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M Aiach

Showing results (41-50 of 236) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|February 28, 1993
Circulating proalbumin associated with a second case of antitrypsin PittsburghS O Brennan, J M Sheat, M Aiach
Thrombosis and Haemostasis|November 1, 2000
The -5061/D polymorphism of the thrombin receptor (PAR-1) gene is not related to myocardial infarction in the ECTIM study. The Etude Cas-Temoins de l'Infarctus du Myocarde. MONICA Members GroupE Arnaud, O Poirier, M Aiach, et al.
Seminars in Thrombosis and Hemostasis|July 1, 1983
Adaptation of synthetic peptide substrate-based assays on a discrete analyzerM Aiach, M Léon, A Michaud, et al.
Revue Neurologique|January 1, 1989
[Thrombopenia with heparin and disseminated intravascular coagulation]J F Vitoux, M Aiach, J N Fiessinger
Seminars in Vascular Medicine|June 17, 2004
Venous thromboembolic disease: risk factors and laboratory investigationM Alhenc-Gelas, M Aiach, P de Moerloose
Thrombosis and Haemostasis|June 1, 1996
First case of sporadic protein S deficiency due to a novel candidate mutation, Ala 484-->Pro, in the protein S active gene (PROS1)D Borgel, B Jude, M Aiach, et al.
Annales De Biologie Clinique|July 27, 2001
[Heparin induced autoimmune thrombocytopenia: assessment of a rapid functional assay]D Lasne, K Tabet, C Bachelot, et al.
Lancet (London, England)|February 15, 1992
Noonan's syndrome and coagulation-factor deficienciesJ Emmerich, M Aiach, L Capron, et al.
Thrombosis and Haemostasis|April 1, 1995
Evaluation of APC resistance in the plasma of patients with Q506 mutation of factor V (factor V Leiden) and treated by oral anticoagulantsY Cadroy, P Sié, M Alhenc-Gelas, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1994
First frameshift mutation in the active protein S gene associated with a quantitative hereditary deficiencyD Borgel, S Gandrille, M Gouault-Heilmann, et al.
Pageof 24

Showing results (41-50 of 236) with videos related to

Sort By:
Pageof 24
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 28, 1993
Circulating proalbumin associated with a second case of antitrypsin PittsburghS O Brennan, J M Sheat, M Aiach
Thrombosis and Haemostasis|November 1, 2000
The -5061/D polymorphism of the thrombin receptor (PAR-1) gene is not related to myocardial infarction in the ECTIM study. The Etude Cas-Temoins de l'Infarctus du Myocarde. MONICA Members GroupE Arnaud, O Poirier, M Aiach, et al.
Seminars in Thrombosis and Hemostasis|July 1, 1983
Adaptation of synthetic peptide substrate-based assays on a discrete analyzerM Aiach, M Léon, A Michaud, et al.
Revue Neurologique|January 1, 1989
[Thrombopenia with heparin and disseminated intravascular coagulation]J F Vitoux, M Aiach, J N Fiessinger
Seminars in Vascular Medicine|June 17, 2004
Venous thromboembolic disease: risk factors and laboratory investigationM Alhenc-Gelas, M Aiach, P de Moerloose
Thrombosis and Haemostasis|June 1, 1996
First case of sporadic protein S deficiency due to a novel candidate mutation, Ala 484-->Pro, in the protein S active gene (PROS1)D Borgel, B Jude, M Aiach, et al.
Annales De Biologie Clinique|July 27, 2001
[Heparin induced autoimmune thrombocytopenia: assessment of a rapid functional assay]D Lasne, K Tabet, C Bachelot, et al.
Lancet (London, England)|February 15, 1992
Noonan's syndrome and coagulation-factor deficienciesJ Emmerich, M Aiach, L Capron, et al.
Thrombosis and Haemostasis|April 1, 1995
Evaluation of APC resistance in the plasma of patients with Q506 mutation of factor V (factor V Leiden) and treated by oral anticoagulantsY Cadroy, P Sié, M Alhenc-Gelas, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1994
First frameshift mutation in the active protein S gene associated with a quantitative hereditary deficiencyD Borgel, S Gandrille, M Gouault-Heilmann, et al.
Pageof 24