von Willebrand disease: advances in pathogenetic understanding, diagnosis, and therapy
Published 2013 View Full Article
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Title
von Willebrand disease: advances in pathogenetic understanding, diagnosis, and therapy
Authors
Keywords
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Journal
BLOOD
Volume 122, Issue 23, Pages 3735-3740
Publisher
American Society of Hematology
Online
2013-09-25
DOI
10.1182/blood-2013-06-498303
References
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Related references
Note: Only part of the references are listed.- No increase in bleeding identified in type 1 VWD subjects with D1472H sequence variation
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- (2012) V. H. FLOOD et al. JOURNAL OF THROMBOSIS AND HAEMOSTASIS
- Use of a mouse model to elucidate the phenotypic effects of the von Willebrand factor cleavage mutants, Y1605A/M1606A and R1597W
- (2012) C. M. PRUSS et al. JOURNAL OF THROMBOSIS AND HAEMOSTASIS
- Comparison of type I, type III and type VI collagen binding assays in diagnosis of von Willebrand disease
- (2012) V. H. FLOOD et al. JOURNAL OF THROMBOSIS AND HAEMOSTASIS
- VWF mutations and new sequence variations identified in healthy controls are more frequent in the African-American population
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- How I treat von Willebrand disease
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- Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM-1VWD study
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- The prevalence of symptomatic von Willebrand disease in primary care practice
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- Identification of type 1 von Willebrand disease patients with reduced von Willebrand factor survival by assay of the VWF propeptide in the European study: Molecular and Clinical Markers for the Diagnosis and Management of Type 1 VWD (MCMDM-1VWD)
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- (2008) A. B. Federici et al. BLOOD
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