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Journal Abstract Search
404 related items for PubMed ID: 11653322
1. The ethics of research in mental illness. Ghaemi SN, Hundert EM. J Calif Alliance Ment Ill; 1994; 5(1):47-9. PubMed ID: 11653322 [No Abstract] [Full Text] [Related]
2. A relational perspective on ethics-in-science decisionmaking for research with vulnerable populations. Fisher CB. IRB; 1997; 19(5):1-4. PubMed ID: 11655184 [No Abstract] [Full Text] [Related]
3. Autonomy, beneficence, and the experimental subject's consent: a response to Jay Katz. Pellegrino ED. St Louis Univ Law J; 1993; 38(1):55-62. PubMed ID: 11656324 [No Abstract] [Full Text] [Related]
4. Balancing moral principles in federal regulations on human research. Ackerman TF. IRB; 1992; 14(1):1-6. PubMed ID: 11652041 [No Abstract] [Full Text] [Related]
5. Human experimentation and human rights. Katz J. St Louis Univ Law J; 1993; 38(1):7-54. PubMed ID: 11656326 [No Abstract] [Full Text] [Related]
6. Institutional review boards and research on individuals with mental disorders. Hoppe SK. Account Res; 1996; 4(3-4):187-95. PubMed ID: 11654514 [No Abstract] [Full Text] [Related]
7. An overview of legal controls on human experimentation and the regulatory implications of taking Professor Katz seriously. Goldner JA. St Louis Univ Law J; 1993; 38(1):63-134. PubMed ID: 11656325 [No Abstract] [Full Text] [Related]
9. Informed consent in human experimentation: bridging the gap between ethical thought and current practice. Delgado R, Leskovac H. UCLA Law Rev; 1986 Oct; 34(1):67-130. PubMed ID: 11659049 [No Abstract] [Full Text] [Related]
10. Ethical standards for human subject research in developing countries. Miller J, Crigger BJ. IRB; 1992 Oct; 14(3):7-8. PubMed ID: 11656138 [No Abstract] [Full Text] [Related]
11. A communal model for presumed consent for research on the neurologically vulnerable. Thomasma DC. Account Res; 1996 Oct; 4(3-4):227-39. PubMed ID: 11654518 [No Abstract] [Full Text] [Related]
12. Standards of accountability for consent in research. Rubenstein LS. Account Res; 1996 Oct; 4(3-4):197-206. PubMed ID: 11654515 [No Abstract] [Full Text] [Related]
14. Issues presented by mandatory reporting requirements to researchers of child abuse and neglect. Sieber JE. Ethics Behav; 1994 Oct; 4(1):1-22. PubMed ID: 11652712 [Abstract] [Full Text] [Related]
15. Obtaining consent for research in the neurobiologically impaired. Thomasma DC. J Calif Alliance Ment Ill; 1994 Oct; 5(1):54-5. PubMed ID: 11653324 [No Abstract] [Full Text] [Related]
16. Integrating science and ethics in research with high-risk children and youth. Fisher CB. Soc Policy Rep; 1993 Oct; 7(4):1-27. PubMed ID: 11659850 [No Abstract] [Full Text] [Related]
17. Decisional capacity, older human research subjects, and IRBs: beyond forms and guidelines. Kapp MB. Stanford Law Pol Rev; 1998 Oct; 9(2):359-71. PubMed ID: 11657514 [No Abstract] [Full Text] [Related]
18. Bioethics group divided over research on mentally ill. Weiss R. Washington Post; 1998 Nov 16; ():A6. PubMed ID: 11648074 [No Abstract] [Full Text] [Related]
19. The regulation of human experimentation in the United States--a personal odyssey. Katz J. IRB; 1987 Nov 16; 9(1):1-6. PubMed ID: 11649890 [No Abstract] [Full Text] [Related]
20. Building a new consensus: ethical principles and policies for clinical research on HIV/AIDS. Levine C, Dubler NN, Levine RJ. IRB; 1991 Nov 16; 13(1-2):1-17. PubMed ID: 11659323 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]