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P Toulon

Showing results (31-40 of 39) with videos related to

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European Journal of Clinical Investigation|June 1, 1991
Involvement of heparin cofactor II in chymotrypsin neutralization and in the pancreatic proteinase-antiproteinase interaction during acute pancreatitis in manP Toulon, G Chadeuf, J L Bouillot, et al.
Thrombosis and Haemostasis|July 1, 1996
The relationship between plasma microparticles, protein S and anticardiolipin antibodies in patients with human immunodeficiency virus infectionJ C Gris, P Toulon, S Brun, et al.
Intensive Care Medicine|January 1, 1992
Effects of aprotinin on hemorrhagic complications in ARDS patients during prolonged extracorporeal CO2 removalF Brunet, J P Mira, M Belghith, 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.
Thrombosis and Haemostasis|December 18, 1987
Circulating activities during constant infusion of heparin or a low molecular weight derivative (enoxaparine): failure to demonstrate any circadian variationsP Toulon, J F Vitoux, C Leroy, et al.
Thrombosis and Haemostasis|June 16, 1988
A study of fibrinogen and fibrinolysis in 10 adults with nephrotic syndromeS Gandrille, M H Jouvin, P Toulon, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 11, 2000
Screening for abnormalities of the protein C anticoagulant pathway using the ProC Global assay. Results of a European multicenter evaluationP Toulon, W M Halbmeyer, G Hafner, et al.
Human Mutation|January 1, 1992
Two novel mutations responsible for hereditary type I protein C deficiency: characterization by denaturing gradient gel electrophoresisS Gandrille, M Vidaud, M Aiach, 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.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
European Journal of Clinical Investigation|June 1, 1991
Involvement of heparin cofactor II in chymotrypsin neutralization and in the pancreatic proteinase-antiproteinase interaction during acute pancreatitis in manP Toulon, G Chadeuf, J L Bouillot, et al.
Thrombosis and Haemostasis|July 1, 1996
The relationship between plasma microparticles, protein S and anticardiolipin antibodies in patients with human immunodeficiency virus infectionJ C Gris, P Toulon, S Brun, et al.
Intensive Care Medicine|January 1, 1992
Effects of aprotinin on hemorrhagic complications in ARDS patients during prolonged extracorporeal CO2 removalF Brunet, J P Mira, M Belghith, 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.
Thrombosis and Haemostasis|December 18, 1987
Circulating activities during constant infusion of heparin or a low molecular weight derivative (enoxaparine): failure to demonstrate any circadian variationsP Toulon, J F Vitoux, C Leroy, et al.
Thrombosis and Haemostasis|June 16, 1988
A study of fibrinogen and fibrinolysis in 10 adults with nephrotic syndromeS Gandrille, M H Jouvin, P Toulon, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 11, 2000
Screening for abnormalities of the protein C anticoagulant pathway using the ProC Global assay. Results of a European multicenter evaluationP Toulon, W M Halbmeyer, G Hafner, et al.
Human Mutation|January 1, 1992
Two novel mutations responsible for hereditary type I protein C deficiency: characterization by denaturing gradient gel electrophoresisS Gandrille, M Vidaud, M Aiach, 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.
Pageof 4