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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...

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Detalhes bibliográficos
Publicado no:Orphanet J Rare Dis
Main Authors: Papa, Riccardo, Cant, Andrew, Klein, Christoph, Little, Mark A., Wulffraat, Nico M., Gattorno, Marco, Ruperto, Nicolino
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2020
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6993334/
https://ncbi.nlm.nih.gov/pubmed/32000824
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-020-1308-x
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