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...

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Detaylı Bibliyografya
Yayımlandı:J Allergy Clin Immunol
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2014
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Article
Online Erişim: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
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