These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


416 related items for PubMed ID: 11657514

  • 1. Decisional capacity, older human research subjects, and IRBs: beyond forms and guidelines.
    Kapp MB.
    Stanford Law Pol Rev; 1998; 9(2):359-71. PubMed ID: 11657514
    [No Abstract] [Full Text] [Related]

  • 2. A communal model for presumed consent for research on the neurologically vulnerable.
    Thomasma DC.
    Account Res; 1996; 4(3-4):227-39. PubMed ID: 11654518
    [No Abstract] [Full Text] [Related]

  • 3. Proposed guidelines for the participation of persons with dementia as research subjects.
    Keyserlingk EW, Glass K, Kogan S, Gauthier S.
    Perspect Biol Med; 1995; 38(2):319-61. PubMed ID: 11644666
    [No Abstract] [Full Text] [Related]

  • 4. Guidelines for addressing ethical and legal issues in Alzheimer disease research: a position paper.
    High DM, Whitehouse PJ, Post SG, Berg L.
    Alzheimer Dis Assoc Disord; 1994; 8(Suppl. 4):66-74. PubMed ID: 11657676
    [No Abstract] [Full Text] [Related]

  • 5. 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]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Why the tolerance of potential harms? Research ethics in Alzheimer disease.
    Post SG.
    Account Res; 1999; 7(2-4):241-53. PubMed ID: 11658179
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Ethical standards for human subject research in developing countries.
    Miller J, Crigger BJ.
    IRB; 1992; 14(3):7-8. PubMed ID: 11656138
    [No Abstract] [Full Text] [Related]

  • 13. Minors' assent, consent, or dissent to medical research.
    Leikin S.
    IRB; 1993; 15(2):1-7. PubMed ID: 11651566
    [No Abstract] [Full Text] [Related]

  • 14. Proxy decision making in Alzheimer disease research: durable powers of attorney, guardianship, and other alternatives.
    Kapp MB.
    Alzheimer Dis Assoc Disord; 1994; 8(Suppl. 4):28-37. PubMed ID: 11657671
    [Abstract] [Full Text] [Related]

  • 15. IRBs: protecting the well-being of subject-participants with mental disorders that may affect decisionmaking capacity.
    Baylis F.
    Account Res; 1999; 7(2-4):183-99. PubMed ID: 11658175
    [No Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. 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]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. The new Dutch 'medical experimentation bill' and incompetent patients.
    Cusveller BS, Jochemsen H.
    Ethics Med; 1993; 9(2):18-20. PubMed ID: 11652740
    [No Abstract] [Full Text] [Related]

  • 20. Obtaining consent for research in the neurobiologically impaired.
    Thomasma DC.
    J Calif Alliance Ment Ill; 1994; 5(1):54-5. PubMed ID: 11653324
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 21.