Founder effect is responsible for the p.Leu131Phe heparin‐binding‐site antithrombin mutation common in Hungary: phenotype analysis in a large cohort by Gindele, R., Oláh, Z., Ilonczai, P., Speker, M., Udvari, Á., Selmeczi, A., Pfliegler, G., Marján, E., Kovács, B., Boda, Z., Muszbek, L., Bereczky, Z.

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C0290: Diagnostic Considerations Based on the Experience of Genetic Analysis in Protein S Deficiency in the Hungarian Population with High Frequency of FV Leiden Mutation by Miklós, T, Oláh, Z, Schlammadinger, Á, Ilonczai, P, Pfliegler, G, Boda, Z, Bernadett Kovács, K, Gindele, R, Szabó, Z, Kerényi, A, Muszbek, L, Bereczky, Z

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Screening and monitoring of the BTKC481S mutation in a real‐world cohort of patients with relapsed/refractory chronic lymphocytic leukaemia during ibrutinib therapy by Bödör, Csaba, Kotmayer, Lili, László, Tamás, Takács, Ferenc, Barna, Gábor, Kiss, Richárd, Sebestyén, Endre, Nagy, Tibor, Hegyi, Lajos László, Mikala, Gábor, Fekete, Sándor, Farkas, Péter, Balogh, Alexandra, Masszi, Tamás, Demeter, Judit, Weisinger, Júlia, Alizadeh, Hussain, Kajtár, Béla, Kohl, Zoltán, Szász, Róbert, Gergely, Lajos, Gurbity Pálfi, Timea, Sulák, Adrienn, Kollár, Balázs, Egyed, Miklós, Plander, Márk, Rejtő, László, Szerafin, László, Ilonczai, Péter, Tamáska, Péter, Pettendi, Piroska, Lévai, Dóra, Schneider, Tamás, Sebestyén, Anna, Csermely, Péter, Matolcsy, András, Mátrai, Zoltán, Alpár, Donát

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Treatment of mantle cell lymphoma with autologous stem-cell transplantation in a patient with severe congenital haemophilia-A and chronic (B and C virus) hepatitis by REJTO, L., SCHLAMMADINGER, A., ILONCZAI, P., TORNAI, I., BATAR, P., REMENYI, GY, KISS, A., UDVARDY, M.

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P050 Successful immune tolerance induction treatment of therapy-resistent acquired haemophilia with high inhibitor titer: a case report by Ilonczai, P, Schlammadinger, Á, Oláh, Zs, Rázsó, K, Bereczky, Zs, Boda, Z

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P052 Low dose factor concentrate prophylaxis in patients with severe haemorrhagic disorders by Schlammadinger, Á, Ilonczai, P, Oláh, Zs, Rázsó, K, Boda, Z

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Low‐burden TP53 mutations represent frequent genetic events in CLL with an increased risk for treatment initiation by László, Tamás, Kotmayer, Lili, Fésüs, Viktória, Hegyi, Lajos, Gróf, Stefánia, Nagy, Ákos, Kajtár, Béla, Balogh, Alexandra, Weisinger, Júlia, Masszi, Tamás, Nagy, Zsolt, Farkas, Péter, Demeter, Judit, Istenes, Ildikó, Szász, Róbert, Gergely, Lajos, Sulák, Adrienn, Borbényi, Zita, Lévai, Dóra, Schneider, Tamás, Pettendi, Piroska, Bodai, Emese, Szerafin, László, Rejtő, László, Bátai, Árpád, Dömötör, Mária Á, Sánta, Hermina, Plander, Márk, Szendrei, Tamás, Hamed, Aryan, Lázár, Zsolt, Pauker, Zsolt, Radványi, Gáspár, Kiss, Adrienn, Körösmezey, Gábor, Jakucs, János, Dombi, Péter J, Simon, Zsófia, Klucsik, Zsolt, Gurzó, Mihály, Tiboly, Márta, Vidra, Tímea, Ilonczai, Péter, Bors, András, Andrikovics, Hajnalka, Egyed, Miklós, Székely, Tamás, Masszi, András, Alpár, Donát, Matolcsy, András, Bödör, Csaba

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OC 17.3 Prothrombotic Polymorphisms FV Leiden and Prothrombin G20210A in 699 Unrelated Patients with Congenital Antithrombin Deficiency: More than a Prognostic Value by Bravo Perez, C., Orlando, C., Gindele, R., Cifuentes, R., Stouffs, K., Ilonczai, P., de la Morena-Barrio, M., Schlammadinger, Á., Pfliegler, G., Corral, J., Jochmans, K., Bereczky, Z.

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P168 Hepatitis B virus reactivation in a case of non-Hodgkin's lymphoma treated with immuno-chemotherapy (including fludarabine and rituximab) by Ujj, Zs, Rejtö, L, Tornai, I, Kiss, A, Telek, B, Reményi, Gy, Ilonczai, P, Udvardy, M

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P049 Could heparin-induced thrombocytopenia and thrombosis be a rare manifestation of antiphospholipid antibody syndrome? by Olah, Z, Schlammadinger, A, Mikita, J, Ilonczai, P, Razso, K, Bereczky, Z, Boda, Z

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P018 Autologous bone marrow-derived stem cell transplantation in severe peripheral arterial disorder: the first five patients in Hungary by Szarvas, M, Rázsó, K, Oláh, Zs, Ilonczai, P, Farkas, K, Tóth, J, Jámbor, L, Soltész, P, Litauszky, K, Hunyadi, J, Sipos, T, Kappelmayer, J, Veréb, Z, Rajnav¨olgyi, É, Boda, Z

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O26 A pilot study with autologous bone marrow-derived stem cell transplantation (ABSCT) in patients with severe peripheral arterial disorder (SPAD) by Boda, Z, Farkas, K, Tóth, J, Jámbor, L, Soltész, P, Rázsó, K, Sipos, T, Szarvas, M, Oláh, Zs, Ilonczai, P, Litauszky, K, Veréb, Z, Rajnav¨olgyi, E

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COULD HEPARIN-INDUCED THROMBOCYTOPENIA AND THROMBOSIS BE A RARE MANIFESTATION OF ANTIPHOSPHOLIPID ANTIBODY SYNDROME? by Oláh, Z., Schlammadinger, A., Mikita, J., Ilonczai, P., Rázsó, K., Bereczky, Z., Boda, Z.

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Treatment of mantle cell lymphoma with autologous stem-cell transplantation in a patient with severe congenital haemophilia-A and chronic (B and C virus) hepatitis by Rejto, L, Schlammadinger, A, Ilonczai, P, Tornai, I, Batar, P, Remenyi, Gy, Kiss, A, Udvardy, M

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