Factor XIII Deficiency

Known as: Factor XIII Deficiencies, Deficiency, factor XIII, FIBRINASE DEFICIENCY, CONGENITAL 
A deficiency of blood coagulation FACTOR XIII or fibrin stabilizing factor (FSF) that prevents blood clot formation and results in a clinical… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1967-2017
02419672017

Papers overview

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2018
2018
Factor XIII deficiency (FXIIID) is an extremely rare autosomal recessive disorder that has the highest incidence in Iran. The… (More)
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2018
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2018
Factor XIII deficiency (FXIIID) is a rare hereditary bleeding disorder arising from heterogeneous mutations, which can lead to… (More)
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2017
Review
2017
Congenital factor XIII (FXIII) deficiency is a rare, autosomal recessive bleeding disorder with potentially life-threatening… (More)
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2016
Review
2016
Factor XIII (FXIII) is a multifunctional pro-γ-transglutaminase that, in addition to its well-known role in hemostasis, has a… (More)
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2016
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2016
BACKGROUND Factor XIII (FXIII) deficiency is an extremely rare bleeding disorder with estimated incidence of one per two million… (More)
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2013
2013
Factor XIII is one of the twelve coagulation factors and also known as a fibrin-stabilizing factor. In 2012, we encountered a… (More)
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2013
Review
2013
Factor XIII (FXIII) deficiency is a rare congenital bleeding disorder. There is a paucity of data in the literature about… (More)
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2013
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2013
Congenital Factor XIII (FXIII) deficiency is a rare, inherited, autosomal recessive coagulation disorder. Most mutations of this… (More)
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2009
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2009
Factor XIII (FXIII) is a tetrameric zymogen (FXIII-A (2)B (2)) that is converted into an active transglutaminase (FXIIIa) by… (More)
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2003
2003
A defect in the factor XIII gene can result in lifelong bleeding tendency. In 3 Chinese families, hereditary coagulation factor… (More)
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