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C Mazurier

Showing results (81-90 of 130) with videos related to

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Critical Care Medicine|December 1, 1986
Plasma fibronectin in severe infectious purpura of childrenF Leclerc, A Martinot, R Beuscart, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 1, 1997
Evaluation of a new automated ELISA test for von Willebrand factor using two monoclonal antibodiesJ L Pittet, V Barbalat, M Sanvert, et al.
British Journal of Haematology|December 19, 1998
Identification of new type 2B von Willebrand disease mutations: Arg543Gln, Arg545Pro and Arg578LeuL Hilbert, C Gaucher, J F Abgrall, et al.
Blood|May 1, 1997
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 antibodiesJ Gu, S Jorieux, J M Lavergne, et al.
Thrombosis and Haemostasis|April 1, 1995
Diagnosis of subtype 2B von Willebrand disease in a patient with 2A phenotype of plasma von Willebrand factorC Gaucher, C de Romeuf, M Rauïs-Morret, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|October 1, 1990
Expression in Escherichia coli of a recombinant fragment (Ile 914-Leu 1364) of human von Willebrand factor containing a collagen binding domainS Jorieux, G Piétu, C Gaucher, et al.
Best Practice & Research. Clinical Haematology|November 1, 2001
Type 2 von Willebrand disease causing defective von Willebrand factor-dependent platelet functionD Meyer, E Fressinaud, L Hilbert, et al.
British Journal of Haematology|February 1, 1992
Clinical and biological evaluation in von Willebrand's disease of a von Willebrand factor concentrate with low factor VIII activityJ Goudemand, C Mazurier, A Marey, et al.
Blood|March 15, 1994
Leu 697-->Val mutation in mature von Willebrand factor is responsible for type IIB von Willebrand diseaseL Hilbert, C Gaucher, C de Romeuf, et al.
British Journal of Haematology|October 29, 1998
Type 2N von Willebrand disease due to Arg91Gln substitution and a cytosine deletion in exon 18 of the von Willebrand factor geneA Casonato, C Gaucher, E Pontara, et al.
Pageof 13

Showing results (81-90 of 130) with videos related to

Sort By:
Pageof 13
Critical Care Medicine|December 1, 1986
Plasma fibronectin in severe infectious purpura of childrenF Leclerc, A Martinot, R Beuscart, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 1, 1997
Evaluation of a new automated ELISA test for von Willebrand factor using two monoclonal antibodiesJ L Pittet, V Barbalat, M Sanvert, et al.
British Journal of Haematology|December 19, 1998
Identification of new type 2B von Willebrand disease mutations: Arg543Gln, Arg545Pro and Arg578LeuL Hilbert, C Gaucher, J F Abgrall, et al.
Blood|May 1, 1997
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 antibodiesJ Gu, S Jorieux, J M Lavergne, et al.
Thrombosis and Haemostasis|April 1, 1995
Diagnosis of subtype 2B von Willebrand disease in a patient with 2A phenotype of plasma von Willebrand factorC Gaucher, C de Romeuf, M Rauïs-Morret, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|October 1, 1990
Expression in Escherichia coli of a recombinant fragment (Ile 914-Leu 1364) of human von Willebrand factor containing a collagen binding domainS Jorieux, G Piétu, C Gaucher, et al.
Best Practice & Research. Clinical Haematology|November 1, 2001
Type 2 von Willebrand disease causing defective von Willebrand factor-dependent platelet functionD Meyer, E Fressinaud, L Hilbert, et al.
British Journal of Haematology|February 1, 1992
Clinical and biological evaluation in von Willebrand's disease of a von Willebrand factor concentrate with low factor VIII activityJ Goudemand, C Mazurier, A Marey, et al.
Blood|March 15, 1994
Leu 697-->Val mutation in mature von Willebrand factor is responsible for type IIB von Willebrand diseaseL Hilbert, C Gaucher, C de Romeuf, et al.
British Journal of Haematology|October 29, 1998
Type 2N von Willebrand disease due to Arg91Gln substitution and a cytosine deletion in exon 18 of the von Willebrand factor geneA Casonato, C Gaucher, E Pontara, et al.
Pageof 13