Showing results (131-140 of 181) with videos related to

Sort By:
Pageof 19
Annales De Medecine Interne|January 1, 1981
[Diffusion of atherosclerosis in patients with arterial disease of the lower limbs (author's transl)]Y Juillet, J Blanchard, J J Martin, 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.
Thrombosis and Haemostasis|October 1, 1994
Molecular basis of antithrombin type I deficiency: the first large in-frame deletion and two novel mutations in exon 6J Emmerich, G Chadeuf, M Alhenc-Gelas, 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.
Thrombosis and Haemostasis|August 1, 1996
Once-daily subcutaneous dalteparin, a low molecular weight heparin, for the initial treatment of acute deep vein thrombosisJ N Fiessinger, M Lopez-Fernandez, E Gatterer, et al.
Virchows Archiv. A, Pathological Anatomy and Histology|June 23, 1977
Hepatocyte giant mitochondria: an almost constant lesion in systemic sclerodermaG Feldmann, M Maurice, J M Husson, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|February 17, 2000
Protective effect of a thrombin receptor (protease-activated receptor 1) gene polymorphism toward venous thromboembolismE Arnaud, V Nicaud, O Poirier, et al.
Pageof 19