The SRA Symposium - College of Medicine

Papers
Potts, A., Grace, V., Gavey, N., and Vares, T. (2004). Viagra Stories: Challenging ‘Erectile Dysfunction’.
Social Science and Medicine 59: 489-499.
Pullman, D. (2002). Conflicting Interests, Social Justice and Proxy Consent to Research. Journal of
Medicine and Philosophy 27(5): 523-545.
Sankar, P. (2004). Communication and Miscommunication in Informed Consent to Research.
Medical Anthropology Quarterly 18(4): 429-446.
Schron, E.B., Wassertheil-Smoller, S., and Pressel, S. (1997). Clinical Trial Participant Satisfaction:
Survey of SHEP Enrollees. Journal of the American Geriatrics Society 45(8): 1772-1777.
Sharp, L.A. (2000). The Commodification of the Body and Its Parts. Annual Review of Anthropology
29: 287-328.
Siminoff, L.A. (2003). Toward Improving the Informed Consent Process in Research with Humans.
IRB: Ethics and Human Research 25(5): S1-S3.
Smyth, W.E., and Murray, M.J. (2000). Owning the Story: Ethical Considerations in Narrative
Research. Ethics & Behavior 10(4): 311-336.
Sugarman, J., McCrory, D.C., Powell, D., Krasny, A., Adams, B., Ball, E., and Casell, C. (1999). Empirical
Research on Informed Consent: An Annotated Bibliography. Hastings Center Report
29(1):S1-S42.
Ten Have, H. (1994). Principlism: A Western European Appraisal. In E.R. DuBose, R.P. Hamel,
and L.J. O’Connell (Eds.), A Matter of Principles? Ferment in U.S. Bioethics (pp. 101-120).
Valley Forge, PA: Trinity Press International.
Vanderpool, H.Y., and Weiss, G.B. (1987). False Data and Last Hopes: Enrolling Ineligible Patients
in Clinical Trials. Hastings Center Report 17(2): 16-19.
Wolf, S.M. (1996). Introduction: Gender and Feminism in Bioethics. In S.M. Wolf (Ed.), Feminism
and Bioethics: Beyond Reproduction (pp. 3-43). New York: Oxford University Press.
34 2005 Symposium Proceedings Book