Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Katalin, Bartyik"'
Autor:
Barbara Vodicska, Júlia Déri, Dóra Tihanyi, Edit Várkondi, Enikő Kispéter, Róbert Dóczi, Dóra Lakatos, Anna Dirner, Mátyás Vidermann, Péter Filotás, Réka Szalkai-Dénes, István Szegedi, Katalin Bartyik, Krisztina Míta Gábor, Réka Simon, Péter Hauser, György Péter, Csongor Kiss, Miklós Garami, István Peták
Publikováno v:
World Journal of Pediatrics.
Autor:
Erika Biró, Dániel Erdélyi, Petra Varga, Mária Sinkó, Katalin Bartyik, Gábor Kovács, Gábor Ottóffy, Ferenc Vincze, István Szegedi, Csongor Kiss, Tamás Szabó
Publikováno v:
Pediatric Nephrology.
Background Tumor lysis syndrome (TLS) and its most serious complication, acute kidney injury (AKI) are one of the emergency conditions in onco-hematology. It is difficult to predict the degree of kidney involvement. Therefore, we studied children wit
Autor:
Barbara Vodicska, Júlia Déri, Dóra Tihanyi, Edit Várkondi, Enikő Kispéter, Róbert Dóczi, Dóra Lakatos, Anna Dirner, Mátyás Vidermann, Péter Filotás, Réka Szalkai-Dénes, István Szegedi, Katalin Bartyik, Krisztina Míta Gábor, Réka Simon, Péter Hauser, György Péter, Csongor Kiss, Miklós Garami, István Peták
Publikováno v:
World Journal of Pediatrics.
Background The utility of routine extensive molecular profiling of pediatric tumors is a matter of debate due to the high number of genetic alterations of unknown significance or low evidence and the lack of standardized and personalized decision sup
Autor:
Miklós Garami, György Péter, Marianna Zombori, Katalin Bartyik, Peter Hauser, Ágnes Vojcek, Zsuzsanna Jakab, Dániel J. Erdélyi, Attila Juhász, Judit Müller, Monika Csóka, Gabor G. Kovacs, Csilla Nagy, Gergely Kriván, Edit Bardi, István Szegedi, Péter Masát, Imre Rényi, Agnes Kelemen
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-9 (2020)
Scientific Reports
Scientific Reports
The Hungarian Pediatric Oncology Network provides centralized treatment and population-based registration for cases of childhood cancer since 1973. We collected and analized data on late mortality, secondary malignancies and cardiac diseases in survi
Autor:
Péter Masát, Gábor Ottóffy, Blanka Tóth, Katalin Bartyik, Marienn Réti, Csaba Kassa, Réka Simon, Emma Ádám, György Péter, Gergely Kriván, Judit Csomor, Csongor Kiss, Krisztián Kállay, Gabor G. Kovacs, Csaba Bödör
Publikováno v:
Orvosi Hetilap. 159:1710-1719
Abstract: Introduction: Acquired bone marrow failures are rare but fatal diseases in childhood. Since 2013, Hungary has been participating as a full member in the work of the European Working Group on uniform diagnostics and therapy in patients with
Publikováno v:
Gyermekgyógyászat; 2022, Vol. 73 Issue 1, p28-35, 8p
Publikováno v:
Journal of Cancer Education
The aim of this study was to compare the quality of life and school success of adolescent survivors and their classmates. A survey was conducted among 21 cancer survived 12-18-year-old children and 95 of their classmates by using questionnaires cover
Autor:
B. Vodicska, R. Simon, P. Filotas, Peter Hauser, Miklós Garami, E. Várkondi, István Szegedi, J. Deri, C. Hegedues, György Péter, István Peták, Csongor Kiss, Dora Tihanyi, Krisztina Mita Gabor, Katalin Bartyik
Publikováno v:
Annals of Oncology. 31:S1103
[Change in paradigm in the treatment of pediatric acquired bone marrow failure syndromes in Hungary]
Autor:
Krisztián, Kállay, Judit, Csomor, Emma, Ádám, Csaba, Bödör, Csaba, Kassa, Réka, Simon, Gábor, Kovács, György, Péter, Gábor, Ottóffy, Katalin, Bartyik, Csongor, Kiss, Péter, Masát, Marienn, Réti, Blanka, Tóth, Gergely, Kriván
Publikováno v:
Orvosi hetilap. 159(42)
Acquired bone marrow failures are rare but fatal diseases in childhood. Since 2013, Hungary has been participating as a full member in the work of the European Working Group on uniform diagnostics and therapy in patients with acquired bone marrow fai
Autor:
Gábor Benyó, Tibor Hortobágyi, Peter Hauser, Petra Mózes, László Bognár, István Peták, Katalin Hideghéty, Adrienne Cserháti, Zoltán Nagy, Katalin Bartyik, Eszter Turányi, Miklós Garami
Publikováno v:
Journal of Neuro-Oncology. 126:99-105
The embryonal tumor with abundant neuropil and true rosettes is a rare and highly malignant variant of embryonal brain tumors. It usually affects infants and young children under the age of 4 years and exhibits a very aggressive course with a dismal