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Towards European harmonisation of healthcare for patients with rare immune disorders: outcome from the ERN RITA registries survey
The Rare Immunodeficiency, AutoInflammatory and AutoImmune Disease (RITA) network is a European Research Network (ERN) that brings together the leading centres for rare immune disorders. On April 2018 an online survey was sent to all RITA members in order to facilitate the harmonization of data coll...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6993334/ https://www.ncbi.nlm.nih.gov/pubmed/32000824 http://dx.doi.org/10.1186/s13023-020-1308-x |