Fibrinogen Milano II: A Congenital Dysfibrinogenaemia Associated with Juvenile Arterial and Venous Thrombosis
Author:
Affiliation:
1. The TNO Gaubius Institute for Cardiovascular Research, Leiden, The Netherlands
2. The A. Bianchi Bonomi Hemophilia and Thrombosis Centre and Institute of Internal Medicine, University of Milan, Italy
Abstract
Publisher
Georg Thieme Verlag KG
Subject
Hematology
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0038-1661463.pdf
Cited by 24 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Fibrinogen BOE II: dysfibrinogenemia with bleeding and defective thrombin binding;Research and Practice in Thrombosis and Haemostasis;2023-07
2. Fibrin monomers derived from thrombogenic dysfibrinogenemia, Naples-type variant (BβAla68Thr), showed almost entirely normal polymerization;Thrombosis Research;2018-12
3. A novel mutation in exon 2 of FGB caused by c.221G>T † substitution, predicting the replacement of the native Arginine at position 74 with a Leucine (p.Arg74Leu † ) in a proband from a Kurdish family with dysfibrinogenaemia and familial venous and arterial thrombosis;Journal of Thrombosis and Thrombolysis;2016-11-03
4. Clinical features and molecular basis of 102 Chinese patients with congenital dysfibrinogenemia;Blood Cells, Molecules, and Diseases;2015-12
5. Hereditary Disorders of Fibrinogen;Annals of the New York Academy of Sciences;2006-01-25
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