Marianne Sigaud

Mild hemophilia A with factor VIII assay discrepancy: using thrombin generation assay to assess the bleeding phenotype

Marc Trossaërt, Véronique Regnault, Marianne Sigaud et al. · Journal of Thrombosis and Haemostasis · 2008 · 84 citations · Full text

Thrombin Generation, Thrombosis, Laboratory Hematology +10

Therapeutic monitoring of von Willebrand disease: interest and limits of a platelet function analyser at high shear rates

Édith Fressinaud, Agnès Veyradier, Marianne Sigaud et al. · British Journal of Haematology · 1999 · 75 citations · Full text

Type 2M, Platelet Vwf, Pharmacotherapy +19

Molecular basis of severe factor XI deficiency in seven families from the west of France. Seven novel mutations, including an ancient Q88X mutation

Florence Quélin, Marc Trossaërt, Marianne Sigaud et al. · Journal of Thrombosis and Haemostasis · 2004 · 61 citations

Mendelian Disorder, Genetic Disorder, Genetics +8

Prevalence, biological phenotype and genotype in moderate/mild hemophilia A with discrepancy between one‐stage and chromogenic factor VIII activity

Marc Trossaërt, Pierre Boisseau, Agnès Quéméner et al. · Journal of Thrombosis and Haemostasis · 2010 · 55 citations · Full text

Diagnosis and management challenges in patients with mild haemophilia A and discrepant <scp>FVIII</scp> measurements

Marc Trossaërt, Anne Lienhart, Christophe Nougier et al. · Haemophilia · 2014 · 51 citations