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Whitlatch, C. J. (2001). Including the person with dementia in family care-giving research. Aging & Mental Health, 5(Suppl.1), S20-S22. doi:10.1080/713650016
Judge, K. S., Yarry, S. J., Looman, W. J., & Bass, D. M. (2013). Improved strain and psychosocial outcomes for caregivers of individuals with dementia: Findings from Project ANSWERS. The Gerontologist, 53(2), 280-292. doi:10.1093/geront/gns076
Noelker, L. S. & Harel, Z. (2000). Humanizing long-term care: Forging a link between quality of care and quality of life. In L. S. Noelker, & Z. Harel (Eds.), Linking quality of long-term care and quality of life (pp. 3-26). New York, NY: Springer.
Noelker, L. S., & Bass, D. M. (1989). Home care for elderly persons: Linkages between formal and informal caregivers. Journal of Gerontology, 44(2), S63-S70. doi:10.1093/geronj/44.2.S63
Deimling, G. T., Smerglia, V. L., & Barresi, C. M. (1990). Health care professionals and family involvement in care-related decisions concerning older patients. Journal of Aging and Health, 2(3), 310-325. doi:10.1177/089826439000200302