Inherited defects causing hemophagocytic lymphohistiocytic syndrome
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[Hemophagocytic lymphohistiocytosis : A diagnostic challenge on the ICU].11-Month-Old Infant With Periodic Fevers, Recurrent Liver Dysfunction, and Perforin Gene Polymorphism.The limited role of interferon-γ in systemic juvenile idiopathic arthritis cannot be explained by cellular hyporesponsivenessCrohn's as an immune deficiency: from apparent paradox to evolving paradigm.Advances in understanding the pathogenesis of HLH.Macrophage activation syndrome and cytokine-directed therapies.Pathogenesis of macrophage activation syndrome and potential for cytokine- directed therapies.Elevated Granzyme B in Cytotoxic Lymphocytes is a Signature of Immune Activation in Hemophagocytic Lymphohistiocytosis.Elevation of CD16+CD56+ NK-cells and down-regulation of serum interleukin-21 (IL-21) and IL-1α after splenectomy in relapsed hemophagocytic lymphohistiocytosis of unknown cause.Laboratory parameters identify familial haemophagocytic lymphohistiocytosis from other forms of paediatric haemophagocytosis
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Inherited defects causing hemophagocytic lymphohistiocytic syndrome
description
im Dezember 2011 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 01 December 2011
@en
wetenschappelijk artikel
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наукова стаття, опублікована в грудні 2011
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name
Inherited defects causing hemophagocytic lymphohistiocytic syndrome
@en
Inherited defects causing hemophagocytic lymphohistiocytic syndrome
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type
label
Inherited defects causing hemophagocytic lymphohistiocytic syndrome
@en
Inherited defects causing hemophagocytic lymphohistiocytic syndrome
@nl
prefLabel
Inherited defects causing hemophagocytic lymphohistiocytic syndrome
@en
Inherited defects causing hemophagocytic lymphohistiocytic syndrome
@nl
P2860
P50
P1476
Inherited defects causing hemophagocytic lymphohistiocytic syndrome
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Gaël Ménasché
Geneviève de Saint Basile
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P356
10.1111/J.1749-6632.2011.06307.X
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2011-12-01T00:00:00Z