ロード中...

Familial haemophagocytic lymphohistiocytosis: two case reports

Haemophagocytic lymphohistiocytosis (HLH) is a life threatening inflammatory syndrome, which presents a highly stimulated but ineffective immune response with severe hypercytokinaemia. HLH, primary or secondary, is characterised by prolonged fever and hepatosplenomegaly associated with pancytopenia,...

詳細記述

保存先:
書誌詳細
主要な著者: Ferreira, Marta, Martins, Joana, Silvestre, Catarina, Abadesso, Clara, Matias, Ester, Loureiro, Helena, Figueiredo, António, Dias, Alexandra, Almeida, Helena
フォーマット: Artigo
言語:Inglês
出版事項: BMJ Publishing Group 2010
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3047491/
https://ncbi.nlm.nih.gov/pubmed/22736603
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr.11.2009.2463
タグ: タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!