Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Monika, Drogosiewicz"'
Autor:
Marta Perek-Polnik, Anne Cochrane, Jinli Wang, Marzanna Chojnacka, Monika Drogosiewicz, Iwona Filipek, Ewa Swieszkowska, Magdalena Tarasinska, Wiesława Grajkowska, Joanna Trubicka, Paweł Kowalczyk, Bożenna Dembowska-Bagińskai, Mohamed S. Abdelbaki
Publikováno v:
Children, Vol 10, Iss 8, p 1387 (2023)
Craniospinal irradiation (CSI) has been a major component of the standard of care treatment backbone for childhood medulloblastoma. However, chemotherapy regimens have varied based on protocol, patient age, and molecular subtyping. In one of the larg
Externí odkaz:
https://doaj.org/article/a75953c573114ef189665756af983ec1
Autor:
Kornelia Łach, Aneta Kowal, Marta Perek-Polnik, Paweł Jakubczyk, Christopher J. Arthur, Wioletta Bal, Monika Drogosiewicz, Bożenna Dembowska-Bagińska, Wiesława Grajkowska, Józef Cebulski, Radosław Chaber
Publikováno v:
Molecules, Vol 28, Iss 5, p 2390 (2023)
Introduction: Medulloblastoma (MB) is the most common malignant tumor of the central nervous system in childhood. FTIR spectroscopy provides a holistic view of the chemical composition of biological samples, including the detection of molecules such
Externí odkaz:
https://doaj.org/article/5a0e851340a84fd48a720acaf9e035a4
Autor:
Joanna Trubicka, Tomasz Żemojtel, Jochen Hecht, Katarzyna Falana, Dorota Piekutowska- Abramczuk, Rafał Płoski, Marta Perek-Polnik, Monika Drogosiewicz, Wiesława Grajkowska, Elżbieta Ciara, Elżbieta Moszczyńska, Bożenna Dembowska-Bagińska, Danuta Perek, Krystyna H. Chrzanowska, Małgorzata Krajewska-Walasek, Maria Łastowska
Publikováno v:
BMC Cancer, Vol 17, Iss 1, Pp 1-11 (2017)
Abstract Background The defects in DNA repair genes are potentially linked to development and response to therapy in medulloblastoma. Therefore the purpose of this study was to establish the spectrum and frequency of germline variants in selected DNA
Externí odkaz:
https://doaj.org/article/a96162f4796c4a65bf39ef853fbba71b
Publikováno v:
Neuro-Oncology. 24:i58-i58
BACKGROUND: Central nervous system (CNS) germinoma relapses are rare. However, the latest Children’s Oncology Group (COG), ACNS1123 stratum 2, described three relapses along the biopsy tract out of eight total relapses; two along the biopsy and end
Autor:
Wojciech MŁynarski, Walentyna Balwierz, Katarzyna PawiŃska-WĄsikowska, Anna Raciborska, Agata MarjaŃska, Mariusz Wysocki, Katarzyna Bobeff, BoŻenna Dembowska-BagiŃska, Agnieszka Mizia-Malarz, Monika Drogosiewicz, Jan StyczyŃski
Publikováno v:
Anticancer research. 40(12)
Background/aim Nivolumab is an immune checkpoint inhibitor with high antitumor activity in selected neoplasms. The aim of the study was to evaluate the efficacy and safety of nivolumab in pediatric patients with various types of highly malignant adva
Autor:
Adam Kretowski, Bożena Cukrowska, Magdalena Paczkowska-Abdulsalam, Ewa Matyja, Agnieszka Karkucinska-Wieckowska, Magdalena Niemira, Maria Łastowska, Magdalena Kaleta, Marta Perek-Polnik, Bożenna Dembowska-Bagińska, Wiesława Grajkowska, Joanna Trubicka, Monika Drogosiewicz
Publikováno v:
Journal of Neuro-Oncology
Medulloblastoma, the most common malignant pediatric brain tumor, is a heterogeneous disease, with the existence of at least four molecular types: Wingless (WNT), Sonic Hedgehog (SHH), Group 3 and Group 4 tumors. The latter two groups, which can be i
Autor:
Ewa Matyja, Magdalena Tarasińska, Monika Drogosiewicz, Wiesława Grajkowska, Joanna Trubicka, Adam Kretowski, Marta Perek-Polnik, Magdalena Kaleta, Maciej Pronicki, Maria Łastowska, Magdalena Paczkowska-Abdulsalam, Agnieszka Karkucinska-Wieckowska, Bożenna Dembowska-Bagińska, Magdalena Niemira
Publikováno v:
ResearcherID
ALK gene rearrangements were identified in a variety of cancers, including neuroblastoma, where the presence of ALK expression is associated with adverse prognosis. ALK mutations have recently been found in the pediatric brain tumor medulloblastoma,
Autor:
Krystyna H. Chrzanowska, Małgorzata Krajewska-Walasek, Katarzyna Falana, Marta Perek-Polnik, Elżbieta Moszczyńska, Dorota Piekutowska-Abramczuk, Wiesława Grajkowska, Danuta Perek, Monika Drogosiewicz, Joanna Trubicka, Elżbieta Ciara, Jochen Hecht, Bożenna Dembowska-Bagińska, Rafał Płoski, Tomasz Żemojtel, Maria Łastowska
Publikováno v:
BMC Cancer, Vol 17, Iss 1, Pp 1-11 (2017)
BMC Cancer
BMC Cancer
Background The defects in DNA repair genes are potentially linked to development and response to therapy in medulloblastoma. Therefore the purpose of this study was to establish the spectrum and frequency of germline variants in selected DNA repair g
Autor:
Halldora K. Thorarinsdottir, Geert O. Janssens, Ella Kumirova, Sophie E. M. Veldhuijzen van Zanten, Ulrich W. Thomale, Ingrid Torsvik, Virve Pentikäinen, Victor Calvagna, N. Harry Hendrikse, Giedre Rutkauskiene, Veronica Biassoni, Dannis G. van Vuurden, Vicente Santa-Maria Lopez, Fatma E El-Khouly, Maria Joao Gil-da-Costa, Stefan Holm, Simon Bailey, Kaie Pruunsild, Monika Drogosiewicz, Ofelia Cruz-Martinez, Jacques Grill, Gertjan J.L. Kaspers, Maura Massimino, David Sumerauer, Jane Pears, Peter Hauser, Lidija Kitanovski, G. Loizos, Christof M. Kramm, André O. von Bueren, Natacha Entz-Werle, Monica Dragomir, Antonis Kattamis, Karsten Nysom, Tim Hayden, Ladislav Deak, Irene Slavc, Rejin Kebudi, Sandra Jacobs, Enrique López Aguilar, Filip Jadrijevic-Cvrlje
Publikováno v:
Journal of Neuro-Oncology, 145(1), 177. Kluwer Academic Publishers
Journal of Neuro-Oncology
Journal of Neuro-Oncology, 145(1), 177-184. Kluwer Academic Publishers
el-Khouly, F E, Veldhuijzen van Zanten, S E M, Santa-Maria Lopez, V, Hendrikse, N H, Kaspers, G J L, Loizos, G, Sumerauer, D, Nysom, K, Pruunsild, K, Pentikainen, V, Thorarinsdottir, H K, Rutkauskiene, G, Calvagna, V, Drogosiewicz, M, Dragomir, M, Deak, L, Kitanovski, L, von Bueren, A O, Kebudi, R, Slavc, I, Jacobs, S, Jadrijevic-Cvrlje, F, Entz-Werle, N, Grill, J, Kattamis, A, Hauser, P, Pears, J, Biassoni, V, Massimino, M, Lopez Aguilar, E, Torsvik, I K, Joao Gil-da-Costa, M, Kumirova, E, Cruz-Martinez, O, Holm, S, Bailey, S, Hayden, T, Thomale, U W, Janssens, G O R, Kramm, C M & van Vuurden, D G 2019, ' Diagnostics and treatment of diffuse intrinsic pontine glioma : where do we stand? ', Journal of Neuro-Oncology, vol. 145, no. 1, pp. 177-184 . https://doi.org/10.1007/s11060-019-03287-9, https://doi.org/10.1007/s11060-019-03287-9
Journal of neuro-oncology, Vol. 145, No 1 (2019) pp. 177-184
Journal of Neuro-Oncology
Journal of Neuro-Oncology, 145(1), 177-184. Kluwer Academic Publishers
el-Khouly, F E, Veldhuijzen van Zanten, S E M, Santa-Maria Lopez, V, Hendrikse, N H, Kaspers, G J L, Loizos, G, Sumerauer, D, Nysom, K, Pruunsild, K, Pentikainen, V, Thorarinsdottir, H K, Rutkauskiene, G, Calvagna, V, Drogosiewicz, M, Dragomir, M, Deak, L, Kitanovski, L, von Bueren, A O, Kebudi, R, Slavc, I, Jacobs, S, Jadrijevic-Cvrlje, F, Entz-Werle, N, Grill, J, Kattamis, A, Hauser, P, Pears, J, Biassoni, V, Massimino, M, Lopez Aguilar, E, Torsvik, I K, Joao Gil-da-Costa, M, Kumirova, E, Cruz-Martinez, O, Holm, S, Bailey, S, Hayden, T, Thomale, U W, Janssens, G O R, Kramm, C M & van Vuurden, D G 2019, ' Diagnostics and treatment of diffuse intrinsic pontine glioma : where do we stand? ', Journal of Neuro-Oncology, vol. 145, no. 1, pp. 177-184 . https://doi.org/10.1007/s11060-019-03287-9, https://doi.org/10.1007/s11060-019-03287-9
Journal of neuro-oncology, Vol. 145, No 1 (2019) pp. 177-184
Introduction Diffuse intrinsic pontine glioma (DIPG) is a rare clinically, neuro-radiologically, and molecularly defined malignancy of the brainstem with a median overall survival of approximately 11 months. Our aim is to evaluate the current tendenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56c4a1c7159536c1bc0c8d610250afc1
https://dspace.library.uu.nl/handle/1874/391428
https://dspace.library.uu.nl/handle/1874/391428
Autor:
Iwona Filipek, Paweł Kowalczyk, Elżbieta Jurkiewicz, Wiesława Grajkowska, Monika Drogosiewicz, Bożenna Dembowska-Bagińska, Marta Perek-Polnik, Ewa Swieszkowska
INTRODUCTION: Pineoblastoma is a rare, highly aggressive supratentorial tumour, more frequently diagnosed in young children. The prognosis remains poor. AIM: To present own experience with children with pineoblastoma. PATIENTS AND METHODS: 14 pts: 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afc1816c41a355c70577730bf452cd97
https://europepmc.org/articles/PMC6012540/
https://europepmc.org/articles/PMC6012540/