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...

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Detalles Bibliográficos
Autores principales: Papa, Riccardo, Cant, Andrew, Klein, Christoph, Little, Mark A., Wulffraat, Nico M., Gattorno, Marco, Ruperto, Nicolino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Letter to the Editor
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

Internet

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

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