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The following HTML text is provided to enhance online readability. Many aspects of typography translate only awkwardly to HTML. Please use the page image as the authoritative form to ensure accuracy. Ratzan, R. 1985 Technical aspects of obtaining informed consent from persons with senile dementia of the Alzheimer type. In Alzheimer’s Dementia: Dilemmas in Clinical Research, V. Melnick and N. Dubler, eds. Clifton, NJ: Humana Press. Runyan, D. 1999 Maltreatment in families: A research dilemma. In Beyond Regulations, N. King, G. Henderson, and J. Stein, eds. Chapel Hill: University of North Carolina Press. 2000 The ethical, legal, and methodological implications of directly asking children about abuse. Journal of Interpersonal Violence 15:675–681. Sachs, G., and C. Cassel 1990 Biomedical research involving older human subjects. Law, Medicine & Health Care 18:234–243. Sachs, G., J. Rhymes, and C. Cassel 1993 Biomedical and behavioral research in nursing homes: Guidelines for ethical investigations. Journal of the American Geriatrics Society 41:771–777. U.S. Department of Health and Human Services 1981 Final Regulations Amending Basic HHS Policy for the Protection of Human Subjects. Federal Register 46:8366–8391. 1991 Federal Policy for the Protection of Human Subjects (Common Rule). Federal Register 56:28,012–28,018. 1999 Additional Protections for Children Involved as Subjects in Research, Code of Federal Regulations 45:§ 46.408(c). U.S. Food and Drug Administration 1999 Protection of Human Subjects. Code of Federal Regulations 21: Parts 50 and 56. Wendler, D., and K. Prasad 2001 Core safeguards for clinical research with adults who are unable to consent. Annals of Internal Medicine 135:514–523. World Medical Association 2000 Declaration of Helsinki: Ethical principles for medical research involving human subjects. Journal of the American Medical Association 284:3043–3045.
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