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This book is about the life of a physician, scientist, psychiatrist, and bioethicist that has been interwoven with the coexistence of the hepatitis C virus (HCV). It entails medical, ethical, spiritual, and historical reflections, as well as the objective and personal history and science of viral hepatitis as well. His life might also be seen as a story of multiple survival episodesnot all related to HCVthat suggests providential oversight.
The Oxford Textbook of Clinical Research Ethics is the first comprehensive and systematic reference on clinical research ethics. Under the editorship of experts from the U.S. National Institutes of Health of the United States, the book's 73 chapters offer a wide-ranging and systematic examination of all aspects of research with human beings. Considering the historical triumphs of research as well as its tragedies, the textbook provides a framework for analyzing the ethical aspects of research studies with human beings. Through both conceptual analysis and systematic reviews of empirical data, the contributors examine issues ranging from scientific validity, fair subject selection, risk benefit ratio, independent review, and informed consent to focused consideration of international research ethics, conflicts of interests, and other aspects of responsible conduct of research. The editors of The Oxford Textbook of Clinical Research Ethics offer a work that critically assesses and advances scholarship in the field of human subjects research. Comprehensive in scope and depth, this book will be a crucial resource for researchers in the medical sciences, as well as teachers and students.
Bound volumes of publications by the faculty of the University of Michigan Department of Pediatrics. Volumes begin during the chairmanship of William Oliver and containing through the chairmanship of Robert P. Kelch.
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Each number is the catalogue of a specific school or college of the University.
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