Informed Consent and Clinical Trial Participation: Perspectives from a Ghanaian Community
Author:
Publisher
Palgrave Macmillan US
Link
http://link.springer.com/content/pdf/10.1057/9781137456038_2
Reference70 articles.
1. Angell, M. 1997. “The Ethics of Clinical Research in the Third World.” The New England Journal of Medicine 337 (12): 847–849.
2. Appelbaum, P. S., M. Anatchkova, K. Albert, L. B. Dunn, and C. W. Lidz. 2012. “Therapeutic Misconception in Research Subjects: Development and Validation of a Measure.” Clinical Trials (London, England) 9(6): 748–61. Accessed July 7, 2013. http://www.ncbi.nlm.nih.gov /pubmed/22942217.
3. Appelbaum, P. S., L. H. Roth, and C. Lidz. 1982. “The Therapeutic Misconception: Informed Consent in Psychiatric Research.” International Journal of Law and Psychiatry 5(3–4): 319–29. Accessed July 7, 2013. http://www.ncbi.nlm.nih.gov /pubmed/6135666.
4. Appelbaum, P. S., L. H. Roth, C. W. Lidz, P. Benson, and W. Winslade. 1987. “False Hopes and Best Data: Consent to Research and the Therapeutic Misconception.” Hastings Center Report 2: 20–24.
5. Ballantyne, A. J. 2010. “How to Do Research Fairly in an Unjust World.” The American Journal of Bioethics: 10(6): 26–35. Accessed July 7, 2013. http://www.ncbi. nlm.nih.gov/pubmed/20526966.
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