viernes, 31 de enero de 2020

Towards European harmonisation of healthcare for patients with rare immune disorders: outcome from the ERN RITA registries survey | Orphanet Journal of Rare Diseases | Full Text

Towards European harmonisation of healthcare for patients with rare immune disorders: outcome from the ERN RITA registries survey | Orphanet Journal of Rare Diseases | Full Text

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 onlin...
Authors:Riccardo Papa, Andrew Cant, Christoph Klein, Mark A. Little, Nico M. Wulffraat, Marco Gattorno and Nicolino Ruperto
Citation:Orphanet Journal of Rare Diseases 2020 15:33
Content type:Letter to the Editor
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