Becker, T.D., Lin, H.C. & Miller, V.A. (2018). A patient study of observed physician-parent-child communication and child satisfaction in a gastroenterology clinic. Patient Preference and Adherence, 12, 1327-1335.
Boeka, A. G., Solomon, A. C., Lokken, K., McGuire, B. M., & Bynon, J. S. (2011). A biopsychosocial approach to liver transplant evaluation in two patients with Wilson's disease. Psychology, Health & Medicine, 16(3), 268–275.
Bosma, H., Johnston, M., Cadell, S., Wainwright, W., Abernethy, N., Feron, A., … Nelson, F. (2010). Creating social work competencies for practice in hospice palliative care. Palliative Medicine, 24(1), 79–87.
Chiang, J.J., Miller, G. E., Turiano, N.A., Mroczek, D.K. (2018). Affective reactivity to daily stress and 20-year mortality risk in adults with chronic illness: Findings from the national study of daily experiences. Health Psychology, 37(2), 170-178.
Coleman, S. M., Katon, W., Lin, E., & Von Korff, M. (2013). Depression and death in diabetes; 10-year follow-up of all- cause and cause-specific mortality in a diabetic cohort. Psychosomatics, 54(5), 428–436.
Crouch, E., Strompolis, M., Radcliff, E., Srivastav, A. (2018). Examining exposure to adverse childhood experiences and later outcomes of poor physical and mental health among South Carolina adults. Children and Youth Services Review, 84, 193-197.
Empeno, J., Raming, N. T. J., Irwin, S. A., Nelesen, R. A., & Lloyd, L. S. (2011). The hospice caregiver support project: Providing support to reduce caregiver stress. Journal of Palliative Medicine, 14(5), 593–597.
Ghoshal, A., Salins, N., Damani, A., Deodhar, J. & Muckaden, M. (2016). Specialist pediatric palliative care referral practices in pediatric oncology: A large 5-year retrospective audit. Indian Journal of Palliative Care 22(3), 266-273.
Goldberg, A., & Rickler, K. S. (2011). The role of family caregivers for people with chronic illness. Medicine and Health, Rhode Island, 94(2), 41–42. Retrieved from http://www.rimed.org/medhealthri/2011-02/2011-02- 41.pdf
Greene, G. M. (2013). Description of a psychosocial assessment instrument and risk criteria to support social work recommendations for kidney transplant candidates. Social Work in Health Care, 52(4), 370–396.
Hoy-Ellis, C.P., Fredriksen-Goldsen, K.I. (2016). Lesbian, gay & bisexual older adults: Linking internal minority stressors, chronic health conditions and depression. Aging and Mental Health, 20(11), 1119-1130.
Kent, E. E., Parry, C., Montoya, M. J., Sender, L. S., Morris, R. A., & Anton-Culver, H. (2012). "You're too young for this": Adolescent and young adults' perspectives on cancer survivorship. Journal of Psychosocial Oncology, 30(2), 260– 279.
Lai, C., Luciani, M., Morelli, E., Galli, F., Cappelluti, R., … Lombardo, L. (2013). Predictive role of different dimensions of burden for risk of complicated grief in caregivers of terminally ill patients. American Journal of Hospice & Palliative Care [Epub ahead of print].
Lanier, P., Bollinger, S., & Krueger, R. F. (2013). Advances in the conceptualization of personality disorders: Issues affecting social work practice and research. Clinical Social Work Journal, 41(2), 155–162.
Lee, A.A., Piette, J.D., Heisler, M., Janevic, M.R. Langa, K.M.& Rosland, A-M. (2017). Family members’ experiences supporting adults with chronic illness: A national survey. Families, Systems, & Health, 35(4), 463-473.
Mutchler, M. G., Wagner, G., Cowgill, B. O., McKay, T., Risley, B., & Bogart, L. M. (2011). Improving HIV/AIDS care through treatment advocacy: Going beyond client education to empowerment by facilitating client–provider relationships. AIDS Care, 23(1), 79–90.
Northhouse, L. L., Katapodi, M. C., Schafenacker, A. M., & Weiss, D. (2012). The impact of caregiving on the psychological well-being of family caregivers and cancer patients. Seminars in Oncology Nursing, 28(4), 236–245.
O’Connor, M., & Fisher, C. (2011). Exploring the dynamics of interdisciplinary palliative care teams in providing psychosocial care: “Everybody thinks that everybody can do it and they can't.” Journal of Palliative Medicine, 14(2), 191–196.
Sarwer, D. B., & Dilks, R. J. (2012). Invited commentary: Childhood and adolescent obesity: Psychological and behavioral issues in weight loss treatment. Journal of Youth & Adolescence, 41(1), 98–104.
Tischler, S., Webster, M., Wittmann, D., & Wade, K. (2017). Developing and sustaining a practice-based research infrastructure in a hospital social work department: Why is it important? Social Work in Health Care, 56(1), 1-12.
Uchino, B. N. (2009). Understanding the links between social support and physical health: A life-span perspective with emphasis on the separability of perceived and received support. Perspectives on Psychological Science, 4(3), 236–255.
Uchino, B. N., Bowen, K., Carlisle, M., & Birmingham, W. (2012). Psychological pathways linking social support to health outcomes: A visit with the "ghosts" of research past, present, and future. Social Science and Medicine, 74(7), 949–957.
Zavagli, V., Miglietta, E., Varani, S., Pannuti, R., Brighetti, G. & Pannuti, F. (2016). Associations between caregiving worries and psychophysicial well-being. An investigation on home- cared cancer patients family caregivers. Supportive Care in Cancer, 24(2), 857-863.
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