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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.
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.
Seminars in Hematology|July 1, 1997
Protein C and protein S deficienciesM Aiach, D Borgel, P Gaussem, et al.
The Journal of Laboratory and Clinical Medicine|April 1, 1995
Mechanism of protein C deficiency in a patient with arginine 358 alpha 1-antitrypsin (Pittsburgh mutation): role in the maintenance of hemostatic balanceJ Emmerich, M Alhenc-Gelas, S Gandrille, et al.
Thrombosis and Haemostasis|February 19, 1990
A plasma clot lysis assay based on the release of fibrin degradation products: application to the diagnosis of hypofibrinolytic statesP Gaussem, S Gandrille, P Molho-Sabatier, et al.
Thrombosis and Haemostasis|March 1, 1996
Five novel mutations of the protein S active gene (PROS 1) in 8 Norman familiesJ Duchemin, J Y Borg, D Borgel, et al.
Thrombosis and Haemostasis|November 1, 2000
Characterization of cleaved plasma protein S with a monoclonal antibody-based assayO Morboeuf, D Borgel, P Gaussem, et al.
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.
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