Towards European harmonisation of healthcare for patients with rare immune disorders: outcome from the ERN RITA registries survey.
- DOI
- 10.1186/s13023-020-1308-x
- Published
- 2020 Jan 30
- Container
- Orphanet journal of rare diseases
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1186/s13023-020-1308-x,
title = {Towards European harmonisation of healthcare for patients with rare immune disorders: outcome from the ERN RITA registries survey.},
author = {Papa R and Cant A and Klein C and Little MA and Wulffraat NM and Gattorno M and Ruperto N and ERN RITA Council},
year = {2020},
journal = {Orphanet journal of rare diseases},
doi = {10.1186/s13023-020-1308-x},
url = {https://doi.org/10.1186/s13023-020-1308-x}
}RIS
TY - JOUR TI - Towards European harmonisation of healthcare for patients with rare immune disorders: outcome from the ERN RITA registries survey. AU - Papa R AU - Cant A AU - Klein C AU - Little MA AU - Wulffraat NM AU - Gattorno M AU - Ruperto N AU - ERN RITA Council PY - 2020 JO - Orphanet journal of rare diseases DO - 10.1186/s13023-020-1308-x UR - https://doi.org/10.1186/s13023-020-1308-x ER -
APA
R, P., A, C., C, K., MA, L., NM, W., M, G., N, R., & Council, E. R. (2020). Towards European harmonisation of healthcare for patients with rare immune disorders: outcome from the ERN RITA registries survey.. Orphanet journal of rare diseases. https://doi.org/10.1186/s13023-020-1308-x
Source records
- pubmed · retrieved 2026-09-26T18:22:45.703Z