Search Results - "Itzhar, N."

OC 60.5 Response to Desmopressin in Type 2N Von Willebrand’s Disease: A Genotype-Phenotype Analysis on a Cohort of 121 Patients by Daniel, M., Rauch, A., Volot, F., Pouymayou, K., Pan-Petesch, B., Castet, S., Itzhar, N., Veyradier, A., Repessé, Y., Ternisien, C., Trossaert, M., Boisseau, P., Jeanpierre, E., Paris, C., Zawadzki, C., Desvages, M., Dupont, A., Goudemand, J., Susen, S.

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P3277Distinct differences in laboratory findings of patients with von Willebrand disease type 2A versus patients with LVAD-induced acquired von Willebrand syndrome by Deconinck, S., Tersteeg, C., Bailleul, E., Delrue, L., Vandeputte, N., Pareyn, I., Deckmyn, H., De Meyer, S.F., Itzhar-Baikian, N., Vanhoorelbeke, K., Vanderheyden, M.

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Combined factor V and VIII deficiency and pregnancy – Need for an early protocol-based multidisciplinary management by Hoffmann, C., Falzone, E., Mihai, A., Gitz, L., Itzhar-Baikian, N., Martel-Jacob, S., Mercier, F.J.

“…We report the medical management of a 32-year-old primigravida, after she was found to have a combined factor V (FV) and factor VIII (FVIII) deficiency during…”
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