Comparing bleed frequency and factor concentrate use between haemophilia A and B patients
Author:
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2516.2011.02506.x/fullpdf
Reference7 articles.
1. Comparison of the rates of joint arthroplasty in patients with severe factor VIII and IX deficiency: an index of different clinical severity of the 2 coagulation disorders;Tagariello;Blood,2009
2. Less severe bleeding in haemophilia B than in haemophilia A;Lowe;J Thromb Haemost,2008
3. Validation of a composite score for clinical severity of haemophilia;Schulman;J Thromb Haemost,2008
4. Evaluation of thrombin generating capacity in plasma from patients with haemophilia A and B;Dargaud;Thromb Haemost,2005
5. Thromboelastography in children with coagulation factor deficiencies;Chitlur;Br J Haematol,2008
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1. Relationship between plasma tissue Factor Pathway Inhibitor (TFPI) levels, thrombin generation and clinical risk of bleeding in patients with severe haemophilia A or B;Haemophilia;2024-04-22
2. A post hoc comparative real‐world analysis of HEAD‐US score for joint health assessment of patients with severe haemophilia A and B in Spain;Haemophilia;2024-01-28
3. Intramural Hematoma of Gastrointestinal Tract in People with Hemophilia A and B;Journal of Clinical Medicine;2023-04-24
4. Osteoporosis in hemophilia: what is its importance in clinical practice?;Expert Review of Hematology;2022-08-03
5. Applicability of the Thrombin Generation Test to Evaluate the Hemostatic Status of Hemophilia A Patients in Daily Clinical Practice;Journal of Clinical Medicine;2022-06-10
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