Making sense of the cytokine storm: a conceptual framework for understanding, diagnosing, and treating hemophagocytic syndromes
about
Review: is there a window of opportunity for treatment of systemic juvenile idiopathic arthritis?[Hemophagocytic lymphohistiocytosis : A diagnostic challenge on the ICU].Hemophagocytic lymphohistiocytosis complicating erythroleukemia in a child with monosomy 7: a case report and review of the literature.Hemophagocytic lymphohistiocytosis secondary to infections: a tropical experience!Janus kinase inhibition lessens inflammation and ameliorates disease in murine models of hemophagocytic lymphohistiocytosisIDO1 Deficiency Does Not Affect Disease in Mouse Models of Systemic Juvenile Idiopathic Arthritis and Secondary Hemophagocytic Lymphohistiocytosis.Clinical utility of soluble interleukin-2 receptor in hemophagocytic syndromes: a systematic scoping review.Hemophagocytic lymphohistiocytosis as a paraneoplastic syndrome associated with ovarian dysgerminomaIntravascular large B-cell lymphoma associated with silicone breast implant, HLA-DRB1*11:01, and HLA-DQB1*03:01 manifesting as macrophage activation syndrome and with severe neurological symptoms: a case report.Hyperinflammation, rather than hemophagocytosis, is the common link between macrophage activation syndrome and hemophagocytic lymphohistiocytosis.Complications of systemic juvenile idiopathic arthritis: risk factors and management recommendations.Canakinumab for the treatment of active systemic juvenile idiopathic arthritis.Diagnosing haemophagocytic syndrome.The clinical utility of splenic fluorodeoxyglucose uptake for diagnosis and prognosis in patients with macrophage activation syndrome.Clinical characteristics, prognostic factors, and outcomes of adult patients with hemophagocytic lymphohistiocytosis.Rare cause of natural death in forensic setting: hemophagocytic syndrome.Hemophagocytic lymphohistiocytosis: a rare diagnosis, an even rarer opportunity to appraise our understanding of the immune system.EBV-HLH children with reductions in CD4+ T cells and excessive activation of CD8+ T cells.Hemophagocytic lymphohistiocytosis secondary to Falciparum malaria in a 5 year-old boy.IL-10 distinguishes a unique population of activated, effector-like CD8+ T cells in murine acute liver inflammation.Fatal Outcome of Imatinib in a Patient with Idiopathic Hypereosinophilic Syndrome.
P2860
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P2860
Making sense of the cytokine storm: a conceptual framework for understanding, diagnosing, and treating hemophagocytic syndromes
description
2012 nî lūn-bûn
@nan
2012 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Making sense of the cytokine s ...... ating hemophagocytic syndromes
@ast
Making sense of the cytokine s ...... ating hemophagocytic syndromes
@en
Making sense of the cytokine s ...... ating hemophagocytic syndromes
@nl
type
label
Making sense of the cytokine s ...... ating hemophagocytic syndromes
@ast
Making sense of the cytokine s ...... ating hemophagocytic syndromes
@en
Making sense of the cytokine s ...... ating hemophagocytic syndromes
@nl
prefLabel
Making sense of the cytokine s ...... ating hemophagocytic syndromes
@ast
Making sense of the cytokine s ...... ating hemophagocytic syndromes
@en
Making sense of the cytokine s ...... ating hemophagocytic syndromes
@nl
P2860
P3181
P1476
Making sense of the cytokine s ...... ating hemophagocytic syndromes
@en
P2093
Edward M Behrens
P2860
P304
P3181
P356
10.1016/J.PCL.2012.03.002
P407
P577
2012-04-01T00:00:00Z