Factor VIII Binding Assay of von Willebrand Factor and the Diagnosis of Type 2N von Willebrand Disease -Results of an International Survey
- 1 January 1996
- journal article
- research article
- Published by Georg Thieme Verlag KG in Thrombosis and Haemostasis
- Vol. 76 (02) , 270-274
- https://doi.org/10.1055/s-0038-1650567
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- A novel case of compound heterozygosity with ?Normandy?/type I von Willebrand disease (vWD). Direct demonstration of the segregation of one allele with a defective expression at the mRNA level causing type I vWDHuman Genetics, 1994
- A Revised Classification of von Willebrand DiseaseThrombosis and Haemostasis, 1994
- Autosomal recessive transmission of hemophilia A due to a von Willebrand factor mutationHuman Genetics, 1993
- Recessive inheritance of von Willebrand's disease type IThe Lancet, 1993
- A single cytosine deletion in exon 18 of the von Willebrand factor gene is the most common mutation in Swedish vWD type III patientsHuman Molecular Genetics, 1992
- Further evidence for recessive inheritance of von willebrand disease with abnormal binding of von willebrand factor to factor VIIIAmerican Journal of Hematology, 1992
- Identification of two point mutations in the von Willebrand factor gene of three families with the ‘Normandy’variant of von Willebrand diseaseBritish Journal of Haematology, 1991
- Expression of von Willebrand factor "Normandy": an autosomal mutation that mimics hemophilia A.Proceedings of the National Academy of Sciences, 1991
- Evidence for a von Willebrand factor defect in factor VIII binding in three members of a family previously misdiagnosed mild haemophilia A and haemophilia A carriers: consequences for therapy and genetic counsellingBritish Journal of Haematology, 1990