Items where Author is "Ilonczai, Péter"
Group by: Item Type | No Grouping Jump to: Article Number of items: 9. ArticleLászló, Tamás and Kotmayer, Lili and Fésüs, Viktória and Hegyi, Lajos and Gróf, Stefánia and Nagy, Ákos and Kajtár, Béla and Balogh, Alexandra and Weisinger, Júlia and Masszi, Tamás and Nagy, Zsolt and Farkas, Péter and Demeter, Judit and Istenes, Ildikó and Szász, Róbert and Gergely, Lajos and Sulák, Adrienn and Borbényi, Zita and Lévai, Dóra and Schneider, Tamás and Pettendi, Piroska and Bódai, Emese and Szerafin, László and Rejtő, László and Bátai, Árpád and Dömötör, Mária and Sánta, Hermina and Plander, Márk and Szendrei, Tamás and Hamed, Aryan and Lázár, Zsolt and Pauker, Zsolt and Radványi, Gáspár and Kiss, Adrienn and Körösmezey, Gábor and Jakucs, János and Dombi, Péter and Simon, Zsófia and Klucsik, Zsolt and Gurzó, Mihály and Tiboly, Márta and Vidra, Tímea and Ilonczai, Péter and Bors, András and Andrikovics, Hajnalka and Egyed, Miklós and Székely, Tamás and Masszi, András and Alpár, Donát and Matolcsy, András and Bödör, Csaba (2024) Low-burden TP53 mutations represent frequent genetic events in CLL with an increased risk for treatment initiation. The Journal of Pathology: Clinical Research. Bödör, Csaba and Kotmayer, Lili and László, Tamás and Takács, Ferenc and Barna, Gábor and Kiss, Richárd and Sebestyén, Endre and Nagy, Tibor and Hegyi, Lajos and Mikala, Gábor and Fekete, Sándor and Farkas, Péter and Balogh, Alexandra and Masszi, Tamás and Demeter, Judit and Weisinger, Júlia and Alizadeh, Hussain and Kajtár, Béla and Kohl, Zoltán and Szász, Róbert and Gergely, Lajos and Gurbity Pálfi, Tímea and Sulák, Adrienn and Kollár, Balázs and Egyed, Miklós and Plander, Márk and Rejtő, László and Szerafin, László and Ilonczai, Péter and Tamáska, Péter and Pettendi, Piroska and Lévai, Dóra and Schneider, Tamás and Sebestyén, Anna and Csermely, Péter and Matolcsy, András and Mátrai, Zoltán and Alpár, Donát (2021) Screening and monitoring of the BTK C481S mutation in a real-world cohort of patients with relapsed/refractory chronic lymphocytic leukaemia during ibrutinib therapy. BRITISH JOURNAL OF HAEMATOLOGY, 194 (2). pp. 355-364. ISSN 0007-1048 (print); 1365-2141 (online) de la Morena-Barrio, Maria E. and Gindele, Réka and Bravo-Perez, Carlos and Ilonczai, Péter and Zuazu, Isabel and Speker, Marianna and Oláh, Zsolt and Rodriguez-Sevilla, Juan J. and Entrena, Laura and Infante, Maria Stefania and de la Morena-Barrio, Belen and Garcia, Jose M. and Schlammadinger, Ágota and Cifuentes-Riquelme, Rosa and Mora-Casado, Asuncion and Minano, Antonia and Padilla, Jose and Vicente, Vicente and Corral, Javier and Bereczky, Zsuzsanna (2021) High penetrance of inferior vena cava system atresia in severe thrombophilia caused by homozygous antithrombin Budapest 3 variant: Description of a new syndrome. AMERICAN JOURNAL OF HEMATOLOGY, 96 (11). pp. 1363-1373. ISSN 0361-8609 Kovács, Andrea and Tajti, Balázs and Szoboszlay, István and Bereczky, Zsuzsanna and Ilonczai, Péter (2021) A szerzett haemophilia A sikeres kezelése. ORVOSI HETILAP, 162 (49). pp. 1977-1981. ISSN 0030-6002 Magyari, Ferenc and Bedekovics, Judit and Décsy, Judit and Ilonczai, Péter and Illés, Árpád and Simon, Zsófia (2018) A korai/praefibroticus primer myelofibrosis kivizsgálása és kezelése egy eset kapcsán = Investigation and treatment of prefibrotic/early primary myelofibrosis. A case study. Orvosi Hetilap, 159 (15). pp. 603-609. ISSN 0030-6002 Gindele, Réka and Selmeczi, Anna and Oláh, Zsolt and Ilonczai, Péter and Pfliegler, György and Marján, Erzsébet and Nemes, László and Nagy, Ágnes and Losonczy, Hajna and Mitic, Gorana and Kovac, Mirjana and Balogh, Gábor and Komáromi, István and Schlammadinger, Ágota and Rázsó, Katalin and Boda, Zoltán and Muszbek, László and Bereczky, Zsuzsanna (2017) Clinical and laboratory characteristics of antithrombin deficiencies: A large cohort study from a single diagnostic center. THROMBOSIS RESEARCH, 160. pp. 119-128. ISSN 0049-3848 Gindele, Réka and Oláh, Zsolt and Ilonczai, Péter and Speker, Marianna and Udvari, A and Selmeczi, A and Pfliegler, György and Marján, E and Kovács, Bettina Erzsébet and Boda, Zoltán and Muszbek, László and Bereczky, Zsuzsanna (2016) Founder effect is responsible for the p.Leu131Phe heparin-binding-site antithrombin mutation common in Hungary: phenotype analysis in a large cohort. JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 14 (4). pp. 704-715. ISSN 1538-7933 Boda, Zoltán and Udvardy, Miklós and Farkas, Katalin and Tóth, Judit and Jámbor, László and Soltész, Pál and Rázsó, Katalin and Oláh, Zsolt and Ilonczai, Péter and Szarvas, Mariann and Litauszky, Krisztina and Hunyadi, János and Sipos, Tamás and Kappelmayer, János and Veréb, Zoltán and Rajnavölgyi, Éva (2008) Autológ csontvelői eredetű őssejtterápia eredménye előrehaladott perifériás artériás érbetegségben = A pilot study with autologous bone marrow-derived stem cell therapy in patients with severe peripheral arterial disorder. Orvosi Hetilap, 149 (12). pp. 531-540. ISSN 0030-6002 Mikita, János and Ilonczai, Péter and Tóth, Judit (2007) Lokális thrombolyticus kezelés perifériás artériás érbetegségben = Local thrombolysis in the treatment of peripheral arterial vascular diseases. Orvosi Hetilap, 148 (37). pp. 1737-1744. ISSN 0030-6002 (print); 1788-6120 (online) |