A human centred innovative approach based on persona in hereditary angioedema
Abstract Background Hereditary Angioedema (HAE) due to C1-inhibitor deficiency (C1INH) is a rare condition, clinically characterised by recurrent swelling. The unpredictability of attacks affects the patients’ quality of life (QoL). HAE patients and their families have vast unmet physical, psycholog...
שמור ב:
| Principais autores: | , , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BMC
2024-08-01
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| סדרה: | Orphanet Journal of Rare Diseases |
| נושאים: | |
| גישה מקוונת: | https://doi.org/10.1186/s13023-024-03302-x |
| תגים: |
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