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Volumn 19, Issue 3, 2007, Pages 355-362
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What real outcomes matter to caregivers?
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Author keywords
Alzheimer's disease; Alzheimer's organizations; Burden of care; Caregivers' needs; Dementia; Social research
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Indexed keywords
CAREGIVER BURDEN;
COGNITION;
CONFERENCE PAPER;
DEMENTIA;
EARLY DIAGNOSIS;
GENERAL PRACTITIONER;
HEALTH SURVEY;
HUMAN;
OUTCOME ASSESSMENT;
PAIN;
PALLIATIVE THERAPY;
PATIENT CARE;
POLAND;
TRAINING;
UNITED KINGDOM;
AGED;
ALZHEIMER DISEASE;
CAREGIVERS;
CONSUMER ORGANIZATIONS;
CONSUMER SATISFACTION;
COST OF ILLNESS;
CROSS-CULTURAL COMPARISON;
GREAT BRITAIN;
HEALTH SERVICES ACCESSIBILITY;
HEALTH SERVICES NEEDS AND DEMAND;
HEALTH SURVEYS;
HUMANS;
PALLIATIVE CARE;
POLAND;
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EID: 34248232639
PISSN: 10416102
EISSN: 1741203X
Source Type: Journal
DOI: 10.1017/S1041610207004851 Document Type: Conference Paper |
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Times cited : (7)
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References (0)
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