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J Emmerich

Showing results (171-180 of 207) with videos related to

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Blood|August 15, 1997
The A20210 allele of the prothrombin gene is not frequently associated with the factor V Arg 506 to Gln mutation in thrombophilic familiesM Alhenc-Gelas, V Le Cam-Duchez, J Emmerich, et al.
Cardiovascular and Interventional Radiology|June 20, 2019
Endovascular Extra-Anatomic Femoro-Popliteal Bypass for Limb Salvage in Chronic Critical Limb IschemiaM Di Primio, G Angelopoulos, I Lazareth, et al.
Annals of the Rheumatic Diseases|January 15, 2004
Inhibition of leukotriene B4-induced CD11B/CD18 (Mac-1) expression by BIIL 284, a new long acting LTB4 receptor antagonist, in patients with rheumatoid arthritisR Alten, E Gromnica-Ihle, C Pohl, et al.
Journal of Thrombosis and Haemostasis : JTH|March 11, 2004
Incidence and prognosis of cancer associated with bilateral venous thrombosis: a prospective study of 103 patientsA Bura, N Cailleux, B Bienvenu, et al.
British Journal of Anaesthesia|January 20, 2012
Recombinant activated factor VII and prothrombin complex concentrates have different effects on bleeding and arterial thrombosis in the haemodiluted rabbitF Le Saché, B Le Bonniec, P Gaussem, et al.
Journal of Thrombosis and Haemostasis : JTH|June 8, 2012
Lack of association of non-synonymous FUT2 and ALPL polymorphisms with venous thrombosisD-A Tregouet, M Sabater-Lleal, M Bruzelius, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 11, 1999
Complex association of protein C gene promoter polymorphism with circulating protein C levels and thrombotic riskM Aiach, V Nicaud, M Alhenc-Gelas, et al.
Journal of Vascular Surgery|July 1, 1995
Percutaneous transluminal angioplasty for emboligenic arterial lesions after radiotherapy of axillary arteriesC Veyssier-Belot, J Emmerich, M R Sapoval, et al.
Journal of Thrombosis and Haemostasis : JTH|August 12, 2004
The factor II G20210A gene polymorphism, but not factor V Arg506Gln, is associated with peripheral arterial disease: results of a case-control studyJ L Reny, M Alhenc-Gelas, P Fontana, et al.
British Journal of Haematology|July 1, 1991
Molecular basis for hereditary antithrombin III quantitative deficiencies: a stop codon in exon IIIa and a frameshift in exon VIS Gandrille, D Vidaud, J Emmerich, et al.
Pageof 21

Showing results (171-180 of 207) with videos related to

Sort By:
Pageof 21
Blood|August 15, 1997
The A20210 allele of the prothrombin gene is not frequently associated with the factor V Arg 506 to Gln mutation in thrombophilic familiesM Alhenc-Gelas, V Le Cam-Duchez, J Emmerich, et al.
Cardiovascular and Interventional Radiology|June 20, 2019
Endovascular Extra-Anatomic Femoro-Popliteal Bypass for Limb Salvage in Chronic Critical Limb IschemiaM Di Primio, G Angelopoulos, I Lazareth, et al.
Annals of the Rheumatic Diseases|January 15, 2004
Inhibition of leukotriene B4-induced CD11B/CD18 (Mac-1) expression by BIIL 284, a new long acting LTB4 receptor antagonist, in patients with rheumatoid arthritisR Alten, E Gromnica-Ihle, C Pohl, et al.
Journal of Thrombosis and Haemostasis : JTH|March 11, 2004
Incidence and prognosis of cancer associated with bilateral venous thrombosis: a prospective study of 103 patientsA Bura, N Cailleux, B Bienvenu, et al.
British Journal of Anaesthesia|January 20, 2012
Recombinant activated factor VII and prothrombin complex concentrates have different effects on bleeding and arterial thrombosis in the haemodiluted rabbitF Le Saché, B Le Bonniec, P Gaussem, et al.
Journal of Thrombosis and Haemostasis : JTH|June 8, 2012
Lack of association of non-synonymous FUT2 and ALPL polymorphisms with venous thrombosisD-A Tregouet, M Sabater-Lleal, M Bruzelius, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 11, 1999
Complex association of protein C gene promoter polymorphism with circulating protein C levels and thrombotic riskM Aiach, V Nicaud, M Alhenc-Gelas, et al.
Journal of Vascular Surgery|July 1, 1995
Percutaneous transluminal angioplasty for emboligenic arterial lesions after radiotherapy of axillary arteriesC Veyssier-Belot, J Emmerich, M R Sapoval, et al.
Journal of Thrombosis and Haemostasis : JTH|August 12, 2004
The factor II G20210A gene polymorphism, but not factor V Arg506Gln, is associated with peripheral arterial disease: results of a case-control studyJ L Reny, M Alhenc-Gelas, P Fontana, et al.
British Journal of Haematology|July 1, 1991
Molecular basis for hereditary antithrombin III quantitative deficiencies: a stop codon in exon IIIa and a frameshift in exon VIS Gandrille, D Vidaud, J Emmerich, et al.
Pageof 21