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Jessica W. Berg [6]Jessica Wilen Berg [3]
  1. Maxwell J. Mehlman, Jessica W. Berg, Eric T. Juengst & Eric Kodish (2011). Ethical and Legal Issues in Enhancement Research on Human Subjects. Cambridge Quarterly of Healthcare Ethics 20 (1):30--45.
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  2. Jay Baruch, Jessica Wilen Berg, Jeffrey T. Berger, Nancy Berlinger, James L. Bernat, J. Andrew Billings, Larry R. Churchill, Richard Payne, Herbert J. Bonifacio & Annie Janvier (2010). Following is the Comprehensive Index for Volume 40 of the Hastings Center Report, Covering All Feature Material From 2010. Letters Have Not Been Included. Ffl Complete Issues Are Available for Volume 40 (2010) and May Be Purchased From the Cir-Culation Department, The Hastings Center, 21 Malcolm Gordon Road, Garrison, NY 10524; Tel.:(845) 424-4040; Fax:(845) 424-4545; E-Mail: Publications@ Thehastingscenter. Org. [REVIEW] Hastings Center Report 40.
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  3. 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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  4. 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.
  5. Jessica W. Berg (2006). Smokescreen. Hastings Center Report 36 (4):C3-C3.
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  6. Patricia A. Marshall & Jessica W. Berg (2006). Protecting Communities in Biomedical Research. American Journal of Bioethics 6 (3):28 – 30.
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  7. Jessica W. Berg (2001). Risky Business: Evaluating Oocyte Donation. American Journal of Bioethics 1 (4):18 – 19.
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  8. 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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  9. 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.