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"Human Experimentation history Europe."
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Blood work : a tale of medicine and murder in the scientific revolution
A sharp-eyed expose of the deadly politics, murderous plots, and cutthroat rivalries behind the first blood transfusions in seventeenth-century Europe.
Victims and Survivors of Nazi Human Experiments
2015,2014
While the coerced human experiments are notorious among all the atrocities under National Socialism, they have been marginalised by mainstream historians. This book seeks to remedy the marginalisation, and to place the experiments in the context of the broad history of National Socialism and the Holocaust. Paul Weindling bases this study on the reconstruction of a victim group through individual victims’ life histories, and by weaving the victims’ experiences collectively together in terms of different groupings, especially gender, ethnicity and religion, age, and nationality. The timing of the experiments, where they occurred, how many victims there were, and who they were, is analysed, as are hitherto under-researched aspects such as Nazi anatomy and executions. The experiments are also linked, more broadly, to major elements in the dynamic and fluid Nazi power structure and the implementation of racial policies. The approach is informed by social history from below, exploring both the rationales and motives of perpetrators, but assessing these critically in the light of victim narratives.
Elements for Adequate Informed Consent in the Surgical Context
2014
Given a history of atrocities and violations of ethical principles, several documents and regulations have been issued by a wide variety of organizations. They aim at ensuring that health care and clinical research adhere to defined ethical principles. A fundamental component was devised to ensure that the individual has been provided the necessary information to make an informed decision regarding health care or participation in clinical research. This article summarizes the history and regulations for informed consent and discusses suggested components for adequate consent forms for daily clinical practice in surgery as well as clinical research.
Journal Article
War Crimes in Japan-Occupied Indonesia
2015
Shortly after Pearl Harbor, the Japanese Imperial Army invaded the Dutch East Indies, now known as Indonesia. A deceitful campaign promoting Asian brotherhood recruited and coerced young Indonesian men to support the Japanese occupation with the sinister outcome that several million of them were worked to death or summarily killed as expendable slave laborers, orromusha, as they were called.
While many romusha disappeared from the record, nine hundred were known victims of a brutal and immoral medical experiment perpetuated by an increasingly desperate Imperial Japan. In anticipation of a land assault, the Japanese needed a means to protect their troops from tetanus, and they used these nine hundred men as human guinea pigs to test an insufficiently vetted vaccine. Within days, all nine hundred suffered the protracted, agonizing death of acute tetanus.
With the Allied forces poised for victory, the Japanese needed a scapegoat for this well-documented incident if they were to avoid war-crimes prosecution. They brutally tortured Achmad Mochtar, a native Indonesian and renowned scientist, along with his colleagues at the Eijkman Institute in Batavia (now Jakarta), until Mochtar signed a confession to the murders in exchange for the liberty of his fellow scientists. The Japanese beheaded Mochtar weeks before the war ended.War Crimes in Japan-Occupied Indonesiaunravels the deceit of the Japanese Army, the reasons for the mass murder of the romusha, and Mochtar's heroic role in these tragic events. The end result finds justice for Mochtar and reveals the true extent of one of the least recognized war crimes of World War II.
Embryo Politics
2011,2017
Since the first fertilization of a human egg in the laboratory in 1968, scientific and technological breakthroughs have raised ethical dilemmas and generated policy controversies on both sides of the Atlantic. Embryo, stem cell, and cloning research have provoked impassioned political debate about their religious, moral, legal, and practical implications. National governments make rules that govern the creation, destruction, and use of embryos in the laboratory-but they do so in profoundly different ways.
InEmbryo Politics, Thomas Banchoff provides a comprehensive overview of political struggles aboutembryo research during four decades in four countries-the United States, the United Kingdom, Germany, and France. Banchoff's book, the first of its kind, demonstrates the impact of particular national histories and institutions on very different patterns of national governance. Over time, he argues, partisan debate and religious-secular polarization have come to overshadow ethical reflection and political deliberation on the moral status of the embryo and the promise of biomedical research. Only by recovering a robust and public ethical debate will we be able to govern revolutionary life-science technologies effectively and responsibly into the future.
Science must acknowledge its past mistakes and crimes
2017
Injustice in the name of research should not be forgotten — nor should those injured by scientists.
Journal Article
Veganic farming in the United States: farmer perceptions, motivations, and experiences
2021
Veganic agriculture, often described as farming that is free of synthetic and animal-based inputs, represents an alternative to chemical-based industrial agriculture and the prevailing alternative, organic agriculture, respectively. Despite the promise of veganic methods in diverse realms such as food safety, environmental sustainability, and animal liberation, it has a small literature base. This article draws primarily on interviews conducted in 2018 with 25 veganic farmers from 19 farms in the United States to establish some baseline empirical research on this farming community. Its qualitative perspectives illuminate farmer perceptions of and experiences with veganic growing, including definitions, knowledge acquisition, values, and challenges. Results highlight a lack of agreement about the meaning of veganic agriculture in terms of allowable inputs and scope. Participants have drawn on a wide array of veganic and non-veganic resources to ascend their veganic production learning curves, also relying on experimentation and trial-and-error. Their farming is motivated by a diversity of real and perceived benefits, most notably consistency with veganism, food safety advantages, and plant and soil health benefits. Veganic product sourcing and the dearth of veganic agriculture-specific resources present considerable challenges to farmers. The article briefly discusses possibilities for developing veganic agriculture in the United States, such as through a US-based certification system and farmers’ associations, based on considerations of the trajectory of the US organic farming movement and veganic developments in Europe. Finally, the article suggests the importance of expanded research into soil health and fertility in plant-based systems to support practicing and potential veganic farmers.
Journal Article
Epistemological Dizziness in the Psychology Laboratory: Lively Subjects, Anxious Experimenters, and Experimental Relations, 1950–1970
2015
Since the demise of introspective techniques in the early twentieth century, experimental psychology has largely assumed an administrative arrangement between experimenters and subjects wherein subjects respond to experimenters’ instructions and experimenters meticulously constrain that relationship through experimental controls. During the postwar era this standard arrangement came to be questioned, initiating reflections that resonated with Cold War anxieties about the nature of the subjects and the experimenters alike. Albeit relatively short lived, these interrogations of laboratory relationships gave rise to unconventional testimonies and critiques of experimental method and epistemology. Researchers voiced serious concerns about the honesty and normality of subjects, the politics of the laboratory, and their own experimental conduct. Their reflective commentaries record the intimacy of subject and experimenter relations and the plentiful cultural materials that constituted the experimental situation, revealing the permeable boundaries between laboratory and everyday life.
Journal Article
Cancer clinical trials in the era of genomic signatures: Biomedical innovation, clinical utility, and regulatory-scientific hybrids
by
Bourret, Pascale
,
Keating, Peter
,
Cambrosio, Alberto
in
Biomedicine
,
Breast Cancer
,
Breast Neoplasms - genetics
2011
The paper examines two large-scale, North American and European clinical trials designed to validate two commercially available genomic tumor signatures that predict a patient's risk of breast cancer recurrence and response to chemotherapy. The paper builds on empirical evidence from the two trials to explore the emergence of diverse regulatory-scientific hybrids; that is, the paper discusses configurations of genomic practice and bioclinical work that depend on linkages between technical, commercial, patient, clinical, and legal interests and institutions. The development of the genomic signatures for each trial - Oncotype DX and MammaPrint - has followed quite different routes. Oncotype began as a commercial platform: the company that produced it did not discover a signature but rather constructed it by asking users at every step what clinical question they wanted the signature to answer and what data would be credible in that regard. The test has been designed to minimally disrupt existing clinical workflows. MammaPrint, on the other hand, began as a breast cancer signature: the researchers who discovered it, at the Netherlands Cancer Institute (NKI), established a company to commercialize it as a test after the fact. MammaPrint requires a change in pathologists' routines. Thus, while these two trials signify a new departure for clinical cancer trials on a number of levels - they both incorporate new models of interaction between biotech companies and public research, and they both aim to establish the clinical relevance of genomic markers - they also embody different socio-technical scripts: one attempts to accommodate established routines, while the other openly challenges prevailing evidential hierarchies and existing biomédical configurations.
Journal Article