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Showing results (251-260 of 315) with videos related to

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La Revue De Medecine Interne|December 19, 2006
[Endovascular repair of a tuberculous aortic false aneurysm]O Steichen, O Pellerin, M Frank, et al.
Presse Medicale (Paris, France : 1983)|October 10, 1998
[Leriche syndrome in a case of atrophic polychondritis]J G Velut, E Héron, P Cohen, et al.
Thrombosis and Haemostasis|June 1, 1994
Adjusted versus fixed doses of the low-molecular-weight heparin fragmin in the treatment of deep vein thrombosis. Fragmin-Study GroupM Alhenc-Gelas, C Jestin-Le Guernic, J F Vitoux, et al.
Dermatologica|January 1, 1986
Von Recklinghausen neurofibromatosis and hereditary plasminogen deficiencyP Priollet, M Roncato, M Vayssairat, et al.
The Journal of Clinical Investigation|October 1, 1989
Molecular characterization of antithrombin III (ATIII) variants using polymerase chain reaction. Identification of the ATIII Charleville as an Ala 384 Pro mutationP Molho-Sabatier, M Aiach, I Gaillard, et al.
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.
Journal Des Maladies Vasculaires|January 1, 1981
[Evaluation of the spread of atherosclerosis in patients with arteritis. Implications for the therapeutic indications (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.
The American Journal of Medicine|May 1, 1992
Antiphospholipid antibodies and atherosclerosisV Lecerf, M Alhenc-Gelas, C Laurian, 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.
Pageof 32

Showing results (251-260 of 315) with videos related to

Sort By:
Pageof 32
La Revue De Medecine Interne|December 19, 2006
[Endovascular repair of a tuberculous aortic false aneurysm]O Steichen, O Pellerin, M Frank, et al.
Presse Medicale (Paris, France : 1983)|October 10, 1998
[Leriche syndrome in a case of atrophic polychondritis]J G Velut, E Héron, P Cohen, et al.
Thrombosis and Haemostasis|June 1, 1994
Adjusted versus fixed doses of the low-molecular-weight heparin fragmin in the treatment of deep vein thrombosis. Fragmin-Study GroupM Alhenc-Gelas, C Jestin-Le Guernic, J F Vitoux, et al.
Dermatologica|January 1, 1986
Von Recklinghausen neurofibromatosis and hereditary plasminogen deficiencyP Priollet, M Roncato, M Vayssairat, et al.
The Journal of Clinical Investigation|October 1, 1989
Molecular characterization of antithrombin III (ATIII) variants using polymerase chain reaction. Identification of the ATIII Charleville as an Ala 384 Pro mutationP Molho-Sabatier, M Aiach, I Gaillard, et al.
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.
Journal Des Maladies Vasculaires|January 1, 1981
[Evaluation of the spread of atherosclerosis in patients with arteritis. Implications for the therapeutic indications (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.
The American Journal of Medicine|May 1, 1992
Antiphospholipid antibodies and atherosclerosisV Lecerf, M Alhenc-Gelas, C Laurian, 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.
Pageof 32