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hematology, hemophagocytic lymphohistiocytosis (HLH), also known as haemophagocytic lymphohistiocytosis (British spelling), and hemophagocytic or haemophagocytic...

storm syndromes include familial hemophagocytic lymphohistiocytosis, Epstein-Barr virus–associated hemophagocytic lymphohistiocytosis, systemic or non-systemic...

autoimmune thrombocytopenia, and autoimmune thyroid disease. Familial hemophagocytic lymphohistiocytosis, an autosomal recessive primary immunodeficiency, is...

lymphocytes with compensatory macrophage activation (Familial hemophagocytic lymphohistiocytosis (HLH)) Inactivation of IL‑10 signaling (Early-onset enterocolitis)...

sources recommend classifying this condition as "X-linked familial hemophagocytic lymphohistiocytosis" instead of X-linked lymphoproliferative disease. Mutations...

recessive immunoregulatory disorder in infants, known as familial hemophagocytic lymphohistiocytosis (FHL), typically appearing before 12 months of age. This...

autoimmune thrombocytopenia and autoimmune thyroid disease. Familial hemophagocytic lymphohistiocytosis, an autosomal recessive primary immunodeficiency, is...

syndrome systemic lupus erythematosus serum sickness familial hemophagocytic lymphohistiocytosis autoimmune hemolytic anemia autoimmune lymphoproliferative...

following groups:: 714–724  X-type histiocytoses Non-X histiocytoses Lymphohistiocytosis is a similar immune system disease characterized by the inappropriate...

loss of perforin function leads to a syndrome called familial hemophagocytic lymphohistiocytosis […]”. This syndrome can lead to death because both T...

(2006). "Analysis of natural killer-cell function in familial hemophagocytic lymphohistiocytosis (FHL): defective CD107a surface expression heralds Munc13-4...

Chédiak–Higashi syndrome, Griscelli syndrome type 2 Familial hemophagocytic lymphohistiocytosis: perforin deficiency, UNC13D deficiency, syntaxin 11...

refer to: Fachhochschule Lübeck, a German university Familial hemophagocytic lymphohistiocytosis Family History Library, a genealogical research facility...

in hemophagocytic lymphohistiocytosis (HLH) there is marked inappropriate and ineffective T cell activation that leads to an increased hemophagocytic activity...

"Sequence analysis of the granulysin and granzyme B genes in familial hemophagocytic lymphohistiocytosis". Human Genetics. 112 (1): 98–99. doi:10.1007/s00439-002-0841-0...

Perforin deficiency results in the commonly fatal disorder familial hemophagocytic lymphohistiocytosis (FHL or HLH). This disease is characterised by an overactivation...

lethal genital anomalies Hemolytic-uremic syndrome Hemophagocytic lymphohistiocytosis Hemophagocytic reticulosis Hemophilia A Hemophilic arthropathy Hemophobia...

STX11 has been shown to interact with SNAP25 and SNAP23. Hemophagocytic lymphohistiocytosis Peutz–Jeghers syndrome GRCh38: Ensembl release 89: ENSG00000135604...

directed at the specific features of each type of complication. Hemophagocytic lymphohistiocytosis (HLH) is a rare disorder characterized by a systemic inflammatory...

diseases, differentiation syndrome, engraftment syndrome, hemophagocytic lymphohistiocytosis, the ovarian hyperstimulation syndrome, viral hemorrhagic...