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The Journal of Clinical Investigation|May 1, 1992
Met 358 to Arg mutation of alpha 1-antitrypsin associated with protein C deficiency in a patient with mild bleeding tendencyD Vidaud, J Emmerich, M Alhenc-Gelas, 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.Presse Medicale (Paris, France : 1983)|July 12, 1997
[Evaluation of a test for rapid detection of D-dimers for the exclusion of the diagnosis of venous thrombosis]F Jacq, E Héron, A Rance, et al.Journal De Radiologie|August 1, 2000
[Pulmonary embolism: is scintigraphy useful after initial angio-CT?]J F Paul, J N Fiessinger, A Hernigou, et al.Thrombosis Research|November 1, 1994
A phenylalanine 402 to leucine mutation is responsible for a stable inactive conformation of antithrombinJ Emmerich, G Chadeuf, M J Coetzee, et al.La Revue De Medecine Interne|December 19, 2006
[Endovascular repair of a tuberculous aortic false aneurysm]O Steichen, O Pellerin, M Frank, et al.Journal of Computer Assisted Tomography|November 17, 2001
Follow-up electron beam CT for the management of early phase Takayasu arteritisJ F Paul, J N Fiessinger, M Sapoval, et al.Thrombosis and Haemostasis|May 11, 1999
Venous thromboembolic disease and the prothrombin, methylene tetrahydrofolate reductase and factor V genesM Alhenc-Gelas, E Arnaud, V Nicaud, 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.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.Pageof 28