Works by Jessica Berg ( view other items matching `Jessica Berg`, view all matches )
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Jessica Berg [8]Jessica W. Berg [6]Jessica Wilen Berg [2]

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  1. Jessica Berg (2012). Response to Open Peer Commentaries on “Surrogate Decision Making in the Internet Age”. American Journal of Bioethics 12 (10):W1-W2.
    The American Journal of Bioethics, Volume 12, Issue 10, Page W1-W2, October 2012.
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  2. Jessica Berg (2012). Surrogate Decision Making in the Internet Age. American Journal of Bioethics 12 (10):28-33.
    The computer revolution has had an enormous effect on all aspects of the practice of medicine, yet little thought has been given to the role of social media in identifying treatment choices for incompetent patients. We are currently living in the ?Internet age? and many people have integrated social media into all aspects of their lives. As use becomes more prevalent, and as users age, social media are more likely to be viewed as a source of information regarding medical care (...)
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  3. Jessica Berg & Nicole Deming (2011). New Rules for Research with Human Participants? Hastings Center Report 41 (6):10-11.
    In July, the Department of Health and Human Services and the Office of Science and Technology Policy published an advance notice of proposed rulemaking (ANPRM) proposing sweeping changes to the rules governing oversight of research on human subjects—changes aimed at “better protect[ing] human subjects who are involved in research, while facilitating valuable research and reducing burden, delay, and ambiguity for investigators.”1 The process is likely to amend not only the core regulation on human-subjects research (known as the “common rule”), but (...)
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  4. Jessica Berg (2010). Review of The Ethics of Consent , Eds. Franklin G. Miller and Alan Wertheimer. [REVIEW] American Journal of Bioethics 10 (7):71-72.
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  5. Jessica Wilen Berg (2010). What Is Left of Charity Care After Health Reform? Hastings Center Report 40 (4):12-13.
    The passage of the Patient Protection and Affordable Care Act on March 23, 2010, significantly changes the health care landscape. But even with the considerable expansion of insurance, many people will still lack coverage. When fully implemented, the act is designed only to cover about thirty-two million of the forty-six million uninsured Americans. Illegal aliens are specifically excluded. For others, implementation is not immediate; the so-called individual mandate, for example, does not take effect until 2014, and there are exceptions for (...)
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  6. Maxwell J. Mehlman & Jessica W. Berg (2008). Human Subjects Protections in Biomedical Enhancement Research: Assessing Risk and Benefit and Obtaining Informed Consent. Journal of Law, Medicine and Ethics 36 (3):546-549.
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  7. Jessica Berg (2007). Review of Side Effects, DVD All Regions, 90 Minutes, Hummingbird Pictures, USA, 2006; and Money Talks: Profits Before Patient Safety, DVD Region 1, 50 Minutes, Hummingbird Pictures, USA, 2006. [REVIEW] American Journal of Bioethics 7 (3):58-58.
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  8. Jessica Berg (2006). A Qualified Defense of Legal Disclosure Requirements. American Journal of Bioethics 6 (2):25 – 26.
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  9. Jessica W. Berg (2006). Smokescreen. Hastings Center Report 36 (4):C3-C3.
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  10. Jessica Berg & Nicholas King (2006). Strange Bedfellows? Reflections on Bioethics' Role in Disaster Response Planning. American Journal of Bioethics 6 (5):3 – 5.
    This essay considers the potential role of bioethics in disaster response planning and preparedness. Bioethicists can make substantial contributions, by ensuring that decision-making and distribution of resources during crises is carried out in a fair and just manner, as well as by examining the assumptions upon which disaster planning are based. Bioethicists should also be aware of potential pitfalls of overly-hasty engagement with this new field.
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  11. Patricia A. Marshall & Jessica W. Berg (2006). Protecting Communities in Biomedical Research. American Journal of Bioethics 6 (3):28 – 30.
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  12. Jessica Berg (2004). You Say Person, I Say Property: Does It Really Matter What We Call an Embryo? American Journal of Bioethics 4 (1):17 – 18.
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  13. Jessica W. Berg (2001). Risky Business: Evaluating Oocyte Donation. American Journal of Bioethics 1 (4):18 – 19.
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  14. David J. Doukas & Jessica W. Berg (2001). The Family Covenant and Genetic Testing. American Journal of Bioethics 1 (3):2 – 10.
    The physician-patient relationship has changed over the last several decades, requiring a systematic reevaluation of the competing demands of patients, physicians, and families. In the era of genetic testing, using a model of patient care known as the family covenant may prove effective in accounting for these demands. The family covenant articulates the roles of the physician, patient, and the family prior to genetic testing, as the participants consensually define them. The initial agreement defines the boundaries of autonomy and benefit (...)
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  15. Jessica Wilen Berg (1996). Legal and Ethical Complexities of Consent with Cognitively Impaired Research Subjects: Proposed Guidelines. Journal of Law, Medicine and Ethics 24 (1):18-35.
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