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Clark, P. A., Tucke, S. S., & Whitlatch, C. J. (2008). Consistency of information from persons with dementia: An analysis of differences by question type. Dementia: The International Journal of Social Research and Practice, 7(3), 341-358. doi:10.1177/1471301208093288

Gerace, C. S., & Noelker, L. S. (1990). Clinical social work practice with black elderly and their family caregivers. In Z. Harel, E. A. McKinney, & M. Williams (Eds.), Black aged: Understanding diversity and service needs (pp. 236-258). London: Sage Publications.

Schur, D. & Whitlatch, C. J. (2003). Circumstances leading to placement: A difficult caregiving decision. Lippincotts Case Management, 8(5), 187-197.

Bass, D. M., Garland, T. N., & Otto, M. E. (1985). Characteristics of hospice patients and their caregivers. Omega: Journal of Death and Dying, 16(1), 51-68. doi:10.2190/7MXX-TUM4-BMPA-KWV9

Bejjani, C., Snow, A. L., Judge, K. S., Bass, D. M., Morgan, R. O., Wilson, N., Walder, A., Looman, W. J., McCarthy, C., & Kunik, M. E. (2015). Characteristics of depressed caregivers of veterans with dementia. American Journal of Alzheimer's Disease and Other Dementias, 30(7), 672-678. doi:10.1177/1533317512461555