Macrophage Activation Syndrome as a Severe Manifestation of Adult's Still's Disease. Hemophagocytic Cells in Ascites-Reference-Cited by-同舟云学术

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Macrophage Activation Syndrome as a Severe Manifestation of Adult's Still's Disease. Hemophagocytic Cells in Ascites

Published:2014-11 Issue:6 Volume:10 Page:420-421
ISSN:2173-5743
Container-title:Reumatología Clínica (English Edition)
language:en
Short-container-title:Reumatología Clínica (English Edition)

Author:

Egües Dubuc César,Uriarte Ecenarro Miren,Errazquin Aguirre Nerea,Belzunegui Otano Joaquín

Publisher

Elsevier BV

Reference10 articles.

1. Reactive hemophagocytic syndrome in adult systemic disease: report of twenty-six cases and literature review;Dhote;Arthritis Rheum,2003

2. Reactive haemophagocytic syndrome in adult-onset Still's disease: a report of six patients and a review of the literature;Arlet;Ann Rheum Dis,2006

3. Syndrome d’activation macrophagique [Macrophage activation syndrome];Karras;Rev Med Intern,2002

4. Diagnostic value of ferritin and glycosylated ferritin in adult onset Still's disease;Fautrel;J Rheumatol,2001

5. Natural killer cell dysfunction is a distinguishing feature of systemic onset juvenile rheumatoid arthritis and macrophage activation syndrome;Villanueva;Arthritis Res Ther,2005

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