Severe spontaneous arterial thrombotic manifestations in patients with inherited hypo- and afibrinogenemia
Author:
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2516.2009.01939.x/fullpdf
Reference13 articles.
1. The molecular basis of quantitative fibrinogen disorders;Asselta;J Thromb Haemost,2006
2. Incidence of bleeding symptoms in 100 patients with inherited afibrinogenemia or hypofibrinogenemia;Peyvandi;J Thromb Haemost,2006
3. Arterial and venous thrombosis in rare congenital bleeding disorders: a critical review;Girolami;Haemophilia,2006
4. Failure of DDAVP to shorten the prolonged bleeding time of two patients with congenital afibrinogenemia;Castaman;Thromb Res,1992
5. Pseudo-exon activation caused by a deep-intronic mutation in the fibrinogen γ-chain gene as a novel mechanism for congenital afibrinogenaemia;Spena;Br J Haematol,2007
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2. Congenital (hypo-)dysfibrinogenemia and bleeding: A systematic literature review;Thrombosis Research;2022-09
3. Heterogeneity of Genotype–Phenotype in Congenital Hypofibrinogenemia—A Review of Case Reports Associated with Bleeding and Thrombosis;Journal of Clinical Medicine;2022-02-18
4. Endovascular Treatment for Lower-extremity Arterial Thrombosis in a Patient with Congenital Afibrinogenemia and a History of Bleeding Complications;Internal Medicine;2022-02-01
5. Peri‐operative management of multiple tooth extractions in a patient with congenital hypofibrinogenemia receiving anticoagulant therapy;Oral Science International;2021-09-15
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