Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12530/29383
Title: Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study.
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Issue Date: Mar-2018
Citation: J. Allergy Clin. Immunol..2018 Mar;(141)3:1036-1049.e5
Abstract: Immunodysregulation polyendocrinopathy enteropathy x-linked (IPEX) syndrome is a monogenic autoimmune disease caused by FOXP3 mutations. Because it is a rare disease, the natural history and response to treatments, including allogeneic hematopoietic stem cell transplantation (HSCT) and immunosuppression (IS), have not been thoroughly examined.
PMID: 29241729
URI: https://hdl.handle.net/20.500.12530/29383
Rights: openAccess
Appears in Collections:Fundaciones e Institutos de Investigación > FIB H. Infantil U. Niño Jesús > Artículos

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