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  1. Balancing Privacy Protections with Efficient Research: Institutional Review Boards and the Use of Certificates of Confidentiality.Peter M. Currie - 2005 - IRB: Ethics & Human Research 27 (5):7.
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  2. Confidentiality: More Than a Linkage File and a Locked Drawer.Michele M. Easter, Arlene M. Davis & Gail E. Henderson - 2004 - IRB: Ethics & Human Research 26 (2):13.
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  3. Correction and Clarification: Therapeutic Misconception in Clinical Research: Frequency and Risk Factors.Paul S. Appelbaum, Charles W. Lidz & Thomas Grisso - 2004 - IRB: Ethics & Human Research 26 (5):18.
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  4. Costs to Subjects for Research Participation and the Informed Consent Process: Regulatory and Ethical Considerations.Ana S. Iltis - 2004 - IRB: Ethics & Human Research 26 (6):9.
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  5. The Subject Advocate: Protecting the Interests of Participants with Fluctuating Decisionmaking Capacity.Scott Stroup & Paul Appelbaum - 2003 - IRB: Ethics & Human Research 25 (3):9.
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  6. Attending to Local Justice: Lessons From Pediatric HIV.Holly A. Taylor & Nancy E. Kass - 2002 - IRB: Ethics & Human Research 24 (6):9.
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  7. Ethical Issues in Including Suicidal Individuals in Clinical Research.Celia B. Fisher, Jane L. Pearson, Scott Kim & Charles F. Reynolds - 2002 - IRB: Ethics & Human Research 24 (5):9.
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  8. The Right of Subjects to See the Protocol.Robert M. Veatch - 2002 - IRB: Ethics & Human Research 24 (5):6.
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  9. Pilot Study: Does the White Coat Influence Research Participation?Jon F. Merz, Timothy R. Rebbeck, Pamela Sankar & Emma A. Meagher - 2002 - IRB: Ethics & Human Research 24 (4):6.
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  10. Enough Is Enough?: Disclosure in Cross-Cultural Research.C. Cox Macpherson & R. L. Connolly - 2002 - IRB: Ethics & Human Research 24 (3):7.
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  11. When IRBs Disagree: Waiving Parental Consent for Sexual Health Research on Adolescents.Mark Risjord & Judith Greenberg - 2002 - IRB: Ethics & Human Research 24 (2):8.
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  12. Full Disclosure for Open Label Studies.Greg Nycz & Grace Nycz - 2001 - IRB: Ethics & Human Research 23 (6):15.
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  13. Eligibility, Extrapolation & Equipoise: Unlearned Lessons in the Ethical Analysis of Clinical Research.Robert A. Crouch - 2001 - IRB: Ethics & Human Research 23 (4):6.
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  14. Protocol 126 and "The Hutch".Robert M. Nelson - 2001 - IRB: Ethics & Human Research 23 (3):14.
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  15. Children as Research Subjects: New Guidelines for Canadian IRBs.David C. Flagel - 2000 - IRB: Ethics & Human Research 22 (5):1.
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  16. Moral Problems in Assessing Research Risk.Loretta M. Kopelman - 2000 - IRB: Ethics & Human Research 22 (5):3.
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  17. Moral Solutions in Assessing Research Risk.Paul B. Miller & Charles Weijer - 2000 - IRB: Ethics & Human Research 22 (5):6.
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  18. Practicing Safer Research Using the Law to Protect the Confidentiality of Sensitive Research Data.Leslie E. Wolf & Bernard Lo - 1999 - IRB: Ethics & Human Research 21 (5):4.
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  19. Regulatory Orphans: Juvenile Prisoners as Transvulnerable Research Subjects.Joyce G. Reed - 1999 - IRB: Ethics & Human Research 21 (2):9.
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  20. The Noninstitutional Review Board: What Distinguishes Us From Them?Erica Heath - 1998 - IRB: Ethics & Human Research 20 (5):8.
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  21. What Patients Say About Medical Research.Jeremy Sugarman, Nancy E. Kass, Steven N. Goodman, Patricia Perentesis, Praveen Fernandes & Ruth R. Faden - 1998 - IRB: Ethics & Human Research 20 (4):1.
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  22. Continuing IRB Review When Research Activity Is Limited to Routine Follow-Up Evaluations.Robert J. Amdur & Elizabeth Bankert - 1997 - IRB: Ethics & Human Research 19 (1):7.
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  23. Psychology Faculty Satisfaction and Compliance with IRB Procedures.Becky J. Liddle & Elizabeth W. Brazelton - 1996 - IRB: Ethics & Human Research 18 (6):4.
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  24. Educating Subjects About the IRB's Role.Lynn Meyer - 1996 - IRB: Ethics & Human Research 18 (6):8.
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  25. The Use of Normal Children as Participants in Research on Therapy.Bruce Gordon, Ernest Prentice & Paul Reitemeier - 1996 - IRB: Ethics & Human Research 18 (3):5.
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  26. The NIH Inclusion Guidelines: Challenges for the Future.Karen H. Rothenberg, Eugene G. Hayunga, Joyce E. Rudick & Vivian W. Pinn - 1996 - IRB: Ethics & Human Research 18 (3):1.
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  27. Who Understands? II: A Survey of 27 Words, Phrases, or Symbols Used in Proposed Clinical Research Consent Forms.William C. Waggoner & Barbara B. Sherman - 1996 - IRB: Ethics & Human Research 18 (3):8.
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  28. Exempt Research: Procedures in the Intramural Research Program of the National Institutes of Health.Alison Wichman, Deloris Mills & Alan L. Sandler - 1996 - IRB: Ethics & Human Research 18 (2):3.
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  29. Drug-Free Research in Schizophrenia: An Overview of the Controversy.Paul S. Appelbaum - 1996 - IRB: Ethics & Human Research 18 (1):1.
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  30. The IRB, Ethics, and the Objective Study of Religion in Health.Stephen G. Post - 1995 - IRB: Ethics & Human Research 17 (5/6):8.
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  31. Who Understands? A Survey of 25 Words or Phrases Commonly Used in Proposed Clinical Research Consent Forms.William C. Waggoner & Diane M. Mayo - 1995 - IRB: Ethics & Human Research 17 (1):6.
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  32. Asking the Sensitive Question: The Ethics of Survey Research and Teen Sex.Sarah R. Phillips - 1994 - IRB: Ethics & Human Research 16 (6):1.
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  33. Research with Radiation and Healthy Children: Greater Than Minimal Risk.William L. Freeman - 1994 - IRB: Ethics & Human Research 16 (5):1.
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  34. Does Radiation Research in Healthy Children Pose Greater Than Minimal Risk?Bonnie L. Specker & Eugene L. Saenger - 1994 - IRB: Ethics & Human Research 16 (5):5.
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  35. An Update on the PEG-SOD Study Involving Incompetent Subjects: FDA Permits an Exception to Informed Consent Requirements.Ernest D. Prentice, L. Antonson, Lyal G. Leibrock, Vikram C. Prabhu, Timothy K. Kelso & Thomas D. Sears - 1994 - IRB: Ethics & Human Research 16 (1/2):16.
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  36. Participation in Pedigree Studies and the Risk of Impeded Access to Health Insurance.Nancy E. Kass - 1993 - IRB: Ethics & Human Research 15 (5):7.
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  37. Ethical, Legal, and Political Problems Affecting Epidemiology in European Countries.Claes-Göran Westrin - 1993 - IRB: Ethics & Human Research 15 (3):6.
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  38. Research Ethics in Applied Anthropology.Patricia A. Marshall - 1992 - IRB: Ethics & Human Research 14 (6):1.
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  39. Community Consultation and AIDS Clinical Trials: Part III.Herbert R. Spiers - 1991 - IRB: Ethics & Human Research 13 (5):3.
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  40. Behavioral Research Involving Children: A Developmental Perspective on Risk.Ross A. Thompson - 1990 - IRB: Ethics & Human Research 12 (2):1.
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  41. FDA Issues Concerning Conflicts of Interest.Thomas L. Kurt - 1990 - IRB: Ethics & Human Research 12 (5):6.
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  42. Protectionism and the New Research Imperative in Pediatric AIDS.Terrence F. Ackerman - 1990 - IRB: Ethics & Human Research 12 (5):1.
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  43. A Pilot Project: Bioethics Consultants as Non-Voting Members of IRBs at the National Institutes of Health.Evan G. DeRenzo & Alison Wichman - 1990 - IRB: Ethics & Human Research 12 (6):6.
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  44. Sharing Scientific Data III: Planning and the Research Proposal.Nancy Flournoy & Leonard B. Hearne - 1990 - IRB: Ethics & Human Research 12 (3):6.
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  45. Changes in the Office for Protection From Research Risks.Charles R. McCarthy - 1990 - IRB: Ethics & Human Research 12 (2):11.
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  46. Cohort-Specific Consent: An Honest Approach to Phase 1 Clinical Cancer Studies.Benjamin Freedman - 1990 - IRB: Ethics & Human Research 12 (1):5.
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  47. Bioethics Consultants' Roles on IRBs.Bioethics Consultant Group - 1990 - IRB: Ethics & Human Research 12 (6):11.
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  48. Research Fraud, Misconduct, and the IRB.Stephen Hilgartner - 1990 - IRB: Ethics & Human Research 12 (1):1.
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  49. Protecting Human Subjects From Harm Through Improved Risk Judgments.Eric M. Meslin - 1990 - IRB: Ethics & Human Research 12 (1):7.
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  50. On Studying the Powerful (Or Fearing to Do So): A Vital Role for IRBs.Joan E. Sieber - 1989 - IRB: Ethics & Human Research 11 (5):1.
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