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S Gandrille

Showing results (21-30 of 64) with videos related to

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Proteins|March 29, 2001
Three-dimensional model of the SHBG-like region of anticoagulant protein S: new structure-function insightsB O Villoutreix, B Dahlbäck, D Borgel, et al.
Thrombosis Research|October 29, 2000
Expression and characterization of recombinant protein S with the Ser 460 Pro mutationO Morboeuf, D Borgel, M Aiach, et al.
Presse Medicale (Paris, France : 1983)|September 24, 1994
[A new cause of familial thrombophilia: resistance to the effect of activated protein C]J Emmerich, M Alhenc-Gelas, S Gandrille, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1992
Molecular abnormalities responsible for thrombosis. Genetic aspectsM Aiach, S Gandrille, J Emmerich, et al.
British Journal of Haematology|March 1, 1988
Association of inherited dysfibrinogenaemia and protein C deficiency in two unrelated familiesS Gandrille, P Priollet, L Capron, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 5, 1998
Homozygous protein C deficiency with a double variant His 202 to Tyr and Ala 346 to ThrS Kemahli, M Alhenc-Gelas, S Gandrille, et al.
Seminars in Hematology|July 1, 1997
Protein C and protein S deficienciesM Aiach, D Borgel, P Gaussem, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1991
Genetic diagnosis of qualitative and quantitative antithrombin III deficienciesE Clauser, S Gandrille, D Vidaud, et al.
The Journal of Laboratory and Clinical Medicine|August 1, 1996
Molecular basis for protein S hereditary deficiency: genetic defects observed in 118 patients with type I and type IIa deficiencies. The French Network on Molecular Abnormalities Responsible for Protein C and Protein S DeficienciesD Borgel, J Duchemin, M Alhenc-Gelas, et al.
Nephron|January 1, 1992
Significance of high levels of heparin cofactor II in the plasma and urine of adult patients with nephrotic syndromeP Toulon, S Gandrille, P Remy, et al.
Pageof 7

Showing results (21-30 of 64) with videos related to

Sort By:
Pageof 7
Proteins|March 29, 2001
Three-dimensional model of the SHBG-like region of anticoagulant protein S: new structure-function insightsB O Villoutreix, B Dahlbäck, D Borgel, et al.
Thrombosis Research|October 29, 2000
Expression and characterization of recombinant protein S with the Ser 460 Pro mutationO Morboeuf, D Borgel, M Aiach, et al.
Presse Medicale (Paris, France : 1983)|September 24, 1994
[A new cause of familial thrombophilia: resistance to the effect of activated protein C]J Emmerich, M Alhenc-Gelas, S Gandrille, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1992
Molecular abnormalities responsible for thrombosis. Genetic aspectsM Aiach, S Gandrille, J Emmerich, et al.
British Journal of Haematology|March 1, 1988
Association of inherited dysfibrinogenaemia and protein C deficiency in two unrelated familiesS Gandrille, P Priollet, L Capron, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 5, 1998
Homozygous protein C deficiency with a double variant His 202 to Tyr and Ala 346 to ThrS Kemahli, M Alhenc-Gelas, S Gandrille, et al.
Seminars in Hematology|July 1, 1997
Protein C and protein S deficienciesM Aiach, D Borgel, P Gaussem, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1991
Genetic diagnosis of qualitative and quantitative antithrombin III deficienciesE Clauser, S Gandrille, D Vidaud, et al.
The Journal of Laboratory and Clinical Medicine|August 1, 1996
Molecular basis for protein S hereditary deficiency: genetic defects observed in 118 patients with type I and type IIa deficiencies. The French Network on Molecular Abnormalities Responsible for Protein C and Protein S DeficienciesD Borgel, J Duchemin, M Alhenc-Gelas, et al.
Nephron|January 1, 1992
Significance of high levels of heparin cofactor II in the plasma and urine of adult patients with nephrotic syndromeP Toulon, S Gandrille, P Remy, et al.
Pageof 7