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PUBMED FOR HANDHELDS

Journal Abstract Search


625 related items for PubMed ID: 11660533

  • 61. Regulatory orphans: juvenile prisoners as transvulnerable research subjects.
    Reed JG.
    IRB; 1999; 21(2):9-14. PubMed ID: 11657875
    [No Abstract] [Full Text] [Related]

  • 62. The politics of informed consent.
    Weston HB.
    Natl Forum; 1978; 58(4):23-6. PubMed ID: 11661867
    [No Abstract] [Full Text] [Related]

  • 63. FDA seeks public comment on informed consent rules in combat situations.
    Hastings Cent Rep; 1997; 27(5):43. PubMed ID: 11645003
    [No Abstract] [Full Text] [Related]

  • 64. Constraints on experimentation: protecting children to death.
    Holder AR.
    Yale Law Policy Rev; 1988; 6(1):137-56. PubMed ID: 11650241
    [No Abstract] [Full Text] [Related]

  • 65. IRBs and research with human biological materials.
    Maloney DM.
    Hum Res Rep; 1999 Jan; 14(1):2. PubMed ID: 11657556
    [No Abstract] [Full Text] [Related]

  • 66. Informed consent to participate in research: Part II.
    Levine RJ.
    Bioethics Dig; 1977 Apr; 1(12):1-16. PubMed ID: 11664810
    [No Abstract] [Full Text] [Related]

  • 67. Non-therapeutic medical research involving human subjects.
    Bloom MJ.
    Syracuse Law Rev; 1973 Apr; 24():1067-1099. PubMed ID: 11664224
    [No Abstract] [Full Text] [Related]

  • 68. Institutional review boards and public health research: an analysis.
    Hogue LL.
    Univ Ark Little Rock Law J; 1978 Apr; 1(2):428-54. PubMed ID: 11661619
    [No Abstract] [Full Text] [Related]

  • 69. A look at the bioresearch monitoring program: the agency perspective.
    Brisson EL.
    Food Drug Cosmet Law J; 1983 Apr; 38(2):184-9. PubMed ID: 11649578
    [No Abstract] [Full Text] [Related]

  • 70. Multicenter trials and subject eligibility: should local IRBs play a role?
    Freedman B.
    IRB; 1994 Apr; 16(1-2):1-6. PubMed ID: 11652320
    [No Abstract] [Full Text] [Related]

  • 71. Are clinical trials of cell transplantation for Duchenne muscular dystrophy ethical?
    Cho MK.
    IRB; 1994 Apr; 16(1-2):12-5. PubMed ID: 11652321
    [No Abstract] [Full Text] [Related]

  • 72. Using the brain dead for medical research.
    Martyn SR.
    Utah Law Rev; 1986 Apr; 1986(1):1-28. PubMed ID: 11651917
    [No Abstract] [Full Text] [Related]

  • 73. Research involving children: an interpretation of the new regulations.
    Levine RJ.
    IRB; 1983 Apr; 5(4):1-5. PubMed ID: 11649521
    [No Abstract] [Full Text] [Related]

  • 74. If a subject incurs obligations and carries them out, then consent is a contract: Dahl v. HEM Pharmaceuticals (Part II).
    Maloney DM.
    Hum Res Rep; 1996 Jan; 11(1):4-5. PubMed ID: 11653221
    [No Abstract] [Full Text] [Related]

  • 75. IRB review of a Phase II randomized clinical trial involving incompetent patients suffering from severe closed head injury.
    Prentice ED, Antonson DL, Leibrock LG, Kelso TK, Sears TD.
    IRB; 1993 Jan; 15(5):1-7. PubMed ID: 11659703
    [No Abstract] [Full Text] [Related]

  • 76. Human experimentation: the review process in practice.
    Cowan DH.
    Case West Reserve Law Rev; 1975 Jan; 25(3):533-64. PubMed ID: 11661165
    [No Abstract] [Full Text] [Related]

  • 77. Power, advocacy, and informed consent forms.
    Smith ML.
    J Calif Alliance Ment Ill; 1994 Jan; 5(1):25-7. PubMed ID: 11653311
    [No Abstract] [Full Text] [Related]

  • 78.
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  • 79.
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  • 80.
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