Search results for 'Terminal care Law and legislation' (try it on Scholar)

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  1. Joan McCarthy (ed.) (2011). End-of-Life Care: Ethics and Law. Cork University Press.score: 546.0
     
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  2. Stefania Negri (ed.) (2012). Self-Determination, Dignity and End-of-Life Care: Regulating Advance Directives in International and Comparative Perspective. M. Nijhoff Pub..score: 450.0
    By providing an interdisciplinary reading of advance directives regulation in international, European and domestic law, this book offers new insights into the most controversial legal issues surrounding the debate over dignity and autonomy ...
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  3. Hamide Tacir (2011). Hastanın Kendi Geleceğini Belirleme Hakkı. Xii Levha.score: 396.0
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  4. Lois L. Shepherd (2009). If That Ever Happens to Me: Making Life and Death Decisions After Terri Schiavo. University of North Carolina Press.score: 276.0
    Disorders of consciousness and the permanent vegetative state -- Legal and political wrangling over Terri's life -- In context--law and ethics -- Terri's wishes -- The limits of evidence -- The implications of surrogacy -- Qualities of life -- Feeding -- The preservation of life -- Respect and care : an alternative framework.
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  5. Sheila McLean (2007). Impairment and Disability: Law and Ethics at the Beginning and End of Life. Routledge-Cavendish.score: 276.0
    pt. 1. Background you need. -- What is brain-compatible teaching -- The old and new of it -- When brain research is applied to the classroom everything will change -- Change can be easy -- We're not in Kansas anymore -- Where's the proof -- Tools for exploring the brain -- Ten reasons to care about brain research -- The evolution of brain models -- Be a brain-smart consumer: recognizing good research -- Action or theory: who wants to read (...)
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  6. Mansoor Elahi (2011). Medical Ethics: A Practical Guide to Patient Care, Related Ethics, Conventions and Laws. Mtro Medical Publishing.score: 225.0
     
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  7. Micheline Garel, Laurence Caeymaex, François Goffinet, Marina Cuttini & Monique Kaminski (2011). Ethically Complex Decisions in the Neonatal Intensive Care Unit: Impact of the New French Legislation on Attitudes and Practices of Physicians and Nurses. Journal of Medical Ethics 37 (4):240-243.score: 208.0
    Next SectionObjectives A statute enacted in 2005 modified the legislative framework of the rights of terminally ill persons in France. Ten years after the EURONIC study, which described the self-reported practices of neonatal caregivers towards ethical decision-making, a new study was conducted to assess the impact of the new law in neonatal intensive care units (NICU) and compare the results reported by EURONIC with current practices. Setting and design The study was carried out in the same two NICU as (...)
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  8. Jeanne Fitzpatrick (2010). A Better Way of Dying: How to Make the Best Choices at the End of Life. Penguin Books.score: 207.0
    Foreword -- Prologue -- Attorney Eileen Fitzpatrick -- Dr. Jeanne Fitzpatrick -- section 1. Death and dying in America -- 1. The need for change : the cautionary tale of Phyllis Shattuck -- Dr. Fitzpatrick tells Phyllis Shattuck's story -- Reflections -- How this book will help -- Lessons to learn -- New name, old concept -- 2. Your right to die -- Your right to die is born : the case of Karen Ann Quinlan -- The Supreme Court weights (...)
     
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  9. Merja Kuuppelomäki (2002). The Decision-Making Process When Starting Terminal Care as Assessed by Nursing Staff. Nursing Ethics 9 (1):20-35.score: 207.0
    This article deals with making decisions about starting terminal care. The results are part of a larger survey on nurses’ conceptions of terminal care in community health centres in Finland. The importance, frequency and timing of decision making as well as communication and the number of investigations and procedures carried out are examined. The relationship between decision making and the size of a health centre’s catchment population is also discussed. The results make it possible to compare (...)
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  10. Sally Sheldon & Michael Thomson (eds.) (1998). Feminist Perspectives on Health Care Law. Cavendish Pub..score: 198.0
    This book brings together new work by some of the foremost writers in the health care law arena. It presents exciting new insights,drawing on feminist theory and methodology to further our understanding of health care law. Whilst the book makes a real contribution to both feminist debates and the analysis of this area of law, it is also accessible to the undergraduate student who is approaching this area of legal scholarship and feminist jurisprudence for the first time. Its (...)
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  11. Judith Hendrick (2004). Law and Ethics. Nelson Thornes.score: 198.0
    Provides an insight into the general principles of the professional-patient relationship.
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  12. Charles Foster (2009). Choosing Life, Choosing Death: The Tyranny of Autonomy in Medical Ethics and Law. Hart Pub..score: 198.0
  13. Michael D. A. Freeman (ed.) (2008). Law and Bioethics / Edited by Michael Freeman. Oxford University Press.score: 198.0
     
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  14. Mark Henaghan (2011). Health Professionals and Trust: The Cure for Healthcare Law and Policy. Routledge-Cavendish.score: 198.0
  15. Robert F. Rizzo (2000). Physician-Assisted Suicide in the United States: The Underlying Factors in Technology, Health Care and Palliative Medicine – Part One. Theoretical Medicine and Bioethics 21 (3):277-289.score: 193.5
    In an age of rapid advances inlife-prolonging treatment, patients and caregivers areincreasingly facing tensions in making end-of-lifedecisions. An examination of the history of healthcare in the United States reveals technological,economic, and medical factors that have contributed tothe problems of terminal care and consequently to themovement of assisted suicide. The movement has itsroots in at least two fundamental perceptions andexpectations. In the age of technological medicineenergized by the profit motive, dying comes at a highprice in suffering and in personal (...)
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  16. Kenneth W. Goodman (ed.) (2010). The Case of Terri Schiavo: Ethics, Politics, and Death in the 21st Century. Oxford University Press.score: 189.0
    The case of Terri Schiavo, a young woman who spent 15 years in a persistent vegetative state, has emerged as a watershed in debates over end-of-life care. While many observers had thought the right to refuse medical treatment was well established, this case split a family, divided a nation, and counfounded physicians, legislators, and many of the people they treated or represented. In renewing debates over the importance of advance directives, the appropriate role of artificial hydration and nutrition, and (...)
     
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  17. Yi-Chen Su (forthcoming). When Ethical Reform Became Law: The Constitutional Concerns Raised by Recent Legislation in Taiwan. Journal of Medical Ethics:2013-101599.score: 185.0
    In an effort at ethical reform, Taiwan recently revised the Hospice Palliative Care Law authorising family members or physicians to make surrogate decisions to discontinue life-sustaining treatment if an incompetent terminally ill patient did not express their wishes while still competent. In particular, Article 7 of the new law authorises the palliative care team, namely the physicians, to act as sole decision-makers on behalf of the incompetent terminally ill patient's best interests if no family member is available. However, (...)
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  18. Alireza Bagheri (2013). Medical Futility: A Cross-National Study. Imperial College Press.score: 180.0
    So-called futile care : the experience of the Unied States -- The reality of medical futility in Brazil -- Medical futility and end-of-lfe issues in Belgium -- The concept of medical futility in Venezuela -- Medical futility in Russian Federation -- Medical futility in Australia -- Medical futility in Japan -- Ethical issues and policy in medical futility in China -- Medical futility in Korea -- Medical futility from Swiss perspective -- Medical futility in Turkey -- Medical futility in (...)
     
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  19. J. Savulescu (2013). Elective Ventilation and Interests. Journal of Medical Ethics 39 (3):129-129.score: 171.0
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  20. Arthur L. Caplan, James J. McCartney & Dominic A. Sisti (eds.) (2006). The Case of Terri Schiavo: Ethics at the End of Life. Prometheus Books.score: 171.0
     
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  21. David Larios Risco & Fernando Abellán-García Sánchez (eds.) (2009). Error Sanitario y Seguridad de Pacientes: Bases Jurídicas Para Un Registro de Sucesos Adversos En El Sistema Nacional de Salud. Comares.score: 171.0
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  22. Anne Rilliet Howald (2004). La Réforme des Régimes de Soins de Santé: Cadre International Et Communautaire, Thématiques Actuelles. Presses Universitaires d'Aix-Marseille.score: 171.0
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  23. Robert F. Weir (1989). Abating Treatment with Critically Ill Patients: Ethical and Legal Limits to the Medical Prolongation of Life. Oxford University Press.score: 171.0
    This book offers an in-depth analysis of the wide range of issues surrounding "passive euthanasia" and "allow-to-die" decisions. The author develops a comprehensive conceptual model that is highly useful for assessing and dealing with real-life situations. He presents an informative historical overview, an evaluation of the clinical settings in which treatment abatement takes place, and an insightful discussion of relevant legal aspects. The result is a clearly articulated ethical analysis that is medically realistic, philosophically sound, and legally viable.
     
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  24. Søren Holm (2008). Best Interests: What Problems in Family Law Should Health Care Law Avoid? [REVIEW] Health Care Analysis 16 (3):252-254.score: 168.0
    This article comments briefly on three specific issues in Shazia Choudhry’s paper “‘Best Interests’ What can healthcare law learn from family law?” The three issues are: (1) the implications of ‘best interests’ and ‘welfare science’ for women within the family law and the health care law context, (2) the risk of capture by the ‘welfare science’ industry, and (3) the proposal that a committee of medical experts and medical ethicists should be set up to provide reports to the Court (...)
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  25. M. Strätling, V. E. Scharf & P. Schmucker (2004). Mental Competence and Surrogate Decision-Making Towards the End of Life. Medicine, Health Care and Philosophy 7 (2):209-215.score: 162.0
    German legislation demands that decisions about the treatment of mentally incompetent patients require an ‘informed consent’. If this was not given by the patient him-/herself before he/she became incompetent, it has to be sought by the physician from a guardian, who has to be formally legitimized before. Additionally this surrogate has to seek the permission of a Court of Guardianship (Vormundschaftsgericht), if he/she intends to consent to interventions, which pose significant risks to the health or the life of the (...)
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  26. André den Exter (ed.) (2010). Human Rights and Biomedicine. Maklu.score: 162.0
     
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  27. Akiva Tatz (2010). Dangerous Disease & Dangerous Therapy in Jewish Medical Ethics: Principles and Practice. Targum Press.score: 162.0
     
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  28. Charles D. Douglas, Ian H. Kerridge & Rachel A. Ankeny (2013). Narratives of 'Terminal Sedation', and the Importance of the Intention-Foresight Distinction in Palliative Care Practice. Bioethics 27 (1):1-11.score: 150.0
    The moral importance of the ‘intention–foresight’ distinction has long been a matter of philosophical controversy, particularly in the context of end-of-life care. Previous empirical research in Australia has suggested that general physicians and surgeons may use analgesic or sedative infusions with ambiguous intentions, their actions sometimes approximating ‘slow euthanasia’. In this paper, we report findings from a qualitative study of 18 Australian palliative care medical specialists, using in-depth interviews to address the use of sedation at the end of (...)
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  29. Virginia Held (2011). Morality, Care, and International Law. Ethics and Global Politics 4 (3).score: 144.0
    Whether we should respect international law is in dispute. In the United States, international law is dismissed by the left as merely promoting the interests of powerful states. It is attacked by the right as irrelevant and an interference with the interests and mission of the United States. And it follows from the arguments of many liberals that in the absence of world government the world is in a Hobbesian state of nature and international law inapplicable. This article reviews the (...)
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  30. George P. Smith (1998). Terminal Sedation as Palliative Care: Revalidating a Right to a Good Death. Cambridge Quarterly of Healthcare Ethics 7 (4):382-387.score: 144.0
    Not everyone finds a in suffering. Indeed, even those who do subscribe to this interpretation recognize the responsibility of each individual to show not only sensitivity and compassion but render assistance to those in distress. Pharmacologic hypnosis, morphine intoxication, and terminal sedation provide their own type of medical to the terminally ill patient suffering unremitting pain. More and more states are enacting legislation that recognizes this need of the dying to receive relief through regulated administration of controlled substances. (...)
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  31. Y. Michael Barilan (2003). Revisiting the Problem of Jewish Bioethics: The Case of Terminal Care. Kennedy Institute of Ethics Journal 13 (2):141-168.score: 139.5
    : This paper examines the main Jewish sources relevant to end-of-life ethics, two Talmudic stories, the early modern code of law (Shulhan Aruch), and contemporary Halakhaic (religious law) responsa. Some Orthodox rabbis object to the use of artificial life support that prolongs the life of a dying patient and permit its active discontinuation when the patient is suffering. Other rabbis believe that every medical measure must be taken in order to prolong life. The context of the discussion is the recent (...)
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  32. Viktoras Justickis & Vidmantas Egidijus Kurapka (2009). Criminogenic Security of Law in the EU and Lithuanian Legislation. Jurisprudence 117 (3):217-238.score: 138.0
    The study focuses on the phenomenon of crime-causing (criminogenic) law. It includes a review of related studies on such laws and their criminal side-effects, the change in the legislator’s liability for effects of enacted laws, and the effects of the legislator’s afflatus on the potential criminogenic effects of law. Of special concern are cases where the legislator is aware of the potential criminogenic side-effects of a new law but carelessly neglects them. The study evaluates the tool for detection of probable (...)
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  33. Leonard M. Fleck (2011). Just Caring: Health Care Rationing, Terminal Illness, and the Medically Least Well Off. Journal of Law, Medicine and Ethics 39 (2):156-171.score: 135.0
    What does it mean to be a “just” and “caring” society in meeting the health care needs of the terminally ill when we have only limited resources to meet virtually unlimited health care needs? That question is the focus of this essay. Put another way: relative to all the other health care needs in our society, especially the need for lifesaving or life-prolonging health care, how high a priority ought the health care needs of persons (...)
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  34. David N. Weisstub (ed.) (1998). Research on Human Subjects: Ethics, Law, and Social Policy. Pergamon.score: 135.0
    There have been serious controversies in the latter part of the 20th century about the roles and functions of scientific and medical research. In whose interests are medical and biomedical experiments conducted and what are the ethical implications of experimentation on subjects unable to give competent consent? From the decades following the Second World War and calls for the global banning of medical research to the cautious return to the notion that in controlled circumstances, medical research on human subjects is (...)
     
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  35. Alan Jotkowitz & Avraham Steinberg (2006). Multiculturalism and End-of-Life Care: The New Israeli Law for the Terminally III Patient. American Journal of Bioethics 6 (5):17 – 19.score: 129.0
  36. Y. Michael Barilan (2007). The New Israeli Law on the Care of the Terminally Ill: Conceptual Innovations Waiting for Implementation. Perspectives in Biology and Medicine 50 (4):557-571.score: 129.0
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  37. Helga Varden (2012). A Kantian Critique of the Care Tradition: Family Law and Systemic Justice. Kantian Review 17 (2):327-356.score: 126.0
    Liberal theories of justice have been rightly criticized for two things by care theorists. First, they have failed to deal with private care relations’ inherent (inter)dependency, asymmetry and particularity. Second, they have been shown unable properly to address the asymmetry and dependency constitutive of care workers’ and care-receivers’ systemic conditions. I apply Kant’s theory of right to show that current care theories unfortunately reproduce similar problems because also they argue on the assumption that good (...) requires only virtuous private individuals. Giving up this assumption enables us to solve the problems regarding both private care relations and systemic injustice. (shrink)
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  38. Hazel Biggs (2001). Euthanasia, Death with Dignity, and the Law. Hart Publishing.score: 120.0
    Machine generated contents note: Table of Cases xi -- Table of legislation xv -- Introduction: Medicine Men, Outlaws and Voluntary Euthanasia 1 -- 1. To Kill or not to Kill; is that the Euthanasia Question? 9 -- Introduction-Why Euthanasia? 9 -- Dead or alive? 16 -- Euthanasia as Homicide 25 -- Euthanasia as Death with Dignity 29 -- 2. Euthanasia and Clinically assisted Death: from Caring to Killing? 35 -- Introduction 35 -- The Indefinite Continuation of Palliative Treatment 38 (...)
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  39. Steven C. Schachter (ed.) (2008). Managing Relationships with Industry: A Physician's Compliance Manual. Elsevier.score: 120.0
    Background -- Overview of legal sources -- Summary of recent prosecutions and investigations -- Applications of law and professional and trade association standards to physician relationships with industry -- Legal and ethical aspects of specific physician's industry financial relationships -- Approaching and adopting effective compliance plans.
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  40. Roberta M. Berry, Lisa Bliss, Sylvia Caley, Paul A. Lombardo & Leslie E. Wolf (2013). Recent Developments in Health Care Law: Culture and Controversy. [REVIEW] HEC Forum 25 (1):1-24.score: 120.0
    This article reviews recent developments in health care law, focusing on controversy at the intersection of health care law and culture. The article addresses: emerging issues in federal regulatory oversight of the rapidly developing market in direct-to-consumer genetic testing, including questions about the role of government oversight and professional mediation of consumer choice; continuing controversies surrounding stem cell research and therapies and the implications of these controversies for healthcare institutions; a controversy in India arising at the intersection of (...)
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  41. Gentian Vyshka & Jera Kruja (2011). Inapplicability of Advance Directives in a Paternalistic Setting: The Case of a Post-Communist Health System. [REVIEW] BMC Medical Ethics 12 (1):12-.score: 118.0
    Background: The Albanian medical system and Albanian health legislation have adopted a paternalistic position with regard to individual decision making. This reflects the practices of a not-so-remote past when state-run facilities and a totalitarian philosophy of medical care were politically imposed. Because of this history, advance directives concerning treatment refusal and do-not-resuscitate decisions are still extremely uncommon in Albania. Medical teams cannot abstain from intervening even when the patient explicitly and repeatedly solicits therapeutic abstinence. The Albanian law on (...)
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  42. John Keown (2002). Euthanasia, Ethics, and Public Policy: An Argument Against Legalisation. Cambridge University Press.score: 117.0
    Whether the law should permit voluntary euthanasia or physician-assisted suicide is one of the most vital questions facing all modern societies. Internationally, the main obstacle to legalisation has proved to be the objection that, even if they were morally acceptable in certain 'hard cases', voluntary euthanasia and physician-assisted suicide could not be effectively controlled; society would slide down a 'slippery slope' to the killing of patients who did not make a free and informed request, or for whom palliative care (...)
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  43. Lance Gable (2011). The Patient Protection and Affordable Care Act, Public Health, and the Elusive Target of Human Rights. Journal of Law, Medicine and Ethics 39 (3):340-354.score: 117.0
    The Patient Protection and Affordable Care Act (ACA) sets in motion a wide range of programs that substantially affected the health system in the United States and signify a moderate but important regulatory shift in the role of the federal government in public health. This article briefly addresses two interesting policy paradoxes about the ACA. First, while the legislation primarily addresses health care financing and insurance and establishes only a few initiatives directly targeting public health, the ACA (...)
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  44. Ine Van Hoyweghen, Klasien Horstman & Rita Schepers (2007). Genetic 'Risk Carriers' and Lifestyle 'Risk Takers'. Which Risks Deserve Our Legal Protection in Insurance? Health Care Analysis 15 (3):179-193.score: 117.0
    Over the past years, one of the most contentious topics in policy debates on genetics has been the use of genetic testing in insurance. In the rush to confront concerns about potential abuses of genetic information, most countries throughout Europe and the US have enacted genetics-specific legislation for insurance. Drawing on current debates on the pros and cons of a genetics-specific legislative approach, this article offers empirical insight into how such legislation works out in insurance practice. To this (...)
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  45. Joseph Boyle (2004). Medical Ethics and Double Effect: The Case of Terminal Sedation. Theoretical Medicine and Bioethics 25 (1):51-60.score: 108.0
    The use of terminal sedation to control theintense discomfort of dying patients appearsboth to be an established practice inpalliative care and to run counter to the moraland legal norm that forbids health careprofessionals from intentionally killingpatients. This raises the worry that therequirements of established palliative care areincompatible with moral and legal opposition toeuthanasia. This paper explains how thedoctrine of double effect can be relied on todistinguish terminal sedation from euthanasia. The doctrine of double effect is rooted (...)
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  46. Iain Brassington (2008). Five Words for Assisted Dying. Law and Philosophy 27 (5):415 - 444.score: 108.0
    Motivated by Lord Joffe’s Assisted Dying for the Terminally Ill Bill, but with one eye on any possible future legislation, I consider the justifications that might be offered for limiting assistance in dying to those who are suffering unbearably from terminal illness. I argue that the terminal illness criterion and the unbearable suffering criterion are not morally defensible separately: that a person need be neither terminally ill (or ill at all), nor suffering unbearably (or suffering at all) (...)
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  47. L. W. Sumner (2011). Assisted Death: A Study in Ethics and Law. Oxford University Press.score: 108.0
    In this timely book L.W. Sumner addresses these issues within the wider context of palliative care for patients in the dying process.
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  48. Karen H. Rothenberg (1996). Feminism, Law, and Bioethics. Kennedy Institute of Ethics Journal 6 (1):69-84.score: 108.0
    : Feminist legal theory provides a healthy skepticism toward legal doctrine and insists that we reexamine even formally gender-neutral rules to uncover problematic assumptions behind them. The article first outlines feminist legal theory from the perspectives of liberal, cultural, and radical feminism. Examples of how each theory influences legal practice, case law, and legislation are highlighted. Each perspective is then applied to a contemporary bioethical issue, egg donation. Following a brief discussion of the common themes shared by feminist jurisprudence, (...)
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  49. M. Berry Roberta, Sylvia Caley Lisa Bliss, A. Lombardo Paul, Jonathan Todres Jerri Nims Rooker & E. Wolf Leslie (forthcoming). Recent Developments in Health Care Law: Partners in Innovation. HEC Forum.score: 108.0
    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 (...)
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  50. Roberta Berry, Lisa Bliss, Sylvia Caley, Paul Lombardo, Jerri Rooker, Jonathan Todres & Leslie Wolf (2010). Recent Developments in Health Care Law: Partners in Innovation. [REVIEW] HEC Forum 22 (2):85-116.score: 108.0
    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 (...)
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