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J Emmerich

Showing results (151-160 of 207) with videos related to

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Journal De Medecine Vasculaire|November 7, 2022
Peri-procedural complications following endovascular revascularization for critical limb ischemiaA Compagnon, I Lazareth, A Fels, 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.
Thrombosis and Haemostasis|March 1, 1995
Portal vein thrombosis and factor V Arg 506 to Gln mutationD Levoir, J Emmerich, M Alhenc-Gelas, 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.
Lancet (London, England)|February 4, 1995
Myocardial infarction, Arg 506 to Gln factor V mutation, and activated protein C resistanceJ Emmerich, O Poirier, A Evans, 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.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|December 1, 1994
Three novel mutations of antithrombin inducing high-molecular-mass compoundsJ Emmerich, D Vidaud, M Alhenc-Gelas, 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.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|October 1, 1996
Homozygous variant of antithrombin with lack of affinity for heparin: management of severe thrombotic complications associated with intrauterine fetal demiseA Bauters, C Zawadzki, A Bura, et al.
The Journal of Biological Chemistry|March 6, 1992
Human lipoprotein lipase. Analysis of the catalytic triad by site-directed mutagenesis of Ser-132, Asp-156, and His-241J Emmerich, O U Beg, J Peterson, et al.
Pageof 21

Showing results (151-160 of 207) with videos related to

Sort By:
Pageof 21
Journal De Medecine Vasculaire|November 7, 2022
Peri-procedural complications following endovascular revascularization for critical limb ischemiaA Compagnon, I Lazareth, A Fels, 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.
Thrombosis and Haemostasis|March 1, 1995
Portal vein thrombosis and factor V Arg 506 to Gln mutationD Levoir, J Emmerich, M Alhenc-Gelas, 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.
Lancet (London, England)|February 4, 1995
Myocardial infarction, Arg 506 to Gln factor V mutation, and activated protein C resistanceJ Emmerich, O Poirier, A Evans, 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.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|December 1, 1994
Three novel mutations of antithrombin inducing high-molecular-mass compoundsJ Emmerich, D Vidaud, M Alhenc-Gelas, 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.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|October 1, 1996
Homozygous variant of antithrombin with lack of affinity for heparin: management of severe thrombotic complications associated with intrauterine fetal demiseA Bauters, C Zawadzki, A Bura, et al.
The Journal of Biological Chemistry|March 6, 1992
Human lipoprotein lipase. Analysis of the catalytic triad by site-directed mutagenesis of Ser-132, Asp-156, and His-241J Emmerich, O U Beg, J Peterson, et al.
Pageof 21