Journal of Clinical Research & Bioethics

Title Publication Date Language Citations
The Problem of Randomization within a Standard of Care Range: A Case Study2015/01/01
The Use of Placebo and the Right of Autonomy2015/01/01
When is One Trial Enough?2015/01/01
Reluctance to Advance the Age of Measles Immunisation: Ethics of Best Bargain, Policies of Denial, and Programs of Verticality2015/01/01
Polyorchidism Presenting with Testicular Pain and Scrotal Mass2015/01/01
The Emergence of Resourced Research Services2015/01/01
Saving Life or Trumping Autonomy? A Question for Health Care Providers2015/01/01
The Symbolic Relevance of Feedback: Return and Disclosure of Genomic Research Results of Breast Cancer Patients in Belgium, Germany and the UK2015/01/01
Editors & Editorial Board2010/01/01
Reflections on Clinical Ethics2010/01/01
The Philosophy of doing Observational Medicines Safety Research2012/01/01
Are the Voices of Women and Men Equally Represented in Ethics Committees? An Italian Survey2012/01/01
Patient Adherence to Treatment2012/01/01
Assessment of Barriers in Subject Recruitment for Clinical Trials2012/01/01
The Ethics of Care in Biomedical Research Committees2012/01/01
Public Health Ethics: Resource Allocation and the Ethics of Legitimacy2013/01/01
A Drink Best Not Served: Conflicts of Interests When the Alcohol Industry Seeks To Inform Public Health Practice and Policy2013/01/01
The U.S. Regulations and the Protection of Pediatric Subjects2013/01/01
Smallpox and Bioterrorism: History and Evaluation of Current State and Medical Knowledge2011/01/01
Accepting End of Life Care Realities - When the Choices are Limited2013/01/01
Therapeutic Misconception in Early Phase Trials: Relation is the Cure2011/01/01
Asymmetries of Patient Autonomy and Paternalism2011/01/01
Ethical Issues Raised by the Clinical Implementation of New Diagnostic Tools for Genetic Diseases in Children: Array Comparative Genomic Hybridization (aCGH) as a Case Study2015/01/01
Conflict between Paternalism and Autonomy2015/01/01
Genomic Testing and Genomic Care: Are They Talking to Each Other?2015/01/01
Ethical Issues of the Practice of ‘Medicide, Suicide and Laicide’ in the Netherlands after the Euthanasia Law of 20022015/01/01
A Philosophical Analysis of Informed Consent for Whole Genome Sequencing in Biobank Research by use of Beauchamp and Childress’ Four Principles of Biomedical Ethics2015/01/01
Role of Doctor in Euthanasia - Teaching Medical Students - Challenges and Perspectives2015/01/01
Macroscopic and Histopathological Study of the Placenta - An Essential Resource in Litigation Processes2015/01/01
Addressing Benefits, Risks and Consent in Next Generation Sequencing Studies2015/01/01