Novel mutations associated with a discrepancy between one-stage and chromogenic FVIII activity assays von Provaznikova, D., Houskova, K., Radovska, A., Salaj, P., Hrachovinova, I.

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CCAAT/enhancer-binding protein alpha (CEBPA) polymorphisms and mutations in healthy individuals and in patients with peripheral artery disease, ischaemic heart disease and hyperlip... von Fuchs, O, Kostecka, A, Provazníková, D, Krásná, B, Kotlín, R, Stanková, M, Kobylka, P, Dostálová, G, Zeman, M, Chochola, M

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PB0849 Importance of VWF:CB Assay in Diagnosis of 2M VWD von Provaznikova, D., Marecek, F., Geierova, V., Radovska, A., Simonikova, M., Liskova, R., Pohlreichova, V., Hrachovinova, I.

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PB0237 Inhibitor in Congenital FXI Deficiency von Fenclová, T., Provaznikova, D., Liskova, R., Radovska, A., Simonikova, M., Louzil, J., Cespivová, D., Marecek, F., Salaj, P., Hrachovinova, I.

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CCAAT/Enhancer-Binding Protein [alpha] (CEBPA) Polymorphisms and Mutations in Healthy Individuals and in Patients with Peripheral Artery Disease, Ischaemic Heart Disease and Hyperl... von Fuchs, O, Kostecka, A, Provazníková, D, Krásná, B, Kotlín, R, Stanková, M, Kobylka, P, Dostálová, G, Zeman, M, Chochola, M

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PB0855 New Mutation in CK Domain of VWF Gene in Patient with Type 2N von Willebrand Disease von Zolkova, J., Kolkova, Z., Loderer, D., Provaznikova, D., Hrachovinova, I., Sokol, J., Simurda, T., Lisá, L., Dobrotová, M., Ivanková, J., Skornova, I., Lasabova, Z., Stasko, J.

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Promyelocytic leukaemia protein and defect in transforming growth factor-beta signal pathway in acute promyelocytic leukaemia von Fuchs, O, Provazníková, D, Peslová, G

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P001 Acute myeloid leukemia, myelodysplastic syndrome, multiple myeloma and non-Hodgkin's lymphoma carrying mutated CCAAT/enhancer-binding protein alpha von Fuchs, O, Provaznikova, D, Kocova, M, Kostecka, A, Neuwirtova, R, Kobylka, P, Cermak, J, Brezinova, J, Schwarz, J, Salaj, P, Benesova, K

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Intracranial pressure monitoring in patients with acute brain injury in the intensive care unit (SYNAPSE-ICU): an international, prospective observational cohort study von Robba, Chiara, Rebora, Paola, Taccone, Fabio S, Prisco, Lara, Vincent, Jean-Louis, Citerio, Giuseppe, Abed Maillard, S., Anglada, M., Badenes, R., Bajracharya, T., Banco, P., Batista, D., Besch, G., Brunetti, I., Caillard, A., Calamai, I., Caricato, A., Casanova, M., Cavaleiro, P., Celaya Lopez, M., Chauhan, R., Cinotti, R., Cortegiani, A., Cotoia, A., Davidovich, V., Del Bianco, S., Diakaki, C., Dibu, J., Dimoula, A., Dominguez, L.J.Y., Duque, P., Efthymiou, A., Favre Eva, E., Fencl, M., Forjan, P., Freitas, R., Fumale, M., Gelormini, C., Giugni, A., Glorieux, D., Gonzalez Perez, M.I., Griesdale, D., Gritsan, A., Grotheer, S., Hawthorne, C., Iasonidou, C., Ioannoni, E., Kafle, P., Kandamby, D.H., Khomiakov, S., Kilapong, B., Kojder, K., Kontoudaki, E., Koukoulitsios, G., Kovac, N., Kozar, S., Kurtz, P., Lamperti, M., Lavicka, P., Lencastre, L., López Ojeda, P., Lores, A., Magni, F., Majholm, B., Maskey, S., Miroz, J.P., Montes, J.M., Motta, A., Mouloudi, E., Olson, D., Pacheco, C., Palli, E., Panda, N., Pantelas, N., Pinedo Portilla, J.L., Reade, M., Rigamonti, A., Rivera, L.L., Roka, Y.B., Sapra, H., Serrano, A., Shrestha, G.S., Shum, H.P., Silva, S., Simoes, M., Sivakumar, S., Skola, J., Škoti, M., Spatenkova, V., Stamou, E.E., Olson, Z., Tánczos, K., Thompson, C., Tsikriki, S., Van De Velde, S., Vrettou, C., Westy Hoffmeyer, H., Wolf, S., Yasin Wayhs, S., Zerbi, S.M.

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S65C and other mutations in the haemochromatosis gene in the Czech population von Cimburova, M, Putova, I, Provaznikova, H, Pinterova, D, Horak, J

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