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Antithrombin III Deficiency

Known as: AT3D, Antithrombin 3 Deficiencies, Antithrombin 3 Deficiency 
A rare disorder characterized by the presence of low levels of antithrombin III which prohibits the formation of blood clots. It may be inherited… 
National Institutes of Health

Related topics

Related topics

25 relations
Antithrombin III, HumanAutosomal dominant inheritanceAutosomal recessive inheritanceBlood Coagulation Disorders

Narrower (1)

Hereditary Antithrombin Deficiency

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2010
Review
2010
Impact of Thrombophilia on Risk of Arterial Ischemic Stroke or Cerebral Sinovenous Thrombosis in Neonates and Children: A Systematic Review and Meta-Analysis of Observational Studies
Background— The aim of this study was to estimate the impact of thrombophilia on risk of first childhood stroke through a meta… 
Review
2008
Review
2008
Inherited antithrombin deficiency: a review
Summary.  Antithrombin (AT) is a potent inactivator of thrombin and factor Xa and the major inhibitor of blood coagulation… 
Highly Cited
2000
Highly Cited
2000
High levels of coagulation factor XI as a risk factor for venous thrombosis.
BACKGROUND Factor XI, a component of the intrinsic pathway of coagulation, contributes to the generation of thrombin, which is… 
Highly Cited
2000
Highly Cited
2000
Cause of portal or hepatic venous thrombosis in adults: The role of multiple concurrent factors
According to a recent hypothesis, venous thrombosis results from the concurrence of several factors. This hypothesis was assessed… 
Highly Cited
2000
Highly Cited
2000
Factor V Leiden mutation, prothrombin gene mutation, and deficiencies in coagulation inhibitors associated with Budd-Chiari syndrome and portal vein thrombosis: results of a case-control study.
In a collaborative multicenter case-control study, we investigated the effect of factor V Leiden mutation, prothrombin gene… 
Highly Cited
2000
Highly Cited
2000
Symptomatic Ischemic Stroke in Full-Term Neonates: Role of Acquired and Genetic Prothrombotic Risk Factors
Background and Purpose The present multicenter case-control study was prospectively designed to assess the extent to which single… 
Highly Cited
1996
Highly Cited
1996
Increased fetal loss in women with heritable thrombophilia
Highly Cited
1995
Highly Cited
1995
Protein C deficiency in a controlled series of unselected outpatients: an infrequent but clear risk factor for venous thrombosis (Leiden Thrombophilia Study)
A deficiency of protein C (PC), antithrombin, or protein S is strongly associated with deep-vein thrombosis in selected patients… 
Highly Cited
1974
Highly Cited
1974
Familial thrombosis due to antithrombin 3 deficiency.
A large kindred from eastern Kentucky, with extensive history of recurrent venous thrombosis and pulmonary embolism, was studied… 
Highly Cited
1965
Highly Cited
1965
Inherited Antithrombin Deficiency Causing Thrombophilia
Summary Blood coagulation systems were studied in members of a family with remarkably high incidence of thrombo - embolic… 
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