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Hemophagocytic lymphohistiocytosis, familial, 4

Known as: FHL4, HLH4, HPLH4 
National Institutes of Health

Papers overview

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2017
2017
Dear Editor, Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening hyperinflammatory disorder that is characterized by… 
2015
2015
Cytotoxic T‐lymphocytes (CTL) kill their targets by cytolytic granule secretion at the immunological synapse. The Sec/Munc… 
2014
2014
Familial hemophagocytic lymphohistiocytosis (FHL) is an often-fatal hyperinflammatory disorder caused by autosomal recessive… 
Highly Cited
2012
Highly Cited
2012
The platelet release reaction plays a critical role in thrombosis and contributes to the events that follow hemostasis. Previous… 
2011
2011
Familial hemophagocytic lymphohistiocytosis (FHL) is typically an autosomal recessive, early‐onset, life‐threatening immune… 
Review
2010
Review
2010
Familial haemophagocytic lymphohistiocytosis (FHL) is a rare disease of uncontrolled inflammation. Patients typically present… 
Review
2010
Review
2010
Hemophagocytic lymphohistiocytosis (HLH) is a potentially fatal immune disorder characterized by uncontrolled lymphocyte- and… 
Highly Cited
2007
Highly Cited
2007
Familial hemophagocytic lymphohistiocytosis (FHL) is typically an early onset, fatal disease characterized by a sepsislike… 
Review
2005
Review
2005
Abstract.Numerous cellular processes require the concerted action of multiple proteins that assemble in functional complexes… 
1999
1999
We have determined the sequence of a novel LIM protein, termed FHL4. It was found to contain the defining secondary structural…