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Distinguishing between type 2B and pseudo‐von Willebrand disease and its clinical importance
British journal of haematology, 2006-06, Vol.133 (6), p.664-666
2006
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Is VWF R924Q a benign polymorphism, a marker of a null allele or a factor VIII-binding defect? The debate continues with results from the UKHCDO VWD study
Thrombosis and haemostasis, 2008-10, Vol.100 (4), p.716
2008
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The R2464C missense mutation in the von Willebrand factor gene causes a novel abnormality of multimer electrophoretic mobility and falls into the subgroup of type 2 von Willebrand disease 'unclassified'
Thrombosis and haemostasis, 2007-01, Vol.97 (1), p.159
2007
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Agarose and polyacrylamide gel electrophoresis
Methods in molecular biology (Clifton, N.J.), 2002, Vol.187, p.1
2002
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Inherited and de novo von Willebrand disease ‘Vicenza’ in UK families with the R1205H mutation: diagnostic pitfalls and new insights
British journal of haematology, 2006-10, Vol.135 (1), p.91-96
2006
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Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD)
Blood, 2007-01, Vol.109 (1), p.112-121
2007
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Aberrant dimerization of von Willebrand factor as the result of mutations in the carboxy-terminal region: identification of 3 mutations in members of 3 different families with type 2A (phenotype IID) von Willebrand disease
Blood, 2001-08, Vol.98 (3), p.674-680
2001
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An investigation of the von Willebrand factor genotype in UK patients diagnosed to have type 1 von Willebrand disease
Thrombosis and haemostasis, 2006-11, Vol.96 (5), p.630
2006
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A novel alanine or threonine 789 to proline mutation causing type 2N von Willebrand's disease when inherited homozygously or heterozygously with arginine 854 to glutamine mutation
Haemophilia : the official journal of the World Federation of Hemophilia, 2010-11, Vol.16 (6), p.966-969
2010
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short report: Distinguishing between type 2B and pseudo-von Willebrand disease and its clinical importance
British journal of haematology, 2006-06, Vol.133 (6), p.664-666
2006
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Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD). Commentary
Blood, 2007, Vol.109 (1)
2007
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Assembly of multimeric von Willebrand factor directs sorting of P-selectin
Arteriosclerosis, thrombosis, and vascular biology, 2000-07, Vol.20 (7), p.1763
2000
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