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S Gandrille

Showing results (41-50 of 64) with videos related to

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Thrombosis and Haemostasis|June 1, 1994
Influence of six mutations of the protein C gene on the Gla domain conformation and calcium affinityP Gaussem, S Gandrille, J Duchemin, et al.
Blood|July 1, 1993
Five novel mutations located in exons III and IX of the protein C gene in patients presenting with defective protein C anticoagulant activityS Gandrille, M Alhenc-Gelas, P Gaussem, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 9, 1999
Mutations in promoter region of thrombomodulin and venous thromboembolic diseaseL Le Flem, V Picard, J Emmerich, et al.
Thrombosis and Haemostasis|January 11, 1993
Protein C deficiency: a database of mutations. For the Protein C & S Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and HaemostasisP H Reitsma, S R Poort, F Bernardi, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 1, 1995
Protein C infusion in a patient with inherited protein C deficiency caused by two missense mutations: Arg 178 to Gln and Arg-1 to HisM Alhenc-Gelas, J Emmerich, S Gandrille, et al.
Thrombosis and Haemostasis|June 16, 1988
A study of fibrinogen and fibrinolysis in 10 adults with nephrotic syndromeS Gandrille, M H Jouvin, P Toulon, et al.
British Journal of Haematology|July 1, 1991
Molecular basis for hereditary antithrombin III quantitative deficiencies: a stop codon in exon IIIa and a frameshift in exon VIS Gandrille, D Vidaud, J Emmerich, et al.
Thrombosis and Haemostasis|March 11, 1998
Protein S deficiency: different biological phenotypes according to the assays usedD Brunet, M C Barthet, P E Morange, et al.
British Journal of Haematology|October 16, 1999
Influence of three potential genetic risk factors for thrombosis in 43 families carrying the factor V Arg 506 to Gln mutationV Le Cam-Duchez, S Gandrille, D Trégouët, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 11, 1999
Complex association of protein C gene promoter polymorphism with circulating protein C levels and thrombotic riskM Aiach, V Nicaud, M Alhenc-Gelas, et al.
Pageof 7

Showing results (41-50 of 64) with videos related to

Sort By:
Pageof 7
Thrombosis and Haemostasis|June 1, 1994
Influence of six mutations of the protein C gene on the Gla domain conformation and calcium affinityP Gaussem, S Gandrille, J Duchemin, et al.
Blood|July 1, 1993
Five novel mutations located in exons III and IX of the protein C gene in patients presenting with defective protein C anticoagulant activityS Gandrille, M Alhenc-Gelas, P Gaussem, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 9, 1999
Mutations in promoter region of thrombomodulin and venous thromboembolic diseaseL Le Flem, V Picard, J Emmerich, et al.
Thrombosis and Haemostasis|January 11, 1993
Protein C deficiency: a database of mutations. For the Protein C & S Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and HaemostasisP H Reitsma, S R Poort, F Bernardi, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 1, 1995
Protein C infusion in a patient with inherited protein C deficiency caused by two missense mutations: Arg 178 to Gln and Arg-1 to HisM Alhenc-Gelas, J Emmerich, S Gandrille, et al.
Thrombosis and Haemostasis|June 16, 1988
A study of fibrinogen and fibrinolysis in 10 adults with nephrotic syndromeS Gandrille, M H Jouvin, P Toulon, et al.
British Journal of Haematology|July 1, 1991
Molecular basis for hereditary antithrombin III quantitative deficiencies: a stop codon in exon IIIa and a frameshift in exon VIS Gandrille, D Vidaud, J Emmerich, et al.
Thrombosis and Haemostasis|March 11, 1998
Protein S deficiency: different biological phenotypes according to the assays usedD Brunet, M C Barthet, P E Morange, et al.
British Journal of Haematology|October 16, 1999
Influence of three potential genetic risk factors for thrombosis in 43 families carrying the factor V Arg 506 to Gln mutationV Le Cam-Duchez, S Gandrille, D Trégouët, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 11, 1999
Complex association of protein C gene promoter polymorphism with circulating protein C levels and thrombotic riskM Aiach, V Nicaud, M Alhenc-Gelas, et al.
Pageof 7