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  1.  23
    On Pandemics and the Duty to Care: Whose Duty? Who Cares?Carly Ruderman, C. Shawn Tracy, Cécile M. Bensimon, Mark Bernstein, Laura Hawryluck, Randi Z. Shaul & Ross E. G. Upshur - 2006 - BMC Medical Ethics 7 (1):5.
    BackgroundAs a number of commentators have noted, SARS exposed the vulnerabilities of our health care systems and governance structures. Health care professionals and hospital systems that bore the brunt of the SARS outbreak continue to struggle with the aftermath of the crisis. Indeed, HCPs – both in clinical care and in public health – were severely tested by SARS. Unprecedented demands were placed on their skills and expertise, and their personal commitment to their profession was severely tried. Many were exposed (...)
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  2.  30
    A Population‐Based Cohort Study of Ambulatory Care Service Utilization Among Older Adults.Jason X. Nie, Li Wang, C. Shawn Tracy, Rahim Moineddin & Ross E. G. Upshur - 2010 - Journal of Evaluation in Clinical Practice 16 (4):825-831.
  3.  11
    In Whose Interest? Current Issues in Communicating Personal Health Information: A Canadian Perspective.Mark Weitz, Neil Drummond, Dorothy Pringle, Lorraine E. Ferris, Judith Globerman, Philip Hébert, C. Shawn Tracy & Carole Cohen - 2003 - Journal of Law, Medicine and Ethics 31 (2):292-301.
    The continuing spread and development of electronic data interchange in health care settings is fuelling a significant global debate about the practicality, ethics, and legality of such a practice. The uncertainties implicit in this debate are particularly acute in the context of disease or population groups for whom multidisciplinary, multipleagency teamworking has become acknowledged as the “best practice” for providing effective and timely care or support. The greying of the population is a demographic phenomenon that will have a profound impact (...)
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    In Whose Interest? Current Issues in Communicating Personal Health Information: A Canadian Perspective.Mark Weitz, Neil Drummond, Dorothy Pringle, Lorraine E. Ferris, Judith Globerman, Philip Hébert, C. Shawn Tracy & Carole Cohen - 2003 - Journal of Law, Medicine and Ethics 31 (2):292-301.
    The continuing spread and development of electronic data interchange in health care settings is fuelling a significant global debate about the practicality, ethics, and legality of such a practice. The uncertainties implicit in this debate are particularly acute in the context of disease or population groups for whom multidisciplinary, multipleagency teamworking has become acknowledged as the “best practice” for providing effective and timely care or support. The greying of the population is a demographic phenomenon that will have a profound impact (...)
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