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Journal Articles

A Novel Mutation in the D3 Domain of von Willebrand Factor Markedly Decreases Its Ability to Bind Factor VIII and Affects Its Multimerization

S. Jorieux, C. Gaucher, J. Goudemand, C. Mazurier

Blood (1998) 92 (12): 4663–4670.

https://doi.org/10.1182/blood.V92.12.4663

Published: 1998

Journal Articles

A Patient With Type 2N von Willebrand Disease Is Heterozygous for a New Mutation: Gly22Glu. Demonstration of a Defective Expression of the Second Allele by the Use of Monoclonal Antibodies

J. Gu, S. Jorieux, J.M. Lavergne, C. Ruan, C. Mazurier, D. Meyer

Blood (1997) 89 (9): 3263–3269.

https://doi.org/10.1182/blood.V89.9.3263

Published: 1997

Journal Articles

The mutation Arg (53)----Trp causes von Willebrand disease Normandy by abolishing binding to factor VIII. Studies with recombinant von Willebrand factor

S Jorieux, EA Tuley, C Gaucher, C Mazurier, JE Sadler

Blood (1992) 79 (3): 563–567.

https://doi.org/10.1182/blood.V79.3.563.563

Published: 1992

Journal Articles

The "Normandy" variant of von Willebrand disease: characterization of a point mutation in the von Willebrand factor gene

C Gaucher, S Jorieux, B Mercier, D Oufkir, C Mazurier

Blood (1991) 77 (9): 1937–1941.

https://doi.org/10.1182/blood.V77.9.1937.1937

Published: 1991

Journal Articles

A new von Willebrand factor (vWF) defect in a patient with factor VIII (FVIII) deficiency but with normal levels and multimeric patterns of both plasma and platelet vWF. Characterization of abnormal vWF/FVIII interaction

C Mazurier, J Dieval, S Jorieux, J Delobel, M Goudemand

Blood (1990) 75 (1): 20–26.

https://doi.org/10.1182/blood.V75.1.20.20

Published: 1990

NARROW

A Novel Mutation in the D3 Domain of von Willebrand Factor Markedly Decreases Its Ability to Bind Factor VIII and Affects Its Multimerization

A Patient With Type 2N von Willebrand Disease Is Heterozygous for a New Mutation: Gly22Glu. Demonstration of a Defective Expression of the Second Allele by the Use of Monoclonal Antibodies

The mutation Arg (53)----Trp causes von Willebrand disease Normandy by abolishing binding to factor VIII. Studies with recombinant von Willebrand factor

The "Normandy" variant of von Willebrand disease: characterization of a point mutation in the von Willebrand factor gene

A new von Willebrand factor (vWF) defect in a patient with factor VIII (FVIII) deficiency but with normal levels and multimeric patterns of both plasma and platelet vWF. Characterization of abnormal vWF/FVIII interaction

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ASH Publications

American Society of Hematology

A Novel Mutation in the D3 Domain of von Willebrand Factor Markedly Decreases Its Ability to Bind Factor VIII and Affects Its Multimerization

A Patient With Type 2N von Willebrand Disease Is Heterozygous for a New Mutation: Gly22Glu. Demonstration of a Defective Expression of the Second Allele by the Use of Monoclonal Antibodies

The mutation Arg (53)----Trp causes von Willebrand disease Normandy by abolishing binding to factor VIII. Studies with recombinant von Willebrand factor

The "Normandy" variant of von Willebrand disease: characterization of a point mutation in the von Willebrand factor gene

A new von Willebrand factor (vWF) defect in a patient with factor VIII (FVIII) deficiency but with normal levels and multimeric patterns of both plasma and platelet vWF. Characterization of abnormal vWF/FVIII interaction

Email alerts

ASH Publications

American Society of Hematology

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