Congenital antithrombin III deficiency
- 1 September 1989
- journal article
- review article
- Published by Elsevier in American Journal Of Medicine
- Vol. 87 (3), S34-S38
- https://doi.org/10.1016/0002-9343(89)80529-7
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- The Frequency of Type I Heterozygous Protein S and Protein C Deficiency in 141 Unrelated Young Patients with Venous ThrombosisThrombosis and Haemostasis, 1988
- Prevalence of protein C (PC) and protein S (PS) deficiency in patients with thrombotic diseaseThrombosis Research, 1986
- Associated von Willebrand disease as a possible cause of lack of thrombosis in an AT III abnormality (AT III Trento)Blut: Zeitschrift für die Gesamte Blutforschung, 1986
- Congenital protein C deficiency and thrombotic disease in nine French families.BMJ, 1984
- Antithrombin III toyama: A hereditary abnormal antithrombin III of a patient with recurrent thrombophlebitisThrombosis Research, 1983
- Antithrombin III Deficiency and ThromboembolismClinics in Haematology, 1981
- Maternal and fetal sequelae of anticoagulation during pregnancyAmerican Journal Of Medicine, 1980
- HEPARIN-INDUCED DECREASE IN CIRCULATING ANTITHROMBIN-IIIThe Lancet, 1977
- Actions and Interactions of Antithrombin and HeparinNew England Journal of Medicine, 1975
- Inherited Antithrombin Deficiency Causing ThrombophiliaThrombosis and Haemostasis, 1965