WorldCat Identities

Annas, George J.

Overview
Works: 90 works in 247 publications in 1 language and 13,484 library holdings
Genres: Conference proceedings  Trials, litigation, etc  History  Methods 
Roles: Editor
Classifications: KF3823, 344.73041
Publication Timeline
Key
Publications about  George J Annas Publications about George J Annas
Publications by  George J Annas Publications by George J Annas
Most widely held works about George J Annas
 
Most widely held works by George J Annas
The rights of patients : the basic ACLU guide to patient rights by George J Annas ( Book )
13 editions published between 1989 and 2013 in English and held by 1,542 WorldCat member libraries worldwide
George Annas, America's leading proponent of patient rights, spells them out for you in this revised, up-to-date edition of his groundbreaking classic. Thorough, comprehensive, and easy to follow-using a question-and-answer format in much of the text-The Rights of Patients explores all aspects of becoming an informed patient: hospital organization hospital rules emergency treatment admission and discharge the patient rights movement informed consent surgery obstetrical care human experimentation and research privacy and confidentiality care of the dying death, autopsy, and organ donation medical malpractice
American bioethics : crossing human rights and health law boundaries by George J Annas ( Book )
15 editions published between 2004 and 2009 in English and held by 1,120 WorldCat member libraries worldwide
Bioethics was "born in the USA" and the values American bioethics embrace are based on American law, including liberty and justice. This book crosses the borders between bioethics and law, but moves beyond the domestic law/bioethics struggles for dominance by exploring attempts to articulate universal principles based on international human rights. The isolationism of bioethics in the US is not tenable in the wake of scientific triumphs like decoding the human genome, and civilizational tragedies like international terrorism. Annas argues that by crossing boundaries, which have artificially separated bioethics and health law from the international human rights movement, American bioethics can be reborn as a global force for good, instead of serving mainly the purposes of U.S. academics. This thesis is explored in a variety of international contexts such as, terrorism and genetic engineering, and in U.S. domestic disputes such as, patient rights and market medicine. The citizens of the world have created two universal codes: science has sequenced the human genome and the United Nations has produced the Universal Declaration of Human Rights.; The challenge for American bioethics is to combine these two great codes in imaginative and constructive ways to make the world a better, and healthier, place to live
The Nazi doctors and the Nuremberg Code : human rights in human experimentation ( Book )
13 editions published between 1992 and 1995 in English and held by 1,026 WorldCat member libraries worldwide
The atrocities committed by Nazi physicians and researchers during World War II prompted the development of the Nuremberg Code to define the ethics of modern medical experimentation utilizing human subjects. Since its enunciation, the Code has been viewed as one of the cornerstones of modern bioethical thought. The sources and ramifications of this important document are thoroughly discussed in this book by a distinguished roster of contemporary professionals from the fields of history, philosophy, medicine, and law. Contributors also include the chief prosecutor of the Nuremberg Military Tribunal and a survivor of the Mengele twin experiments. The book sheds light on keenly debated issues of both science and jurisprudence, including the ethics of human experimentation; the doctrine of informed consent; and the Code's impact on today's international human rights agenda. The historical setting of the Code's creation, some modern parallels, and the current attitude of German physicians toward the crimes of the Nazi era are discussed in early chapters. The book progresses to a powerful account of the Doctors' Trial at Nuremberg, its resulting verdict, and the Code's development. The Code's contemporary influence on both American and international law is examined in its historical context and discussed in terms of its universality: Are the foundational ethics of the Code as valid today as when it was originally penned? The editors conclude with a chapter on foreseeable future developments and a proposal for an international covenant on human experimentation enforced by an international court. A major work in medical law and ethics, this volume provides stimulating, provocative reading for physicians, legal professionals, bioethicists, historians, biomedical researchers, and concerned laypersons
Genetics and the law by Aubrey Milunsky ( Book )
17 editions published between 1975 and 1995 in English and Undetermined and held by 978 WorldCat member libraries worldwide
Worst case bioethics : death, disaster, and public health by George J Annas ( )
13 editions published between 2010 and 2011 in English and held by 900 WorldCat member libraries worldwide
"Bioethics, still in its infancy, is routinely called on by the government to provide political cover for controversial public health decisions involving the life and death of Americans. Doomsday or worst-case scenarios are often at the heart of these biopolitical decisions. A central feature of science fiction, these scenarios can impart useful insights. But worst-case scenarios, like Frankenstein's monster, can also be unpredictably destructive, undermining both preparedness and the very values, bioethics seeks to promote. Discovering a new flu strain, for example, leads immediately to visions of the 1918 flu pandemic, the worst in human history. Likewise, a "ticking time bomb" scenario leads to the use of physicians for torture, and the all purpose worst case charge of "socialism" threatens to derail meaningful healthcare reform." "In Worst Case Bioethics George Annas employs contemporary disputes involving death and disaster to explore the radical changes underway in public health practice, the application of constitutional law to medicine, and human rights discourse to promote human health and well-being. Worst-case scenarios, especially worst-case bioethics scenarios, distort debate, limit options, rationalize human rights abuses, and undermine equality and social justice. It is, nonetheless, possible to temper worst-case scenarios in ways that promote both the development of a meaningful American bioethics, and a life and liberty affirming global health and human rights movement."--BOOK JACKET
Standard of care : the law of American bioethics by George J Annas ( Book )
9 editions published between 1993 and 1997 in English and Undetermined and held by 891 WorldCat member libraries worldwide
American law, not philosophy or medicine, is the major force shaping American bioethics. This is both because law at its best fosters individual rights, equality, and justice, and because violation of the legal duty or "standard of care" a physician owes a patient can lead to a malpractice suit. The law has therefore had two conflicting impacts on medical ethics: the positive effect of eroding paternalism and replacing it with a patient-centered ethic; and the negative effect of encouraging physicians to be more concerned with avoiding litigation than doing the "right" thing. Standard of Care explores the fundamental value conflicts confronting medicine and society by examining courtroom resolutions of real bioethical disputes, often of constitutional dimension. This case-based approach, which ranges from abortion to euthanasia, from AIDS to organ transplantation, from genetic research to the artificial heart and rationing, illuminates the value choices with which the power (and impotence) of medicine confronts us. George Annas urges health care professionals to go beyond the minimalist legal "standard of care" by promoting a vigorous, patient-centered medical ethics based on respect for human rights and responsibility to both patients and society. If modern medicine is to enhance human life, a reconceptualization of law as the beginning of ethical discourse, rather than as an instrument to end it, is essential. Such a discourse could enrich all our lives by helping us to articulate both a national and international agenda for human rights in health
The rights of patients : the authoritative ACLU guide to the rights of patients by George J Annas ( Book )
5 editions published between 2003 and 2004 in English and held by 816 WorldCat member libraries worldwide
Gene mapping : using law and ethics as guides ( Book )
10 editions published in 1992 in English and held by 789 WorldCat member libraries worldwide
This pathfinding book thoroughly identifies and explores the legal and ethical dimensions of the new genetics and the Human Genome Project. While accepting the goals of modern genetics research, the book takes a critical approach to the Human Genome Project. More precise genetic information will likely result in genetic discrimination, and will threaten genetic privacy in employment and insurance. The way we view disease, normalcy and our own humanness will undergo significant change as clinical medicine becomes increasingly genetics based. We are more than our genes, but mapping them will move society into "genetics territory," and we may act as if our genes determine our destiny. This timely work brings together a group of the nation's leading experts in genetics, medicine, history of science, health, law, philosophy of science, and medical ethics to assess the current state of modern human genetics, and to begin to chart the legal and ethical guidelines needed to prevent the misuse of human genetics from leading to the abuse of human beings. The six sections of the book, read together, map the social policy con tours of modern human genetics. The first part describes the science of the Human Genome Project. The second addresses specific social policy implications, including the relevance of recombinant DNA history, the eugenics legacy, military applications, and issues of race and class in the context of genetic discrimination. Broader philosophical issues, including reductionism and determinism, the concept of disease, and using germline gene therapy to "improve" human beings are discussed in the third part. The fourth is directed at the clinical implications of the new genetics, including privacy and confidentiality, genetic screening, and counseling. The fifth part focuses on the legal and ethical frontiers in genetics, especially procreative liberty, patent issues, and regulatory mechanisms. Finally, a prioritized social policy research agenda is presented which suggests that immediate emphasis be on (1) determining the rules for introducing a new genetic test into medical practice; (2) protecting the confidentiality and privacy of an individual's genetic information; (3) preventing employment and insurance discrimination based on genetics; and (4) exploring how the new genetics will affect our concepts of "disease," "normalcy," and "humanness."
The rights of hospital patients : the basic ACLU guide to a hospital patient's rights by George J Annas ( Book )
10 editions published in 1975 in English and held by 776 WorldCat member libraries worldwide
Judging medicine by George J Annas ( Book )
8 editions published between 1988 and 1990 in English and Undetermined and held by 760 WorldCat member libraries worldwide
The rights of doctors, nurses, and allied health professionals : a health law primer by George J Annas ( Book )
5 editions published in 1981 in English and held by 700 WorldCat member libraries worldwide
Genetics and the law II by National Symposium on Genetics and the Law ( Book )
8 editions published in 1980 in English and Undetermined and held by 523 WorldCat member libraries worldwide
Some choice : law, medicine, and the market by George J Annas ( Book )
4 editions published in 1998 in English and held by 459 WorldCat member libraries worldwide
Informed consent to human experimentation : the subject's dilemma by George J Annas ( Book )
4 editions published in 1977 in English and held by 459 WorldCat member libraries worldwide
Reproductive genetics and the law by Sherman Elias ( Book )
6 editions published in 1987 in English and held by 374 WorldCat member libraries worldwide
Genetics and the law III by National Symposium on Genetics and the Law ( Book )
7 editions published in 1985 in English and held by 364 WorldCat member libraries worldwide
Obstetrics : normal and problem pregnancies by Steven G Gabbe ( Book )
7 editions published between 1996 and 2000 in English and held by 247 WorldCat member libraries worldwide
Electronic version of 1996 textbook
Withholding and withdrawing of life-sustaining treatment for elderly incompetent patients : a review of court decisions and legislative approaches by George J Annas ( Book )
2 editions published in 1985 in English and held by 230 WorldCat member libraries worldwide
Safe alternatives in childbirth : based on the first American NAPSAC conference, May 15, 1976, Arlington, Virginia by American NAPSAC Conference ( Book )
9 editions published between 1976 and 1992 in English and held by 198 WorldCat member libraries worldwide
American health law ( Book )
3 editions published in 1990 in English and held by 158 WorldCat member libraries worldwide
 
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Alternative Names
Annas, George
アナス, ジョージ・J
Languages
English (165)
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