations: a qualitative interview study. | Q55539851 |
Systematic Implementation of an Advance Directive Program in Nursing Homes | Q58854513 | ||
STEP: an intervention to address the issue of stigma related to leprosy in Southern Nepal | Q82256764 | ||
A broader understanding of care managers' attitudes of advance care planning: A concurrent nested design | Q88728604 | ||
Physicians' Views on Advance Care Planning and End-of-Life Care Conversations | Q88802965 | ||
The impact of advance care planning on end of life care in elderly patients: randomised controlled trial | Q24614583 | ||
Advance care planning: A systematic review of randomised controlled trials conducted with older adults | Q26741914 | ||
Advance Care Planning Discussions: Why They Should Happen, Why They Don't, and How We Can Facilitate the Process | Q26797505 | ||
Whatever happened to qualitative description? | Q34001833 | ||
Disability in people affected by leprosy: the role of impairment, activity, social participation, stigma and discrimination | Q34349274 | ||
Practical methods to increase use of advance medical directives | Q34749473 | ||
Perceived Stigma towards Leprosy among Community Members Living Close to Nonsomboon Leprosy Colony in Thailand | Q35654686 | ||
Lay and peer counsellors to reduce leprosy-related stigma--lessons learnt in Cirebon, Indonesia | Q35660797 | ||
Planning for the end of life: the views of older people about advance care statements | Q35746914 | ||
The effect of a social work intervention to enhance advance care planning documentation in the nursing home | Q36021191 | ||
'People like me don't make things like that': Participatory video as a method for reducing leprosy-related stigma | Q36028079 | ||
End-of-life expectations and experiences among nursing home patients and their relatives--a synthesis of qualitative studies | Q38224430 | ||
Defining Advance Care Planning for Adults: A Consensus Definition From a Multidisciplinary Delphi Panel | Q38773764 | ||
Assessing a nurse-led advance directive and advance care planning seminar | Q44940262 | ||
Courtesy stigma: A concealed consternation among caregivers of people affected by leprosy | Q47590989 | ||
Palliative assessment and advance care planning in severe dementia: an exploratory randomized controlled trial of a complex intervention | Q48710394 | ||
The Journey to Interprofessional Collaborative Practice: Are We There Yet? | Q49652399 | ||
Illness perceptions of leprosy-cured individuals in Surinam with residual disfigurements - "I am cured, but still I am ill". | Q50198143 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 3 | |
P304 | page(s) | 199-217 | |
P577 | publication date | 2018-08-03 | |
P1433 | published in | Asian Bioethics Review | Q56753884 |
P1476 | title | Barriers to Promoting Advance Care Planning for Residents Living in a Sanatorium for Hansen's Disease: A Qualitative Study of Residents and Staff in Japan | |
P478 | volume | 10 |
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