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- Alpha-2-macroglobulin may provide protection from thromboembolic events in antithrombin III-deficient children Academic Article
- An Antithrombin III Assay Based on Factor Xa Inhibition Provides a More Reliable Test to Identify Congenital Antithrombin III Deficiency Than an Assay Based on Thrombin Inhibition Academic Article
- An overview of the mechanism of action of antithrombin and its inherited deficiency states Academic Article
- Antithrombin III mutation database: first update. For the Thrombin and its Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Academic Article
- Congenital antithrombin III deficiency Academic Article
- Increased fetal loss in women with heritable thrombophilia Academic Article
- Inherited Thrombophilia in Ischemic Stroke and Its Pathogenic Subtypes Academic Article
- Management of anti-thrombin III deficiency during pregnancy without administration of anti-thrombin III Academic Article
- Management of hereditary antithrombin deficiency in pregnancy Academic Article
- Measurement of Markers of Activated Coagulation in Antithrombin III Deficient Subjects Academic Article
- Molecular structural analysis of a novel and de-novo mutation in theSERPINC1gene associated with type 1 antithrombin deficiency Academic Article
- Partial deletion of an antithrombin III allele in a kindred with a type 1 deficiency. Academic Article
- Targeted mutagenesis of zebrafish antithrombin III triggers disseminated intravascular coagulation and thrombosis, revealing insight into function Academic Article
- The Molecular Pathology of Inherited Human Antithrombin III Deficiency Academic Article
- Thrombosis in Antithrombin-III Deficiency Academic Article
- Thrombosis in Antithrombin-III-deficient Persons Academic Article
- Treatment of Venous Thromboembolism in Patients with Congenital Deficiency of Antithrombin III Academic Article
- Venous Thromboembolism, Thrombophilia, Antithrombotic Therapy, and Pregnancy Academic Article
- c.1058C>T variant in theSERPINC1gene is pathogenic for antithrombin deficiency Academic Article