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Profile: Rob de Vries (University of Amsterdam)
Profile: Robert Hans de Vries (Universiteit van Amsterdam)
  1.  7
    Raymond de Vries & Jill A. Fisher (2013). Introduction. Cambridge Quarterly of Healthcare Ethics 22 (4):389-390.
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  2.  18
    Raymond Vries (2004). How Can We Help? From "Sociology in" to "Sociology of" Bioethics. Journal of Law, Medicine & Ethics 32 (2):279-292.
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  3.  1
    M. Constantine, M. Allyse, M. Wall, R. D. Vries & T. Rockwood (2014). Imperfect Informed Consent for Prenatal Screening: Lessons From the Quad Screen. Clinical Ethics 9 (1):17-27.
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  4.  7
    S. Y. Kim, R. Vries, R. Wilson, S. Parnami, S. Frank, K. Kieburtz & R. G. Holloway (2012). Research Participants' "Irrational" Expectations: Common or Commonly Mismeasured? IRB: Ethics & Human Research 35 (1):1-9.
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  5. R. Vries (2006). Ethical Concepts Regarding the Genetic Engineering of Laboratory Animals. Medicine, Health Care and Philosophy 9 (2):211-225.
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  6.  9
    Raymond De Vries (2005). Framing Neuroethics: A Sociological Assessment of the Neuroethical Imagination. American Journal of Bioethics 5 (2):25-27.
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  7.  9
    L. Kater, R. Houtepen, R. Vries & G. Widdershoven (2003). Health Care Ethics and Health Law in the Dutch Discussion on End-of-Life Decisions: A Historical Analysis of the Dynamics and Development of Both Disciplines. Studies in History and Philosophy of Science Part C 34 (4):669-684.
    Over the past three or four decades, the concept of medical ethics has changed from a limited set of standards to a broad field of debate and research. We define medical ethics as an arena of moral issues in medicine, rather than a specific discipline. This paper examines how the disciplines of health care ethics and health care law have developed and operated within this arena. Our framework highlights the aspects of jurisdiction (Abbott) and the assignment of responsibilities (Gusfield). This (...)
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  8.  3
    S. Y. Kim, L. Schrock, R. M. Wilson, S. A. Frank, R. G. Holloway, K. Kieburtz & R. G. Vries (2008). An Approach to Evaluating the Therapeutic Misconception. IRB: Ethics & Human Research 31 (5):7-14.
    Subjects enrolled in studies testing high risk interventions for incurable or progressive brain diseases may be vulnerable to deficiencies in informed consent, such as the therapeutic misconception. However, the definition and measurement of the therapeutic misconception is a subject of continuing debate. Our qualitative pilot study of persons enrolled in a phase I trial of gene transfer for Parkinson disease suggests potential avenues for both measuring and preventing the therapeutic misconception. Building on earlier literature on the topic, we developed and (...)
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  9. Susan Dorr Goold, Michael A. Neblo, Scott Y. H. Kim, Raymond de Vries, Gene Rowe & Peter Muhlberger (2012). What Is Good Public Deliberation? Hastings Center Report 42 (2):24-26.
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  10. Raymond Vries (2004). How Can We Help? From "Sociology in" to "Sociology of" Bioethics. Journal of Law, Medicine and Ethics 32 (2):279-292.
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  11. Raymond Vries, Nancy Berlinger & Wendy Cadge (2008). Lost in Translation: The Chaplain's Role in Health Care. Hastings Center Report 38 (6):23-27.
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