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 | Volume 6 Number 6 | November-December 2006
 Table of Contents
Disclosing Individual Genetic Results to Research Participants
by Vardit Ravitsky
Analogical Reasoning in Handling Emerging Technologies: The Case of Umbilical Cord Blood Biobanking
by Bjorn Hofmann, Soren Holm, Jan Helge Solbakk
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 | Volume 6 Number 5 | September-October 2006
Table of Contents
Damage Compounded: Disparities, Distrust, and Disparate Impact in End-of-Life Conflict Resolution Policies
by Mary Ellen Wojtasiewicz
Altruistic Discourse in the Informed Consent Process for Childhood Cancer Clinical Trials
by Christian Simon, Michelle Eder, Eric Kodish, Laura A. Siminoff
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 | Volume 6 Number 4 | July-August 2006
Table of Contents
Ethics and Professionalism: What Does a Resident Need to Learn?
by Susan Door Goold
The Real Problem with Equipoise
by Winston Chiong
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 | Volume 6 Number 3 | May-June 2006
Table of Contents
Accidental Communities: Race, Emergency Medicine, and the Problem of PolyHeme
by Karla F.C. Holloway
An Open Letter to Institutional Review Boards Considering Northfield Laboratories' PolyHeme Trial
by Kenneth Kipnis, Nancy M.P. King, Robert M. Nelson
Against Bioethics: A Decision Analysis of Consent
by Jonathan Baron
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 | Volume 6 Number 2 | March-April 2006
Table of Contents
A Defense of Unqualified Medical Confidentiality
by Kenneth Kipnis
Rural Health Care Ethics: Is There a Literature?
by William Nelson, Gili Lushkov, Andrew Pomerantz, William B. Weeks
Toward a Reconstruction of Medical Morality
by Edmund D. Pellegrino
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 | Volume 6 Number 1 | January-February 2006
Table of Contents
Informed Consent Revisited: Japan and the U.S.
by Akira Akabayashi, Brian Taylor Slingsby
The Doctor-Patient Relationship in the Post-Managed Care Era
by G. Caleb Alexander, John Lantos
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