Moderate factor XI deficiency and neuraxial procedures in an obstetric cohort: a retrospective study (2014–2021) by Billeret, M., Blandinières, A., Touati, D., Desconclois, C., Garreau, R., Le Gouez, A., Lavenu-Bombled, C., Bruyère, M.

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Thrombocytopenia in pregnant patients with mild COVID-19 by Le Gouez, A., Vivanti, A.J., Benhamou, D., Desconclois, C., Mercier, F.J.

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Multiplate whole blood impedance aggregometry: a new tool for von Willebrand disease by VALARCHE, V., DESCONCLOIS, C., BOUTEKEDJIRET, T., DREYFUS, M., PROULLE, V.

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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... by Pouplard, C., Ternisien, C., Desconclois, C., Lasne, D., Aillaud, M.-F., Caron, C.

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Perioperative management and neuraxial analgesia in women with factor XI deficiency (<60 IU/dL): a French multicenter observational study of 314 pregnancies by Flaujac, C., Faille, D., Lavenu-Bombled, C., Drillaud, N., Lasne, D., Billoir, P., Desconclois, C., Touzet, L., Lebreton, A., Diaz-Cau, I., d’Oiron, R., Giansily-Blaizot, M., Wibaut, B., Beurrier, P., Volot, F., Rugeri, L., Roussel-Robert, V., de Raucourt, E.

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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 by 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? by Pouplard, C., Desconclois, C., Sobas, F., Aillaud, M. F., Ternisien, C., Caron, C.

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Mild hemophilia A fortuitously discovered during Henoch-Schönlein purpura by Joly, B, d'Oiron, R, Desconclois, C, Bendelac, L, Rafowicz, A, Meyzer, C, Labrune, P, Veyradier, A

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Découverte fortuite d’une hémophilie A mineure à l’occasion d’un purpura rhumatoïde by Joly, B., d’Oiron, R., Desconclois, C., Bendelac, L., Rafowicz, A., Meyzer, C., Labrune, P., Veyradier, A.

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OC 75.2 Obstetrical Complications in Hereditary Fibrinogen Disorders: The Fibrinogest Study by Hugon-Rodin, J., Carrière, C., Trillot, N., Drillaud, N., Biron, C., Barbay, V., Chamouni, P., Lavenu Bombled, C., Lebreton, A., Wieland, A., Moussa, M., Brungs, T., Tardy, B., Desconclois, C., Beurrier, P., Gay, V., Clasyssens, S., De Maistre, E., Simurda, T., Casini, A.

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

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