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Noelker, L. S., & Whitlatch, C. J. (2000). Informal caregiving. In G. L. Maddox (Ed.), The encyclopedia of aging, third edition (pp. 541-544). New York, NY: Springer.

Anetzberger, G. J. Ejaz, F. K., Bukach, A., Bass, D. (2014). Next steps: Documentation and accessing community healthcare resources. In R. M. Factora (Ed.), Aging and money: Reducing risk of financial exploitation and protecting financial resources (pp. 79-90). New York, NY: Springer.

Pinciotti, C. M., Bass, D. M., McCarthy, C. A., Judge, K. S., Wilson, N. L., Morgan, R. O., Snow, A. L., & Kunik, M. E. (2016). Negative consequences of family caregiving for veterans with PTSD and dementia. The Journal of Nervous and Mental Disease, 0(0), 1-6. doi:10.1097/NMD.0000000000000560

Bass, D. M., Judge, K. S., Snow, A. L., Wilson, N. L., Looman, W. J., McCarthy, K., Morgan, R., Abloorh-Odjidja, C., & Kunik, M. E. (2012). Negative caregiving effects among caregivers of veterans with dementia. The American Journal of Geriatric Psychiatry, 20(3), 239-247. doi:10.1097/JGP.0b013e31824108ca

Whitlatch, C. J., & Orsulic-Jeras, S. (2018). Meeting the informational, educational, and psychosocial support needs of persons living with dementia and their family caregivers. Gerontologist, 58(S1), S58-S73. doi:10.1093/geront/gnx162