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dc.contributor.authorBousfiha, Aziz-
dc.contributor.authorJeddane, Leïla-
dc.contributor.authorPicard, Capucine-
dc.contributor.authorAilal, Fatima-
dc.contributor.authorGaspar, H. Bobby-
dc.contributor.authorFranco Restrepo, José Luis-
dc.date.accessioned2021-10-10T15:15:09Z-
dc.date.available2021-10-10T15:15:09Z-
dc.date.issued2017-
dc.identifier.citationBousfiha A, Jeddane L, Picard C, Ailal F, Bobby Gaspar H, Al-Herz W, Chatila T, Crow YJ, Cunningham-Rundles C, Etzioni A, Franco JL, Holland SM, Klein C, Morio T, Ochs HD, Oksenhendler E, Puck J, Tang MLK, Tangye SG, Torgerson TR, Casanova JL, Sullivan KE. The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies. J Clin Immunol. 2018 Jan;38(1):129-143. doi: 10.1007/s10875-017-0465-8.spa
dc.identifier.issn0271-9142-
dc.identifier.urihttp://hdl.handle.net/10495/23080-
dc.description.abstractABSTRACT: Since the 1990s, the International Union of Immunological Societies (IUIS) PID expert committee (EC), now called Inborn Errors of Immunity Committee, has published every other year a classification of the inborn errors of immunity. This complete catalog serves as a reference for immunologists and researchers worldwide. However, it was unadapted for clinicians at the bedside. For those, the IUIS PID EC is now publishing a phenotypical classification since 2013, which proved to be more user-friendly. There are now 320 single-gene inborn errors of immunity underlying phenotypes as diverse as infection, malignancy, allergy, auto-immunity, and auto-inflammation. We herein propose the revised 2017 phenotypic classification, based on the accompanying 2017 IUIS Inborn Errors of Immunity Committee classification.spa
dc.format.extent15spa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherSpringerspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by-nc/2.5/co/*
dc.titleThe 2017 IUIS Phenotypic Classification for Primary Immunodeficienciesspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupInmunodeficiencias Primariasspa
dc.identifier.doi10.1007/s10875-017-0465-8-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn1573-2592-
oaire.citationtitleJournal of Clinical Immunologyspa
oaire.citationstartpage129spa
oaire.citationendpage143spa
oaire.citationvolume38spa
oaire.citationissue1spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by/4.0/spa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsSíndromes de Inmunodeficiencia-
dc.subject.decsImmunologic Deficiency Syndromes-
dc.subject.decsClasificación-
dc.subject.decsClassification-
dc.subject.proposalPhenotypicspa
dc.subject.proposalInborn errors of immunityspa
dc.subject.proposalUnión Internacional de las Sociedades Inmunológicas (IUIS)spa
dc.subject.proposalFenotípicaspa
dc.description.researchgroupidCOL0012426spa
dc.relation.ispartofjournalabbrevJ. Clin. Immunol.spa
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