Diagnostic importance of the two-stage factor VIII:C assay demonstrated by a case of mild haemophilia associated with His1954 → Leu substitution in the factor VIII A3 domain
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.1999.01460.x/fullpdf
Reference9 articles.
1. Familial discrepancy between the one-stage and two-stage factor VIII methods in a subgroup of patients with haemophilia A;Duncan;British Journal of Haematology,1994
2. Mutations in the FVIII gene in seven families with mild haemophilia A;Mazurier;British Journal of Haematology,1997
3. Functional and immunological assays of FVIII in 133 haemophiliacs: characterization of a subgroup of patients with mild haemophilia A and discrepancy in one- and two-stage assays;Parquet-Gernez;Thrombosis and Haemostasis,1988
4. A molecular model for the triplicated A domains of human factor VIII based on the crystal structure of human ceruloplasmin;Pemberton;Blood,1997
5. Mild hemophilia A caused by increased rate of factor VIII A2 subunit dissociation: evidence for nonproteolytic inactivation of factor VIIIa in vivo;Pipe;Blood,1999
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2. Treatment changes in hemophilia A with chromogenic factor VIII assay implementation;Research and Practice in Thrombosis and Haemostasis;2023-02
3. Insights into the Molecular Genetic of Hemophilia A and Hemophilia B: The Relevance of Genetic Testing in Routine Clinical Practice;Hämostaseologie;2022-12
4. Impact of variation in reagent combinations for one‐stage clotting assay on assay discrepancy in nonsevere haemophilia A;International Journal of Laboratory Hematology;2020-09-11
5. Genetics and Hemostatic Potential in Persons with Mild to Moderate Hemophilia A with a Discrepancy between One-Stage and Chromogenic FVIII Assays;Thrombosis and Haemostasis;2020-08-13
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