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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

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

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.

Menne, H. L., Judge, K. S., & Whitlatch, C. J. (2009). Predictors of quality of life for individuals with dementia: Implications for intervention. Dementia: The International Journal of Social Research and Practice, 8(4), 543-560. doi:10.1177/1471301209350288

Whitlatch, C. J., Feinberg, L. F., & Stevens, E. J. (1999). Predictors of institutionalization for persons with Alzheimer's disease and the impact on family caregivers. Journal of Mental Health and Aging, 5(3), 275-288.