Congenital Thrombotic Thrombocytopenic Purpura

Known as: Syndrome, Schulman-Upshaw, Microangiopathic Hemolytic Anemia, Congenital, Schulman-Upshaw Syndrome 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1985-2016
0519852016

Papers overview

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2014
2014
Upshaw-Schulman syndrome (USS) is due to severe congenital deficiency of von Willebrand factor (VWF)-cleaving protease ADAMTS13… (More)
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2014
2014
Congenital thrombotic thrombocytopenic purpura (TTP) is an inherited disease caused by mutations in the ADAMTS 13 gene and has… (More)
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2013
2013
Congenital thrombotic thrombocytopenic purpura (cTTP) is a rare, recessively inherited genetic disorder with varying clinical… (More)
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2012
2012
Congenital thrombotic thrombocytopenic purpura (cTTP) is a rare disorder of childhood that has clinical and laboratory… (More)
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2007
2007
ADAMTS13 mutations S203P, R268P, R507Q and A596V were previously identified in French patients with hereditary thrombotic… (More)
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2006
2006
This report presents seven children with congenital thrombotic thrombocytopenic purpura (TTP). Six had a history of severe… (More)
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2005
2005
Severe ADAMTS13 deficiency in thrombotic thrombocytopenic purpura (TTP) is either constitutional and caused by ADAMTS13 mutations… (More)
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2004
2004
Congenital thrombotic thrombocytopenic purpura (TTP) is an inherited form of TTP due to the deficiency of von Willebrand factor… (More)
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2004
2004
Congenital thrombotic thrombocytopenic purpura/hemolytic uremic syndrome (TTP/HUS) is associated with an inherited von Willebrand… (More)
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2002
2002
There is increasing evidence that congenital thrombotic thrombocytopenic purpura (TTP) is caused by an absolute deficiency of von… (More)
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