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Patient Representation and Advocacy for Alzheimer Disease in Germany and Israel
This paper analyses self-declared aims and representation of dementia patient organizations and advocacy groups (POs) in relation to two recent upheavals: the critique of social stigmatization and biomedical research focusing on prediction. Based on twenty-six semi-structured interviews conducted in...
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| Veröffentlicht in: | J Bioeth Inq |
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| Hauptverfasser: | , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Springer Singapore
2018
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6209015/ https://ncbi.nlm.nih.gov/pubmed/30066235 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11673-018-9871-8 |
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