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Menne, H. L., Bass, D. M., Johnson, J. D., Primetica, B., Kearney, K. R., Bollin, S., Molea, M. J., & Teri, L. (2014). Statewide implementation of "Reducing Disability of Alzheimer's Disease”: Impact on family caregiver outcomes. Journal of Gerontological Social Work, 57(6/7), 626-639. doi:10.1080/01634372.2013.870276

Noelker, L. S., & Bass, D. M. (1994). Relationships between the frail elderly's informal and formal helpers. In E. Kahana, D. Biegel, & M. Wykle (Eds.), Family caregiving across the lifespan (pp. 356-381). New York: Sage Publications.

Moon, H., Townsend, A. L., Whitlatch, C. J., & Dilworth-Anderson, P. (2017). Quality of life for dementia caregiving dyads: Effects of incongruent perceptions of everyday care and values. The Gerontologist, 57(4), 657-666. doi:10.1093/geront/gnw055

Aneshensel, C. S., Pearlin, L.I ., Mullan, J. T., Zarit, S. H., & Whitlatch, C. J. (1995). Profiles in caregiving: The unexpected career. San Diego: Academic Press.

Deimling, G. T. & Looman, W. J. (1993). Predictors of the use of respite services by caregivers of Alzheimer's patients: Racial and generational differences. Sociological Practice, 11(1), 158-175.