Hemophagocytic lymphohistiocytosis associated with anaplasmosis

Hemophagocytic lymphohistiocytosis (HLH) is a hyperinflammatory syndrome characterized by unregulated macrophage and T-lymphocyte activation resulting in cytokine overproduction and subsequent histiocytic phagocytosis. Variant infections, particularly viruses have been postulated as the inciting fac...

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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Tamara M Johnson, Melinda S Brown, Mohamed Rabbat, Jihad Slim
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Wolters Kluwer Medknow Publications 2017-01-01
Saila:Journal of Global Infectious Diseases
Gaiak:
Anaplasmosis
hemophagocytic lymphohistiocytosis
hemophagocytic syndrome
Sarrera elektronikoa:http://www.jgid.org/article.asp?issn=0974-777X;year=2017;volume=9;issue=2;spage=76;epage=78;aulast=Johnson
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