Déficit homozygote en antithrombine de type II HBS (99Leu-Phe) : une cause rare de thromboses artérielles récidivantes
Author:
Publisher
Elsevier BV
Subject
Gastroenterology,Internal Medicine
Reference12 articles.
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3. Homozygous antithrombin defiency type II (99 Leu to Phe Mutation) and childhood thromboembolism;Kuhle;Thromb Haemost,2001
4. Homozygous antithrombin deficiency: report of two new cases (99 Leu to Phe) associated with arterial and venous thrombosis;Chowdhury;Thromb Haemost,1994
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1. Management and outcome of pregnancies in women with antithrombin deficiency;Blood Coagulation & Fibrinolysis;2015-10
2. A new case of successful outcome of pregnancy in a carrier of homozygous type II (L99F) antithrombin deficiency;Blood Coagulation & Fibrinolysis;2014-01
3. Molecular basis and thrombotic manifestations of antithrombin deficiency in 15 unrelated Chinese patients;Thrombosis Research;2013-09
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