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Título : The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies
Autor : Bousfiha, Aziz
Jeddane, Leïla
Picard, Capucine
Ailal, Fatima
Gaspar, H. Bobby
Franco Restrepo, José Luis
metadata.dc.subject.*: Síndromes de Inmunodeficiencia
Immunologic Deficiency Syndromes
Clasificación
Classification
Phenotypic
Inborn errors of immunity
Unión Internacional de las Sociedades Inmunológicas (IUIS)
Fenotípica
Fecha de publicación : 2017
Editorial : Springer
Citación : Bousfiha 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.
Resumen : ABSTRACT: 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.
metadata.dc.identifier.eissn: 1573-2592
ISSN : 0271-9142
metadata.dc.identifier.doi: 10.1007/s10875-017-0465-8
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