Is the assessment of von Willebrand disease prevalence an achievable challenge? The example of the French Basque Country where blood group O and factor XI deficiency are highly prevalent
Open Access
- 1 October 2004
- journal article
- Published by Elsevier in Journal of Thrombosis and Haemostasis
- Vol. 2 (10) , 1724-1726
- https://doi.org/10.1111/j.1538-7836.2004.00930.x
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Is there a ‘Basque’ profile regarding autosomal recessive deficiencies of coagulation factors?*Haemophilia, 2004
- Measurement of von Willebrand factor activity: relative effects of ABO blood type and raceJournal of Thrombosis and Haemostasis, 2003
- Von Willebrand disease type 1: a diagnosis in search of a diseaseBlood, 2003
- Guidelines for the diagnosis and management of von Willebrand disease in ItalyHaemophilia, 2002
- Factor XI deficiency in French Basques is caused predominantly by an ancestral Cys38Arg mutation in the factor XI geneBlood, 2002
- Congenital von Willebrand disease type 1: definition, phenotypes, clinical and laboratory assessmentBest Practice & Research Clinical Haematology, 2001
- Identification of Type 2 von Willebrand Disease in Previously Diagnosed Type 1 Patients: a Reappraisal Using Phenotypes, Genotypes and Molecular ModellingThrombosis and Haemostasis, 2000
- Impact, Diagnosis and Treatment of von Willebrand DiseaseThrombosis and Haemostasis, 2000
- The effect of ABO blood group on the diagnosis of von Willebrand diseaseBlood, 1987