Towards European harmonisation of healthcare for patients with rare immune disorders: outcome from the ERN RITA registries survey

Towards European harmonisation of healthcare for patients with rare immune disorders: outcome from the ERN RITA registries survey

Abstract 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...

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Bibliographic Details
Main Authors: Riccardo Papa, Andrew Cant, Christoph Klein, Mark A. Little, Nico M. Wulffraat, Marco Gattorno, Nicolino Ruperto, on behalf of ERN RITA Council
Format: Article
Language:English
Published: BMC 2020-01-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Primary immunodeficiency
Autoinflammatory diseases
Autoimmune disorders
European research network
Disease registry
Online Access:https://doi.org/10.1186/s13023-020-1308-x

Internet

https://doi.org/10.1186/s13023-020-1308-x

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