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The study of genitourinary tumors is an area of recent rapid growth both in the understanding of disease processes and in the development of new diagnostic and therapeutic modalities. During rapid growth phases within any field, it is desirable to reflect on the current 'state of the art'. It is difficult even for experts in reputed areas of advancement to distinguish true advances from false leads, but it is far more difficult yet for those whose expertise lies in other areas to evaluate important advances. Thus, an objective assessment of evolving areas of investigation in the form of a comprehensive review is of considerable value. we have attempted to provide the reader with an over In t...
This case focuses on a dispute between Dr. William J. Catalona, a renowned prostate cancer researcher and surgeon, and his former employer, Washington University, over the ownership and control of an important collection of human tissue and blood. The case is further complicated by the fact that many of the individual donors--a significant portion of them former or current patients of Dr. Catalona--have been asked to take a position with respect to the disposition of the repository. The case raises important issues of informed consent in human medical research and explores the complicated relationships that exist among various stakeholders in such research. The case also presents insight into conflicts that develop with the commercialization of life science research. The conflicts introduce financial and administrative challenges that test the capacity of policies to anticipate and resolve among research institutions, their employees, and patients.
"Casebook on bioethics and the law for law school students"--
In 1992, at the age of 55, Mr. Lintzenich was diagnosed with prostate cancer. This book is his personal story, told in laymen's terms, spanning over seven years. The step-by-step journey (looking at both the serious and humorous sides of this ordeal) candidly tells about the fears, confusion, and expectations as his life was impacted by prostate cancer. It begins with the shocking diagnosis and examines each step of the process as he learned of the treatment options, and struggled to choose the course of action right for him. The personal and medical information is a compilation of first-hand experience, advice from physicians, literature provided by the hospital, and personal research done ...
This volume provides an alternate history of health law by rewriting key judicial opinions from a feminist perspective. Each chapter includes a rewritten opinion penned by a leading scholar relying exclusively on court precedents and scientific understanding available at the time of the original decision accompanied by commentary from an expert placing the case in historical context and explaining how the feminist judgment might have shaped a different path for subsequent developments. It provides a map of the health law field-where paternalism, individualism, gender stereotypes, and tensions over the public-private divide shape decisions about informed consent, medical and nursing malpractice, the relationships among health care professionals and the institutions where they work, end-of-life care, reproductive health care, biomedical research, ownership of human tissues and cells, the influence of religious directives on health care standards, health care discrimination, long-term care, private health insurance, Medicaid coverage, the Affordable Care Act, and more.
Each issue lists papers published during the preceding year.
Each issue lists papers published during the preceding year.
This book provides in-depth analyses of a wide range of topics surrounding ethical issues in community and patient stakeholder–engaged health research, and highlights where consensus exists, is emerging, or remains elusive. Topics in this book cover the history of stakeholder engagement in health research; how codes of ethics and regulations have (or have not) addressed stakeholder engagement; how to promote equitable collaboration; the ethical perspectives of different stakeholders; and the unique challenges posed by stakeholder- engaged research to the protection of human research participants and the research ethics review process. The book includes discussion of unique issues that arise in stakeholder engagement relevant to different populations, settings, and research designs. This book is relevant for anyone with a role or interest in stakeholder-engaged research, including patient and community research partners; academic researchers; research ethics scholars and educators; and funders.