Prospective evaluation of the ‘4Ts’ score and particle gel immunoassay specific to heparin/PF4 for the diagnosis of heparin‐induced thrombocytopenia von POUPLARD, C., GUERET, P., FOUASSIER, M., TERNISIEN, C., TROSSAERT, M., RÉGINA, S., GRUEL, Y.

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Cross‐reactivity of human anti‐FVIII antibodies to porcine rFVIII: French field study to validate the modified Nijmegen method von Le Cam Duchez, V., Ternisien, C., Guery, E. A., Eschwège, V., Jeanpierre, E., Nougier, C., Proulle, V., Stepanian, A., Tuffigo, M., Marlu, R., Pouplard, C.

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Diagnosis and management challenges in patients with mild haemophilia A and discrepant FVIII measurements von Trossaert, M., Lienhart, A., Nougier, C., Fretigny, M., Sigaud, M., Meunier, S., Fouassier, M., Ternisien, C., Negrier, C., Dargaud, Y.

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Platelet function analyser (PFA-100) results and von Willebrand factor deficiency: a 16-year 'real-world' experience von Ardillon, L., Ternisien, C., Fouassier, M., Sigaud, M., Lefrançois, A., Pacault, M., Ribeyrol, O., Fressinaud, E., Boisseau, P., Trossaërt, M.

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Confirmed validation of an innovative PCR-assay without DNA extraction for multiplex diagnosis of factor V Leiden and prothrombin gene variants von Desjonquères, A., Ménard, A., Detemmerman, L., Ternisien, C., Fouassier, M., Gillet, B., Béné, M.C., Le Bris, Y.

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Prevalence, biological phenotype and genotype in moderate/mild hemophilia A with discrepancy between one‐stage and chromogenic factor VIII activity von TROSSAËRT, M., BOISSEAU, P., QUEMENER, A., SIGAUD, M., FOUASSIER, M., TERNISIEN, C., LEFRANÇOIS‐BETTEMBOURG, A., TESSON, C., THOMAS, C., BEZIEAU, S.

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Discrepancies between one stage assay and chromogenic substrate assay in patients treated with recombinant or plasma-derived FVIII and usefulness of a specific standard in ReFacto... von Pouplard, C., Ternisien, C., Desconclois, C., Lasne, D., Aillaud, M.-F., Caron, C.

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Hémophilie A acquise. Étude d’une série rétrospective monocentrique de 39 patients von Graveleau, J., Trossaërt, M., Leux, C., Masseau, A., Ternisien, C., Néel, A., Fouassier, M., Agard, C., Sigaud, M., Hamidou, M.

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Agreement between factor XIII activity and antigen assays in measurement of factor XIII: A French multicenter study of 147 human plasma samples von Caron, C., Meley, R., Le Cam Duchez, V., Aillaud, M. F., Lavenu‐Bombled, C., Dutrillaux, F., Flaujac, C., Ryman, A., Ternisien, C., Lasne, D., Galinat, H., Pouplard, C.

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Validation of the first commercial ELISA for type 2N von Willebrand's disease diagnosis von VEYRADIER, A., CARON, C., TERNISIEN, C., WOLF, M., TROSSAERT, M., FRESSINAUD, E., GOUDEMAND, J.

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The use of the new ReFacto AF Laboratory Standard allows reliable measurement of FVIII:C levels in ReFacto AF mock plasma samples by a one-stage clotting assay von POUPLARD, C., CARON, C., AILLAUD, M. F., TERNISIEN, C., DESCONCLOIS, C., DUBANCHET, A., SOBAS, F.

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Does the presence of von Willebrand factor in FVIII-deficient plasma influences the measurement of FVIII inhibitor titres in haemophilia A patients? von Pouplard, C., Desconclois, C., Sobas, F., Aillaud, M. F., Ternisien, C., Caron, C.

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An unexpected transmission of von Willebrand disease type 3: the first case of maternal uniparental disomy 12 von BOISSEAU, Pierre, GIRAUD, Mathilde, TERNISIEN, Catherine, VEYRADIER, Agnès, FRESSINAUD, Edith, LEFRANCOIS, Armelle, BEZIEAU, Stéphane, FOUASSIER, Marc

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Management of bleeding in severe factor V deficiency with a factor V inhibitor von Ardillon, L., Lefrançois, A., Graveleau, J., Fouassier, M., Ternisien, C., Sigaud, M., Fretigny, M., Archambeaud, I., Trossaërt, M.

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Fibrinogen angers with a new deletion (γ GVYYQ 346‐350) causes hypofibrinogenemia with hepatic storage von DIB, N., QUELIN, F., TERNISIEN, C., HANSS, M., MICHALAK, S., DE MAZANCOURT, P., ROUSSELET, M. C., CALÈS, P.

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Acquired hemophilia A. A monocentric retrospective study of 39 patients von Graveleau, J, Trossaërt, M, Leux, C, Masseau, A, Ternisien, C, Néel, A, Fouassier, M, Agard, C, Sigaud, M, Hamidou, M

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A novel panel of blood markers to assess the degree of liver fibrosis von Calès, Paul, Oberti, Frédéric, Michalak, Sophie, Hubert-Fouchard, Isabelle, Rousselet, Marie-Christine, Konaté, Anselme, Gallois, Yves, Ternisien, Catherine, Chevailler, Alain, Lunel, Françoise

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Intérêt d’explorations complémentaires devant des taux d’antithrombine limites pour authentifier un déficit responsable d’un risque thrombotique von Tessier, Dolores, Ternisien, C., Espitia, O., Durant, C., Ahlenc-Gelas, M., Connault, J.

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Thrombotic risk according to SERPINC1 genotype in a large cohort of subjects with antithrombin inherited deficiency von Alhenc-Gelas, Martine, Plu-Bureau, Genevieve, Hugon-Rodin, Justine, Picard, Veronique, Horellou, Marie-Helene

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PB0818 Impact of ABO Blood Group Genotype on VWF Level in Carriers of Type 3 von Willebrand Disease from the French von Willebrand Disease Reference Center von Kitel, C., Jeanpierre, E., Boisseau, P., Ternisien, C., Desvages, M., Rauch, A., Paris, C., Daniel, M., Geffroy, S., Duployez, N., Goudemand, J., Morange, P., Zawadzki, C., Susen, S.

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