Familial Functional Antithrombin III Deficiency
- 24 April 1980
- journal article
- research article
- Published by Wiley in Scandinavian Journal of Haematology
- Vol. 24 (2) , 105-109
- https://doi.org/10.1111/j.1600-0609.1980.tb02352.x
Abstract
A family with a tendency to thrombosis and decreased antithrombin III (AT III) activity in plasma, but normal immunoreactive AT III is reported. 7 members of the family had the AT III defect, 4 of whom have had thrombotic episodes. The importance of biological determination of AT III when studying patients with recurrent thrombotic episodes is emphasized.Keywords
This publication has 17 references indexed in Scilit:
- SUBCUTANEOUS HEPARIN FOR THROMBOSIS IN PREGNANT WOMEN WITH HEREDITARY ANTITHROMBIN DEFICIENCYThe Lancet, 1979
- ANTITHROMBIN III AND HEPARINBritish Medical Bulletin, 1978
- Familial Antithrombin III Deficiency as Pathogenesis of Deep Venous ThrombosisActa Medica Scandinavica, 1978
- Antithrombin (heparin cofactor) assay with “new” chromogenic substrates (S-2238 and Chromozym TH)Thrombosis Research, 1977
- Antifactor Xa Activity in Thrombophilia Studies in a Family with At-III DeficiencyScandinavian Journal of Haematology, 1977
- Hereditary antithrombin III deficiencyThe American Journal of Medicine, 1976
- Hereditary antithrombin iii deficiency and thromboembolic diseaseAmerican Journal of Hematology, 1976
- Inherited Antithrombin-III Deficiency Causing Mesenteric Venous InfarctionAnnals of Surgery, 1975
- The assay of antithrombin using a synthetic chromogenic substrate for thrombinThrombosis Research, 1974
- Aggregation of Blood Platelets by Adenosine Diphosphate and its ReversalNature, 1962