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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 7758406)

  • 1. Human subject issues in drug abuse research. College on Problems of Drug Dependence.
    Adler MW
    Drug Alcohol Depend; 1995 Feb; 37(2):167-75. PubMed ID: 7758406
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ethical issues in clinical neurological research.
    Shore D; Berg K; Mullican C
    J Calif Alliance Ment Ill; 1994; 5(1):61-2. PubMed ID: 11653329
    [No Abstract]   [Full Text] [Related]  

  • 3. The IRB's role in assessing the generalizability of non-NIH-funded clinical trials.
    Weijer C
    IRB; 1998; 20(2-3):1-5. PubMed ID: 11656912
    [No Abstract]   [Full Text] [Related]  

  • 4. College on Problems of Drug Dependence Policy on Administering Drugs with Abuse Potential in Human Research.
    Drug Alcohol Depend; 1996 Dec; 43(1-2):115-7. PubMed ID: 8957150
    [No Abstract]   [Full Text] [Related]  

  • 5. Continuing review of research involving human subjects: approach to the problem and remaining areas of concern.
    Gordon B; Prentice E
    IRB; 1997; 19(2):8-11. PubMed ID: 11655323
    [No Abstract]   [Full Text] [Related]  

  • 6. The paradoxical case of payment as benefit to research subjects.
    Macklin R
    IRB; 1989; 11(6):1-3. PubMed ID: 11650284
    [No Abstract]   [Full Text] [Related]  

  • 7. The changing clinical trials scene: the role of the IRB.
    Mitchell SC; Steingrub J
    IRB; 1988; 10(4):1-5. PubMed ID: 11650078
    [No Abstract]   [Full Text] [Related]  

  • 8. Proposal on waiver of informed consent poses major issues for research ethics.
    Maloney DM
    Hum Res Rep; 1997 Sep; 12(9):1-3. PubMed ID: 11660533
    [No Abstract]   [Full Text] [Related]  

  • 9. Considering experimentation and elusive truth: informed consent made difficult.
    Brodeur D
    Issues (St Louis Mo); 1992; 7(2):1-8. PubMed ID: 11659444
    [No Abstract]   [Full Text] [Related]  

  • 10. IRB review of adverse events in investigational drug studies.
    Prentice ED; Gordon B
    IRB; 1997; 19(6):1-4. PubMed ID: 11656910
    [No Abstract]   [Full Text] [Related]  

  • 11. College on Problems of Drug Dependence policy on administering drugs with abuse potential in human research.
    College on Problems of Drug Dependence
    IRB; 1996; 18(5):5-7. PubMed ID: 11654740
    [No Abstract]   [Full Text] [Related]  

  • 12. Issues related to the protection of human research participants.
    Harrison L
    J Neurosurg Nurs; 1993 Jun; 25(3):187-93. PubMed ID: 11660053
    [No Abstract]   [Full Text] [Related]  

  • 13. "Evaluation of human subject protections in schizophrenia research conducted by the University of ..." (Part III).
    Maloney DM
    Hum Res Rep; 2000 Jan; 15(1):5-6. PubMed ID: 11658036
    [No Abstract]   [Full Text] [Related]  

  • 14. An IRB member's perspective on access to innovative therapy.
    Moore DL
    Albany Law Rev; 1994; 57(3):559-81. PubMed ID: 11652854
    [No Abstract]   [Full Text] [Related]  

  • 15. FDA's new rule on treatment use and sale of investigational new drugs.
    Levine RJ
    IRB; 1987; 9(4):1-4. PubMed ID: 11649946
    [No Abstract]   [Full Text] [Related]  

  • 16. Ethical and legal considerations in dental caries research involving human subjects.
    Branson R
    J Dent Res; 1980 Jul; 59(Special Issue C):1214-364. PubMed ID: 11651755
    [No Abstract]   [Full Text] [Related]  

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

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

  • 19. Institutional review boards in the university setting: review of pharmaceutical testing protocols, informed consent and ethical concerns.
    Kobasic DM
    J Coll Univ Law; 1988; 15(2):185-216. PubMed ID: 11659168
    [No Abstract]   [Full Text] [Related]  

  • 20. IRBs and randomized clinical trials.
    Meinert CL
    IRB; 1998; 20(2-3):9-12. PubMed ID: 11656915
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.