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Title
Translational medicine advances in von Willebrand disease
Authors
Keywords
-
Journal
JOURNAL OF THROMBOSIS AND HAEMOSTASIS
Volume 11, Issue -, Pages 75-83
Publisher
Wiley
Online
2013-07-01
DOI
10.1111/jth.12257
References
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Related references
Note: Only part of the references are listed.- Alloantibodies in von Willebrand disease
- (2013) P. D. James et al. BLOOD
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- (2012) Y.-F. Zhou et al. BLOOD
- Critical von Willebrand factor A1 domain residues influence type VI collagen binding
- (2012) V. H. FLOOD et al. JOURNAL OF THROMBOSIS AND HAEMOSTASIS
- von Willebrand factor: the old, the new and the unknown
- (2012) P. J. LENTING et al. JOURNAL OF THROMBOSIS AND HAEMOSTASIS
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- (2012) V. H. FLOOD et al. JOURNAL OF THROMBOSIS AND HAEMOSTASIS
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- (2012) Q. Y. Wang et al. JOURNAL OF THROMBOSIS AND HAEMOSTASIS
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- (2011) Wayne L. Chandler et al. AMERICAN JOURNAL OF CLINICAL PATHOLOGY
- VWF mutations and new sequence variations identified in healthy controls are more frequent in the African-American population
- (2011) D. B. Bellissimo et al. BLOOD
- Surveillance of female patients with inherited bleeding disorders in United States Haemophilia Treatment Centres
- (2011) V. R. BYAMS et al. HAEMOPHILIA
- Absent collagen binding in a VWF A3 domain mutant: utility of the VWF:CB in diagnosis of VWD
- (2010) V. H. FLOOD et al. JOURNAL OF THROMBOSIS AND HAEMOSTASIS
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- (2010) Peter Turecek et al. SEMINARS IN THROMBOSIS AND HEMOSTASIS
- Characterization of W1745C and S1783A: 2 novel mutations causing defective collagen binding in the A3 domain of von Willebrand factor
- (2009) A. F. Riddell et al. BLOOD
- von Willebrand factor to the rescue
- (2009) S. F. De Meyer et al. BLOOD
- The mutation spectrum associated with type 3 von Willebrand disease in a cohort of patients from the North West of England
- (2009) M. S. SUTHERLAND et al. HAEMOPHILIA
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- (2009) I. R. PEAKE et al. JOURNAL OF THROMBOSIS AND HAEMOSTASIS
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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)
- (2008) S. L. Haberichter et al. BLOOD
- Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): results from the European Study MCMDM-1VWD
- (2008) G. Castaman et al. BLOOD
- Clinical and molecular predictors of thrombocytopenia and risk of bleeding in patients with von Willebrand disease type 2B: a cohort study of 67 patients
- (2008) A. B. Federici et al. BLOOD
- The molecular analysis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors’ Organisation Haemophilia Genetics Laboratory Network
- (2008) S. KEENEY et al. HAEMOPHILIA
- Expression studies of missense mutations p.D141Y, p.C275S located in the propeptide of von Willebrand factor in patients with type 3 von Willebrand disease
- (2008) L. BARONCIANI et al. HAEMOPHILIA
- von Willebrand disease (VWD): evidence-based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA)
- (2008) W. L. NICHOLS et al. HAEMOPHILIA
- Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM-1VWD)
- (2008) U. BUDDE et al. JOURNAL OF THROMBOSIS AND HAEMOSTASIS
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