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  1. The Doctor-Proxy Relationship: The Neglected Connection.Nancy Neveloff Dubler - 1995 - Kennedy Institute of Ethics Journal 5 (4):289-306.
    Advance directives have been lauded by scholars and supported by professional organizations, Congress, and the United States Supreme Court. Despite this encouragement, only a small number of capable patients execute living wills or appoint health care agents. When patients do empower proxies, doctors may be uncertain about the scope of their duties and obligations to these persons who, in theory, stand in the shoes of the patient. This article argues for a conscious focus on the ethical duties, emotional supports, and (...)
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  • Family Wishes And Patient Autonomy: Commentary.Stuart J. Youngner & David L. Jackson - 1980 - Hastings Center Report 10 (5):21-22.
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  • Is There a Duty to Die?John Hardwig - 1997 - Hastings Center Report 27 (2):34-42.
    When Richard Lamm made the statement that old people have a duty to die, it was generally shouted down or ridiculed. The whole idea is just too preposterous to entertain. Or too threatening. In fact, a fairly common argument against legalizing physician-assisted suicide is that if it were legal, some people might somehow get the idea that they have a duty to die. These people could only be the victims of twisted moral reasoning or vicious social pressure. It goes without (...)
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  • Case Studies: Family Wishes and Patient Autonomy.Stuart J. Youngner, David L. Jackson & William Ruddick - 1980 - Hastings Center Report 10 (5):21.
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  • The Ends of Human Life: Medical Ethics in a Liberal Polity.Norman Daniels, Troyen A. Brennan & Ezekiel J. Emanuel - 1992 - Hastings Center Report 22 (6):41.
    Book reviewed in this article: Just Doctoring: Medical Ethics in the Liberal State. By Troyen A. Brennan. The Ends of Human Life: Medical Ethics in a Liberal Polity. By Ezekiel J. Emanuel.
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  • Special Supplement: The Ethics of Home Care: Autonomy and Accommodation.Bart Collopy, Nancy Dubler, Connie Zuckerman, Bette-Jane Crigger & Courtney S. Campbell - 1990 - Hastings Center Report 20 (2):1.
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  • The Patient in the Family: An Ethics of Medicine and Families.Hilde Lindemann Nelson & James Lindemann Nelson - 1995 - New York: Routledge. Edited by James Lindemann Nelson.
    The Patient in the Family diagnoses the ways in which the worlds of home and hospital misunderstand each other. The authors explore how medicine, through its new reproductive technologies, is altering the stucture of families, how families can participate more fully in medical decision-making, and how to understand the impact on families of medical advances to extend life but not vitality.
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  • Spousal Understanding of Patient Quality of Life: Implications for Surrogate Decisions.Robert A. Pearlman, Richard F. Uhlmann & Nancy S. Jecker - 1992 - Journal of Clinical Ethics 3 (2):114-121.
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  • Mediating bioethical disputes.Nancy N. Dubler - 1994 - New York: United Hospital Fund of New York. Edited by Leonard J. Marcus.
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  • Medical codes and oaths.Robert M. Veatch - 1995 - Encyclopedia of Bioethics 2.
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  • The Economic Impact of High‐Technology Home Care.Peter S. Arno, Karen A. Bonuck & Robert Padgug - 1994 - Hastings Center Report 24 (5):15-19.
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  • The Family in Medical Decisionmaking.Jeffrey Blustein - 1993 - Hastings Center Report 23 (3):6-13.
    Should the authority to make treatment decisions be extended to the competent patient's family? Neither arguments from fairness nor communitarian concerns justify such an infringement on patient autonomy.
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  • Encyclopedia of bioethics.Robert Veatch & T. W. Reich - forthcoming - Encyclopedia of Bioethics.
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  • Introduction: The Doctor-Proxy Relationship: An Untapped Resource.Linda Farber Post, Jeffrey Blustein & Nancy Neveloff Dubler - 1999 - Journal of Law, Medicine and Ethics 27 (1):5-12.
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  • Being a Burden on Others.Nancy S. Jecker - 1993 - Journal of Clinical Ethics 4 (1):16-20.
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  • Dialogue to Action: Lessons Learned from Some Family Members of Deceased Patients at an Interactive Program in Seven Utah Hospitals.J. Gully, J. VanRiper, C. Grammes, David J. Green, Margaret P. Battin, L. P. Francis & Jay A. Jacobson - 1997 - Journal of Clinical Ethics 8 (4):359-371.
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  • Dialogue to action: lessons learned from some family members of deceased patients at an interactive program in seven Utah hospitals.J. A. Jacobson, L. P. Francis, M. P. Battin, G. J. Green, C. Grammes, J. VanRiper & J. Gully - 1997 - Journal of Clinical Ethics 8 (4):359.
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