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Coding undiagnosed rare disease patients in health information systems: recommendations from the RD-CODE project.
Orphanet J Rare Dis. 2024 Jan 27;19(1):28. doi: 10.1186/s13023-024-03030-2.
Orphanet J Rare Dis. 2024.
PMID: 38280999
Free PMC article.
ORPHAcodes use for the coding of rare diseases: comparison of the accuracy and cross country comparability.
Mazzucato M, Pozza LVD, Facchin P, Angin C, Agius F, Cavero-Carbonell C, Corrochano V, Hanusova K, Kirch K, Lambert D, Lucano C, Maiella S, Panzaru M, Rusu C, Weber S, Zurriaga O, Zvolsky M, Rath A.
Mazzucato M, et al. Among authors: angin c.
Orphanet J Rare Dis. 2023 Sep 4;18(1):267. doi: 10.1186/s13023-023-02864-6.
Orphanet J Rare Dis. 2023.
PMID: 37667299
Free PMC article.
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Overview of patients' cohorts in the French National rare disease registry.
Pichon T, Messiaen C, Soussand L, Angin C, Sandrin A, Elarouci N, Jannot AS; BNDMR infrastructure team.
Pichon T, et al. Among authors: angin c.
Orphanet J Rare Dis. 2023 Jul 3;18(1):176. doi: 10.1186/s13023-023-02725-2.
Orphanet J Rare Dis. 2023.
PMID: 37400917
Free PMC article.
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[Orphanet and its consortium: where to find expert-validated information on rare diseases].
Maiella S, Rath A, Angin C, Mousson F, Kremp O.
Maiella S, et al. Among authors: angin c.
Rev Neurol (Paris). 2013 Feb;169 Suppl 1:S3-8. doi: 10.1016/S0035-3787(13)70052-3.
Rev Neurol (Paris). 2013.
PMID: 23452769
French.
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