Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation by Casini, A., Brungs, T., Lavenu‐Bombled, C., Vilar, R., Neerman‐Arbez, M., Moerloose, P.

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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 by 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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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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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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Common variable immunodeficiency patient classification based on impaired B cell memory differentiation correlates with clinical aspects by PIQUERAS, B, LAVENU-BOMBLED, C, GALICIER, L, BERGERON-VAN DER CRUYSSEN, F, MOUTHON, L, CHEVRET, S, DEBRE, P, SCHMITT, C, OKSENHENDLER, E

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Probing platelet factor 4 α‐granule targeting by Briquet‐Laugier, V., Lavenu‐Bombled, C., Schmitt, A., Leboeuf, M., Uzan, G., Dubart‐Kupperschmitt, A., Rosa, J.‐P.

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High prevalence of the natural Asn89Asp mutation in the GP1BB gene associated with Bernard–Soulier syndrome in French patients from the genetic isolate of Reunion Island by Fiore, Mathieu, De Thoré, Céline, Randrianaivo‐Ranjatoelina, Hanitra, Baas, Marie‐Jeanne, Jacquemont, Marie‐Line, Dreyfus, Marie, Lavenu‐Bombled, Cécile, Li, Renhao, Gachet, Christian, Dupuis, Arnaud, Lanza, Francois

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Interleukin-13 gene expression is regulated by GATA-3 in T cells: role of a critical association of a GATA and two GATG motifs by Lavenu-Bombled, Cecile, Trainor, Cecelia D, Makeh, Iman, Romeo, Paul-Henri, Max-Audit, Isabelle

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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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Thrombopoietin-induced Dami cells as a model for α-granule biogenesis by Briquet-Laugier, Véronique, El.Golli, Nargès, Nurden, Paquita, Lavenu-Bombled, Cécile, Dubart-Kupperschmitt, Anne, Nurden, Alan, Rosa, Jean-Philippe

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