Associated von Willebrand disease as a possible cause of lack of thrombosis in an AT III abnormality (AT III Trento)-Reference-Cited by-同舟云学术

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Associated von Willebrand disease as a possible cause of lack of thrombosis in an AT III abnormality (AT III Trento)

Published:1986-01 Issue:1 Volume:52 Page:29-33
ISSN:0006-5242
Container-title:Blut
language:en
Short-container-title:Blut

Author:

Girolami A.,Cappellato M. G.,Vicarioto M. A.,Casonato S.,Marafioti F.

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine,Hematology

Link

http://link.springer.com/content/pdf/10.1007/BF00320139.pdf

Reference26 articles.

1. Abildgaard U, Lie M, �degard OR (1977) Antithrombin (heparin cofactor) assay with ?new? chromogenic substrates (S-2238 and Chromozym-TH). Thromb Res 11: 549

2. Blomb�ck M, Blomb�ck B, Olsson P, Svendsen L (1974) The assay of antithrombin using a synthetic chromogenic substrate for thrombin. Thromb Res 5: 621

3. Clarke HGM, Freeman T (1968) Quantitative immunoelectrophoresis of human serum protein. Clin Sci 35: 403

4. Egeberg O (1965) Inherited antithrombin deficiency causing thrombophilia. Thromb Diath Haemorrh 13: 516

5. Girolami A, Venturelli P, Cella G, Virgolini L, Burul A (1976) Combined hereditary deficiency of factor VII and factor VIII. A distinct coagulation disorder due to the lack of an autosomal gene controlling factor VII and VIII activation. Acta Haematol 35: 181?191

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1. Von Willebrand factor and thrombosis;Annals of Hematology;2006-03-28

2. Thrombotic complications in von Willebrand disease;Hematology;2006-02

3. Antithrombin Abnormalities and Perinatal Management;Current Drug Targets;2005-08-01

4. Familial Association of Hypoplasminogenemia and Heterozygous Factor V Deficiency;Clinical and Applied Thrombosis/Hemostasis;1999-10

5. Familial Thrombophilia: A Review Analysis;Clinical and Applied Thrombosis/Hemostasis;1996-10

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