Diagnosing XLP1 in patients with hemophagocytic lymphohistiocytosis

BACKGROUND: Hemophagocytic Lymphohistiocytosis (HLH) is a life-threatening, heterogeneous, hyper-inflammmatory disorder. Prompt identification of inherited forms resulting from mutation in genes involved in cellular cytotoxicity can be crucial. X-linked lymphoproliferative disease 1 (XLP1), due to m...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:J Allergy Clin Immunol
Main Authors: Meazza, Raffaella, Tuberosa, Claudia, Cetica, Valentina, Falco, Michela, Parolini, Silvia, Grieve, Sam, Griffiths, Gillian M., Sieni, Elena, Marcenaro, Stefania, Micalizzi, Concetta, Montin, Davide, Fagioli, Franca, Moretta, Alessandro, Mingari, Maria C., Moretta, Lorenzo, Notarangelo, Luigi D., Bottino, Cristina, Aricò, Maurizio, Pende, Daniela
Formato: Artigo
Idioma:Inglês
Publicado em: 2014
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7611500/
https://ncbi.nlm.nih.gov/pubmed/24985396
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jaci.2014.04.043
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados