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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… Expand
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2015
2015
Cytotoxic T‐lymphocytes (CTL) kill their targets by cytolytic granule secretion at the immunological synapse. The Sec/Munc… Expand
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2015
2015
Cytotoxic lymphocytes encompass natural killer (NK) cells and cytotoxic T lymphocytes (CTL). These cells detect and kill virus… Expand
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2014
2014
Familial hemophagocytic lymphohistiocytosis (FHL) is an often-fatal hyperinflammatory disorder caused by autosomal recessive… Expand
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Review
2014
Review
2014
I n 1952, Dr James Farquhar, a Scottish pediatrician noticed the familial recurrence of a disease affecting male and female… Expand
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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… Expand
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2011
2011
Familial hemophagocytic lymphohistiocytosis (FHL) is typically an autosomal recessive, early‐onset, life‐threatening immune… Expand
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Review
2010
Review
2010
Hemophagocytic lymphohistiocytosis (HLH) is a potentially fatal immune disorder characterized by uncontrolled lymphocyte- and… Expand
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Highly Cited
2007
Highly Cited
2007
Familial hemophagocytic lymphohistiocytosis (FHL) is typically an early onset, fatal disease characterized by a sepsislike… Expand
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1999
1999
We have determined the sequence of a novel LIM protein, termed FHL4. It was found to contain the defining secondary structural… Expand
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