Author:
Kalina Uwe,Stöhr Hans-Arnold,Bickhard Heike,Knaub Sigurd,Siboni Simona M,Mannucci Pier M,Peyvandi Flora
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Hematology,General Medicine
Reference35 articles.
1. Rare bleeding disorder registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias;Acharya;J Thromb Haemost,2004
2. Incidence of bleeding symptoms in 100 patients with inherited afibrinogenemia or hypofibrinogenemia;Peyvandi;J Thromb Haemost,2006
3. Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group;Santacroce;Blood Coagul Fibrinolysis,2006
4. Mutational screening of six afibrinogenemic patients: identification and characterization of four novel molecular defects;Monaldini;Thromb Haemost,2007
5. The rare coagulation disorders: review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation;Bolton-Maggs;Haemophilia,2004
Cited by
73 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