Ongoing risk of thrombosis with factor XI concentrate: 5 years experience in two centres
Author:
Affiliation:
1. St George's University Hospitals NHS Foundation Trust; London UK
2. Barts and The London School of Medicine & Dentistry; The Royal London Hospital; QMUL; London UK
3. The Royal London Hospital; Barts Health NHS Trust; London UK
Publisher
Wiley
Subject
Genetics (clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/hae.12682/fullpdf
Reference28 articles.
1. United Kingdom Haemophilia Centres Doctors’ Organisation Bleeding disorder statistics for April 2011 to March 2012 2012 1 87
2. Variable bleeding manifestations characterize different types of surgery in patients with severe factor XI deficiency enabling parsimonious use of replacement therapy;Salomon;Haemophilia,2006
3. The rare coagulation disorders-review with guidelines for management from the United Kingdom Haemophilia Centre Doctors’ Organisation;Bolton-Maggs;Haemophilia,2004
4. Factor XI deficiency;Gomez;Haemophilia,2008
5. Classification of rare bleeding disorders (RBDs) based on the association between coagulant factor activity and clinical bleeding severity;Peyvandi;J Thromb Haemost,2012
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