David Bourget (Western Ontario)
David Chalmers (ANU, NYU)
Rafael De Clercq
Jack Alan Reynolds
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HEC Forum 22 (2):85-116 (2010)
This article reviews recent developments in health care law, focusing on the engagement of law as a partner in health care innovation. The article addresses: the history and contents of recent United States federal law restricting the use of genetic information by insurers and employers; the recent federal policy recommending routine HIV testing; the recent revision of federal policy regarding the funding of human embryonic stem cell research; the history, current status, and need for future attention to advance directives; the recent emergence of medical–legal partnerships and their benefits for patients; the obesity epidemic and its implications for the child’s right to health under international conventions
|Keywords||The Genetic Information Nondiscrimination Act (GINA) Routine HIV testing Human embryonic stem cell (hESC) research Advance directive Medical-legal partnerships Children’s health rights and obesity|
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References found in this work BETA
Bernard Lo (1994). Resolving Ethical Dilemmas: A Guide for Clinicians. Williams & Wilkins.
Leslie E. Wolf, Bernard Lo & Lawrence O. Gostin (2004). Legal Barriers to Implementing Recommendations for Universal, Routine Prenatal HIV Testing. Journal of Law, Medicine & Ethics 32 (1):137-147.
[author unknown] (2010). National Institutes of Health Guidelines on Human Stem Cell Research. Jahrbuch für Wissenschaft Und Ethik 15:475-484.
Charity Scott (2000). Why Law Pervades Medicine: An Essay On Ethics in Health Care. Notre Dame Journal of Law, Ethics and Public Policy 14 (1):245-304.
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