Challenges in defining type 2M von Willebrand disease: results from a Canadian cohort study
Open Access
- 26 June 2007
- journal article
- Published by Elsevier BV in Journal of Thrombosis and Haemostasis
- Vol. 5 (9), 1914-1922
- https://doi.org/10.1111/j.1538-7836.2007.02666.x
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Assay of the von Willebrand factor (VWF) propeptide to identify patients with type 1 von Willebrand disease with decreased VWF survivalPublished by American Society of Hematology ,2006
- Diagnosis of Inherited von Willebrand Disease: A Clinical PerspectiveSeminars in Thrombosis and Hemostasis, 2006
- The mutational spectrum of type 1 von Willebrand disease: results from a Canadian cohort studyBlood, 2006
- Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian Type 1 VWD StudyJournal of Thrombosis and Haemostasis, 2006
- An investigation of the von Willebrand factor genotype in UK patients diagnosed to have type 1 von Willebrand diseaseThrombosis and Haemostasis, 2006
- Biologic response to desmopressin in patients with severe type 1 and type 2 von Willebrand disease: results of a multicenter European studyBlood, 2004
- A molecular approach to the classification of von Willebrand diseaseBest Practice & Research Clinical Haematology, 2001
- The arginine-552-cysteine (R1315C) mutation within the A1 loop of von Willebrand factor induces an abnormal folding with a loss of function resulting in type 2A–like phenotype of von Willebrand disease: study of 10 patients and mutated recombinant von Willebrand factorBlood, 2001
- Prevalence of von Willebrand disease in children: A multiethnic studyThe Journal of Pediatrics, 1993
- Human von Willebrand Factor (vWF): Isolation of Complementary DNA (cDNA) Clones and Chromosomal LocalizationScience, 1985