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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… Expand
National Institutes of Health

Papers overview

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Review
2016
Review
2016
Factor XIII (FXIII) is a multifunctional pro-γ-transglutaminase that, in addition to its well-known role in hemostasis, has a… Expand
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Review
2015
Review
2015
With 473 patients, Iran has about one third of the world’s patients with severe congenital factor XIII (FXIII) deficiency. A… Expand
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2012
2012
Congenital factor XIII (FXIII) deficiency is a rare, autosomal-recessive disorder, with most patients having an A-subunit (FXIII… Expand
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Review
2008
Review
2008
Inherited factor XIII (FXIII) deficiency is a rare bleeding disorder that can present with umbilical bleeding during the neonatal… Expand
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Highly Cited
2002
Highly Cited
2002
Building on a formal theory of the structural aspects of organizational change initiated in Hannan, Polos, and Carroll (2002a… Expand
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2002
2002
OBJECTIVES The objectives of this study were 1) to assess the importance of an early diagnosis for factor XIII (FXIII) deficiency… Expand
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Review
1999
Review
1999
Signs and symptoms of inherited factor XIII deficiency begin soon after birth, usually with abnormal bleeding from the umbilical… Expand
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Review
1998
Review
1998
Factor XIII deficiency is a severe autosomal recessive bleeding disorder associated with a characteristic pattern of neonatal… Expand
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Review
1996
Review
1996
Congenital factor XIII deficiency is a rare disease, but has provided valuable information on the physiological role of factor… Expand
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Highly Cited
1988
Highly Cited
1988
Factor XIII (plasma transglutaminase, fibrin stabilizing factor) is a glycoprotein that circulates in blood as a tetramer (a2b2… Expand
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