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Thrombosis and Haemostasis|June 1, 1997
Purpura fulminans induced by disseminated intravascular coagulation following infection in 2 unrelated children with double heterozygosity for factor V Leiden and protein S deficiencyA Inbal, G Kenet, A Zivelin, et al.
British Journal of Haematology|January 1, 1991
Antithrombin Vicenza, Ala 384 to Pro (GCA to CCA) mutation, transforming the inhibitor into a substrateR Caso, D A Lane, E A Thompson, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|March 11, 2000
Polymorphisms in the 5' regulatory region of the tissue factor gene and the risk of myocardial infarction and venous thromboembolism: the ECTIM and PATHROS studies. Etude Cas-Témoins de l'Infarctus du Myocarde. Paris Thrombosis case-control StudyE Arnaud, V Barbalat, V Nicaud, et al.
British Journal of Haematology|September 21, 2000
Molecular bases of antithrombin deficiency in French families: identification of seven novel mutations in the antithrombin geneV Picard, A Bura, J Emmerich, et al.
Thrombosis and Haemostasis|November 1, 2001
Evidence of a founder effect for the protein C gene 3363 inserted C mutation in thrombophilic pedigrees of French originP Couture, E G Bovill, C Demers, et al.
Thrombosis and Haemostasis|May 6, 1998
Geographic distribution of the 20210 G to A prothrombin variantF R Rosendaal, C J Doggen, A Zivelin, et al.
Thrombosis and Haemostasis|April 1, 1997
Clinical features in 36 patients homozygous for the ARG 506-->GLN factor V mutationJ Emmerich, M Alhenc-Gelas, M F Aillaud, et al.
La Revue De Medecine Interne|July 1, 1989
[Treatment of deep venous thrombosis. Comparative study of a low molecular weight heparin fragment (Fragmin) by the subcutaneous route and standard heparin by the continuous intravenous route. A multicenter study]M Aiach, J N Fiessinger, J F Vitoux, et al.
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