Search research articles
Contact Us
Filters
Showing results (41-50 of 130) with videos related to
Page
of 13
Sort By:
British Journal of Haematology
|
February 1, 1997
Mutations in the FVIII gene in seven families with mild haemophilia A
C Mazurier, C Gaucher, S Jorieux, et al.
Pathologie-Biologie
|
December 1, 1975
[Contribution to the isolation and study of the molecular weight of human factor VIII]
C Mazurier, A Parquet-Gernez, M Goudemand, et al.
Clinical and Laboratory Haematology
|
January 1, 1984
Cross-immunoelectrophoretic analysis of heparin and gelatin binding capacity of fibronectin
C Mazurier, A Lefevre, M P Henon, et al.
Pathologie-Biologie
|
April 1, 1977
[HLA antigen and Willebrand's disease (author's transl)]
J Goudemand, C Mazurier, A Parquet-Gernez, et al.
American Journal of Hematology
|
May 1, 1995
New variant of type II von Willebrand's disease with structural abnormality of plasma von Willebrand factor in a patient with very mild bleeding history
P Baillod, C Gaucher, B Affolter, et al.
Blood
|
May 1, 1991
The "Normandy" variant of von Willebrand disease: characterization of a point mutation in the von Willebrand factor gene
C Gaucher, S Jorieux, B Mercier, et al.
Blood
|
January 1, 1990
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, et al.
European Journal of Haematology
|
July 1, 1989
In vitro and in vivo characterization of a high-purity, solvent/detergent-treated factor VIII concentrate: evidence for its therapeutic efficacy in von Willebrand's disease
C Mazurier, C De Romeuf, A Parquet-Gernez, et al.
Thrombosis Research
|
September 15, 1984
Assay of factor IX antigen using an enzyme immuno assay
A Parquet-Gernez, C Mazurier, J Amiral, et al.
European Journal of Haematology
|
August 26, 1998
A new candidate mutation (N528S) within the von Willebrand factor propeptide identified in a Japanese patient with phenotype IIC of von Willebrand disease
C Gaucher, H Uno, T Yamazaki, et al.
Page
of 13
Search research articles
Search
Showing results (41-50 of 130) with videos related to
Sort By:
Page
of 13
British Journal of Haematology
|
February 1, 1997
Mutations in the FVIII gene in seven families with mild haemophilia A
C Mazurier, C Gaucher, S Jorieux, et al.
Pathologie-Biologie
|
December 1, 1975
[Contribution to the isolation and study of the molecular weight of human factor VIII]
C Mazurier, A Parquet-Gernez, M Goudemand, et al.
Clinical and Laboratory Haematology
|
January 1, 1984
Cross-immunoelectrophoretic analysis of heparin and gelatin binding capacity of fibronectin
C Mazurier, A Lefevre, M P Henon, et al.
Pathologie-Biologie
|
April 1, 1977
[HLA antigen and Willebrand's disease (author's transl)]
J Goudemand, C Mazurier, A Parquet-Gernez, et al.
American Journal of Hematology
|
May 1, 1995
New variant of type II von Willebrand's disease with structural abnormality of plasma von Willebrand factor in a patient with very mild bleeding history
P Baillod, C Gaucher, B Affolter, et al.
Blood
|
May 1, 1991
The "Normandy" variant of von Willebrand disease: characterization of a point mutation in the von Willebrand factor gene
C Gaucher, S Jorieux, B Mercier, et al.
Blood
|
January 1, 1990
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, et al.
European Journal of Haematology
|
July 1, 1989
In vitro and in vivo characterization of a high-purity, solvent/detergent-treated factor VIII concentrate: evidence for its therapeutic efficacy in von Willebrand's disease
C Mazurier, C De Romeuf, A Parquet-Gernez, et al.
Thrombosis Research
|
September 15, 1984
Assay of factor IX antigen using an enzyme immuno assay
A Parquet-Gernez, C Mazurier, J Amiral, et al.
European Journal of Haematology
|
August 26, 1998
A new candidate mutation (N528S) within the von Willebrand factor propeptide identified in a Japanese patient with phenotype IIC of von Willebrand disease
C Gaucher, H Uno, T Yamazaki, et al.
Page
of 13