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Annales De Biologie Clinique|January 9, 2004
[Validation of a diagnostic kit for factor V Leiden mutation]S Gandrille, V Remones, M Aiach
Blood|October 1, 1995
Identification of mutations in 90 of 121 consecutive symptomatic French patients with a type I protein C deficiency. The French INSERM Network on Molecular Abnormalities Responsible for Protein C and Protein S deficienciesS Gandrille, M Aiach
Haemostasis|October 1, 1996
Molecular basis for protein C hereditary deficiencyM Aiach, S Gandrille
Thrombosis and Haemostasis|July 1, 1995
A review of mutations causing deficiencies of antithrombin, protein C and protein SM Aiach, S Gandrille, J Emmerich
British Journal of Haematology|May 12, 1998
Lack of sequence variations in the C4b-BP beta-chain in patients with type III protein S deficiency bearing the Ser 460 to Pro mutation: description of two new intragenic isomorphisms in the C4b-BP beta-chain gene (C4BPB)O Morboeuf, M Aiach, S Gandrille
Thrombosis and Haemostasis|July 1, 1997
Protein S deficiencyD Borgel, S Gandrille, M Aiach
Human Mutation|January 1, 1994
Scanning method to establish the molecular basis of protein C deficienciesS Gandrille, M Goossens, M Aiach
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|May 1, 1995
A rapid screening method for the factor V Arg506-->Gln mutationS Gandrille, M Alhenc-Gelas, M Aiach
Biochimica Et Biophysica Acta|January 11, 1994
Arg-129 plays a specific role in the conformation of antithrombin and in the enhancement of factor Xa inhibition by the pentasaccharide sequence of heparinS Najjam, G Chadeuf, S Gandrille, et al.
Thrombosis and Haemostasis|June 1, 1996
First case of sporadic protein S deficiency due to a novel candidate mutation, Ala 484-->Pro, in the protein S active gene (PROS1)D Borgel, B Jude, M Aiach, et al.
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