Journal of Bioethical Inquiry, 15(3)

Journal cover, purple background with transparent biological material and the journal titleThe Journal of Bioethical Inquiry is a forum for discussing and debating ethical, cultural and social issues arising in medicine, the health sciences and health care in general. Coverage includes core areas of conventional bioethics, such as research, clinical practice and medical technology. The journal also addresses questions of pressing contemporary relevance, such as the implications of current world events for the health of populations, and critical analyses of specific social policies around the world and their likely impact on health and welfare and systems of power. Volume 15 Number 3 is now available online.

Editorial
Embedded Journalists or Empirical Critics? The Nature of The “Gaze” in Bioethics.
Michael A. Ashby & Bronwen Morrell

Recent Developments
Social Media: The Unnamed Plaintiff
Bernadette J. Richards

Critical Response
Forget Evil: Autonomy, the Physician–Patient Relationship, and the Duty to Refer
Jake Greenblum & T. J. Kasperbauer

Critical Perspectives
Parental Moral Distress and Moral Schism in the Neonatal ICU
Gabriella Foe, Jonathan Hellmann & Rebecca A. Greenberg

Critical Perspectives
Ethical Issues of Using CRISPR Technologies for Research on Military Enhancement
Marsha Greene & Zubin Master

Symposium: Collective Representation in Healthcare Policyy
One For All, All For One? Collective Representation in Healthcare Policy
Karin Jongsma, Nitzan Rimon-Zarfaty, Aviad Raz & Silke Schicktanz

Symposium: Collective Representation in Healthcare Policy
Representing Whom? U.K. Health Consumer and Patients’ Organizations in the Policy Process
Rob Baggott & Kathryn L. Jones

Symposium: Collective Representation in Healthcare Policyy
Legislating Patient Representation: A Comparison Between Austrian and German Regulations on Self-Help Organizations as Patient Representatives
Daniela Rojatz, Julia Fischer & Hester Van de Bovenkamp

Symposium: Collective Representation in Healthcare Policy
Representative Claims in Healthcare: Identifying the Variety in Patient Representation
Hester M. van de Bovenkamp & Hans Vollaard

Symposium: Collective Representation in Healthcare Policy
Patient Representation and Advocacy for Alzheimer Disease in Germany and Israel
Silke Schicktanz, Nitzan Rimon-Zarfaty, Aviad Raz & Karin Jongsma

Symposium: Collective Representation in Healthcare Policy
Mitochondrial Replacement Techniques
Jacquelyne Luce

Symposium: Collective Representation in Healthcare Policy
Are ME/CFS Patient Organizations “Militant”?
Charlotte Blease & Keith J. Geraghty

Original Research
Strategies to Guide the Return of Genomic Research Findings: An Australian Perspective
Lisa Eckstein & Margaret Otlowski

Original Research
Medicolegal Complications of Apnoea Testing for Determination of Brain Death
Ariane Lewis & David Greer

Original Research
Commodification and Human Interests
Julian J. Koplin

Original Research
Attitudes Towards the Donation of Human Embryos for Stem Cell Research Among Chinese IVF Patients and Students
Achim Rosemann & Huiyu Luo

Original Research
Responsibility as an Obstacle to Good Policy: The Case of Lifestyle Related Disease
Neil Levy

Original Research
Why Do Medical Professional Regulators Dismiss Most Complaints From Members of the Public? Regulatory Illiteracy, Epistemic Injustice, and Symbolic Power
Orla O’Donovan & Deirdre Madden

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