Health Sciences, Medical Ethics.
Overview
| Works: | 28 works in 0 publications in 0 languages | |
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Titles
The metaphysics of dementia: The intersection of personal identity and clinical ethics.
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Compulsory death: A historiographic study of the eugenics and euthanasia movements in Nazi Germany.
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IRB stakeholders: Protecting human research participants through a culture of conscience in a community based participatory research model: An exploratory study.
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Transformations in Health Policy: An Analysis of Alzheimer's Disease Testing, Medicaid Enrollment, and Insurance Market Concentration.
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Suicidal crisis and life-threatening illness: A narrative inquiry.
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Something to Think About: Informing Canadians about Ethical Concerns in Medical Tourism.
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A distinction without a moral difference? An essay on the difference between palliative sedation and physician-assisted death.
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Clinical trials, informed consent, & emergency medicine: A systematic literature review.
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The impact of Senate Bill 1301 on patient safety culture and the financial stability of Central California acute care hospitals.
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The contribution of African traditional medicine for a model of relational autonomy in informed consent.
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Expert on her own Body: Contested Framings of Risk and Expertise in Discourses on Unassisted Childbirth.
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A good death: The politics of physician assisted suicide in Hawai'i.
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Purple in the Morning, Blue in the Afternoon, Orange in the Evening: A Genealogical Analysis of Depressive Disorders in the American Psychiatric Association's Diagnostic and Statistical Manual, Fifth Edition.
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Contradictions in stem cell research education amongst science educators and Buddhist, Christian and Muslim theologians.
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An ethics survey of religious beliefs and reproductive counseling practices of Roman Catholic, Lutheran, and Jewish clergy.
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Ethics education in neonatology: The past, the present, and hope for a future.
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Community engagement in research: Lessons from the clinical and translational science award program and the development of a framework to determine the ethical duty to engage communties in research.
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"We get patients": Understanding the culture of patient recruitment organizations.
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Developpement d'une approche de regulation des essais cliniques dans un contexte de pays en developpement: Le cas du Mali.
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Revising the philosophical foundation for informed consent guidelines in international research on human subjects.
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Improving the quality of informed consent for clincal research participation.
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