Alerts
Other content recommended for you
- Informed consent for functional MRI research on comatose patients following severe brain injury: balancing the social benefits of research against patient autonomy
- Ethical aspects of research into Alzheimer disease. A European Delphi Study focused on genetic and non-genetic research
- Healthcare professionals’ understanding of the legislation governing research involving adults lacking mental capacity in England and Wales: a national survey
- Protocol for a scoping review to understand what is known about how GPs make decisions with, for and on behalf of patients who lack capacity
- Support needs of carers making proxy healthcare decisions for people with dementia: a systematic review based on the Noblit and Hare meta-ethnographic synthesis of qualitative studies
- Old problems in need of new (narrative) approaches? A young physician–bioethicist’s search for ethical guidance in the practice of physician-assisted dying in the Netherlands
- Ethical issues in Alzheimer’s disease research involving human subjects
- Acknowledging awareness: informing families of individual research results for patients in the vegetative state
- Researching about us without us: exploring research participation and the politics of disability rights in the context of the Mental Capacity Act 2005
- Using informed consent to save trust