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Thromb Haemost 1987; 57(01): 123
DOI: 10.1055/s-0038-1651076
DOI: 10.1055/s-0038-1651076
Letters to the Editor
The Incidence of Thrombotic Manifestations in AT III Abnormalities
Further Information
Publication History
Received 10 July 1986
Accepted after revision 01 October 1986
Publication Date:
06 July 2018 (online)
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References
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- 3 Fischer AM, Gazengel C, Dautzenberg MD, Benhammo J, Beguin S, Vergoz D. A new case of abnormal antithrombin III (AT III): biological characteristics and thromboembolic accidents management. Thromb Haemostas 1983; 50: 358 (Abstr)
- 4 Fischer AM, Cornu P, Sternberg C, Meriane F, Chafa O, Dautzenberg MD, Beguin S, Desnos M. Antithrombin III Alger: a new homozygous AT III variant. Thromb Haemostas 1986; 55: 218-221
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- 6 Girolami A, Cappellato G, Vicarioto MA, Vergolani A, Traverso R. Behavior of antithrombin III abnormalities in the crossed immunoelectrophoretic system. Folia Haematol 1985; 112: 159-164
- 7 Girolami A, Fabris F, Cappellato G, Sainati L, Boeri G. Antithrombin III Padua2: a new congenital abnormality with defective heparin co-factor activities but no thrombotic disease. Blut 1983; 47: 93-103
- 8 Girolami A, Marafioti F, Rubestello M, Vicarioto MA, Cappellato G, Maruccolo M. Antithrombin III Trento: a new congenital AT III abnormality with a peculiar crossed immunoelectrophoretic pattern in the absence of heparin. Acta Haematol 1984; 72: 73-82
- 9 Girolami A, Cappellato G, Vicarioto MA, Casonato S, Marafioti F. Associated von Willebrand’s disease as a possible cause of lack of thrombosis in AT III (AT III Trento). Blut 1986; 52: 29-33
- 10 Howarth DJ, Samson D, Stirling Y, Seghatchian MJ. Antithrombin III “Northwick Park”: a variant antithrombin with normal affinity for heparin but reduced heparin co-factor activity. Thromb Haemostas 1985; 53: 314-319
- 11 Koide T, Takahashi K, Odami S, Ono T, Sakuragawa N. Isolation and characterization of a hereditary abnormal antithrombin III “antithrombin III Toyama”. Thromb Res 1983; 31: 319-328
- 12 Nagy I, Losonczy H. Three types of hereditary AT III deficiency. Thromb Haemostas 1979; 42: 187 (Abstr)
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- 14 Tran TH, Bounameaux H, Bondeli C, Honkanen H, Marbet GA, Duckert F. Purification and partial characterization of a hereditary abnormal antithrombin III fraction of a patient with recurrent thrombophlebitis. Thromb Haemostas 1980; 44: 87-91
- 15 Wolf M, Boyer C, Lavergne JM, Larrieu MJ. A new familial variant of Antithrombin III: Antithrombin III Paris. Br J Haematol 1982; 51: 285-295