Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Anna, Wakulińska"'
Autor:
Magdalena Kaleta, Anna Wakulińska, Agnieszka Karkucińska-Więckowska, Bożenna Dembowska-Bagińska, Wiesława Grajkowska, Maciej Pronicki, Maria Łastowska
Publikováno v:
Diagnostic Pathology, Vol 14, Iss 1, Pp 1-7 (2019)
Abstract Background The most frequent histological types of rhabdomyosarcoma (RMS) in children are embryonal (ERMS) and alveolar (ARMS) tumours. The majority of ARMS are characterized by the presence of PAX3/7-FOXO1 gene fusion and have a worse progn
Externí odkaz:
https://doaj.org/article/b5f414a50ed24d0fbd961e73b690e4d5
Autor:
Katarzyna Bąbol-Pokora, Ewa Bernatowska, Nel Dąbrowska-Leonik, Maciej Dądalski, Bożenna Dembowska-Bagińska, Katarzyna Drabko, Katarzyna Grzela, Edyta Heropolitańska-Pliszka, Sylwia Kołtan, Aleksandra Lewandowicz-Uszyńska, Bożena Mikołuć, Małgorzata Pac, Barbara Piątosa, Barbara Pietrucha, Anna Wakulińska, Beata Wolska-Kuśnierz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::215b999a4035c2dca9b36bb0af2d658b
https://doi.org/10.53271/2022.106
https://doi.org/10.53271/2022.106
Autor:
Karl-Walter Sykora, Larysa Kostyuchenko, Jolanta Gozdzik, Bożena Dembowska-Bagińska, Peter Svec, Sara Sebnem Kilic, Barbara Pietrucha, Ewa Więsik-Szewczyk, Katarzyna Drabko, Michael H. Albert, Hanna Gregorek, Beata Wolska-Kusnierz, Barbara Piątosa, Mary Eapen, Alexandra Y. Kreins, Wojciech Młynarski, Agata Pastorczak, Krystyna H. Chrzanowska, Sylwia Kołtan, Dmitry Balashov, Agnieszka Tomaszewska, Zdenka Krenova, Monika Lejman, Natalia Miakova, Marek Ussowicz, E.V. Deripapa, Edyta Heropolitańska-Pliszka, Bendik Lund, Anna Wakulińska, Eva Hlaváčková, Johann Greil, Markus G. Seidel, Sujal Ghosh, Anna Pieczonka, Alina Fedorova, Jochen Buechner, Jan Styczyński, Krzysztof Kałwak, Wojciech Fendler, Andrew R. Gennery
Purpose: Nijmegen breakage syndrome (NBS) is a DNA repair disorder with a high predisposition to hematologic malignancies. Experimental Design: We describe the natural history of NBS, including cancer incidence, risk of death, and the potential effec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4edb2e4f4669d49b7255e530b9cf1288
https://ruj.uj.edu.pl/xmlui/handle/item/267421
https://ruj.uj.edu.pl/xmlui/handle/item/267421
Autor:
Katarzyna Tkaczyk, Anna Wakulińska, Hanna Gregorek, Beata Wolska-Kuśnierz, Barbara Piatosa, Urszula Grycuk, Edyta Heropolitańska-Pliszka
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Frontiers in Immunology
Frontiers in Immunology
Patients with Nijmegen Breakage Syndrome (NBS) suffer from recurrent infections due to humoral and cellular immune deficiency. Despite low number of T lymphocytes and their maturation defect, the clinical manifestations of cell-mediated deficiency ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dd683b978c0974f449259a55668fa46
Autor:
Joanna Teisseyre, Iwona Daniluk, Ryszard Grenda, Anna Wakulińska, Bożenna Dembowska-Bagińska, Wiesława Grajkowska, Wioletta Jarmużek, Irena Jankowska, Piotr Kaliciński, Jagoda Maldyk, Piotr Czubkowski
Publikováno v:
Advances in clinical and experimental medicine : official organ Wroclaw Medical University. 29(2)
Background Post-transplantation lymphoproliferative disorder (PTLD) is a complication of organ transplantation and a life-threatening condition. Children who underwent organ transplantation are at risk of developing lymphoproliferative disorders and,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::036b9be845a818e08a0d83b551a67529
https://pubmed.ncbi.nlm.nih.gov/32154678
https://pubmed.ncbi.nlm.nih.gov/32154678
Autor:
Krystyna H. Chrzanowska, Hanna Gregorek, Dorota Piekutowska-Abramczuk, Anna Wakulińska, Dominika Smolka-Afifi, Beata Kasztelewicz, Małgorzata Pac, Magdalena Zborowska, Anna Zapaśnik, Katarzyna Dzierżanowska-Fangrat, Jadwiga Małdyk, Barbara Pietrucha
Publikováno v:
Clinical Immunology. 135:440-447
Selected viruses and immune parameters were monitored in 57 patients with Nijmegen breakage syndrome as a proposed tool for early detection of changes preceding development of malignancy. The following parameters were analysed: (1) viral infections;
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cf8c6d6e07f084f14b9d457bdeac7ae
https://doi.org/10.1016/j.clim.2010.01.008
https://doi.org/10.1016/j.clim.2010.01.008
Autor:
Małgorzata Gładkowska-Dura, Wiesława Grajkowska, Agnieszka Brozyna, Dorota Olczak-Kowalczyk, Danuta Perek, Anna Wakulińska, Krystyna H. Chrzanowska, Bożenna Dembowska-Bagińska
Publikováno v:
Pediatric Blood & Cancer. 52:186-190
Background Due to small number of patients with Nijmegen Breakage Syndrome (NBS) and Non-Hodgkin lymphoma (NHL) experience in their treatment is limited. Procedure Since 1996, 17 patients with a median age of 9.5 years who had NBS, were treated for N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63461a1a4265f626f23a783690150ae1
https://doi.org/10.1002/pbc.21789
https://doi.org/10.1002/pbc.21789
Autor:
Sara Sebnem Kilic, Krystyna H. Chrzanowska, Peter Čižnar, Anna Shcherbina, Michael H. Albert, Barbara Pietrucha, Larysa Kostyuchenko, Małgorzata Syczewska, Ulrich Baumann, Srdjan Pasic, Małgorzata Pac, Anna Wakulińska, Hanna Gregorek, Krzysztof Kałwak, Anna Pieczonka, Bernd H. Belohradsky, Edyta Heropolitańska-Pliszka, Jan Styczyński, Barbara Piątosa, Andrew R. Gennery, Katarzyna Drabko, Ewa Bernatowska, Urszula Skarżyńska, Markus G. Seidel, Maja Klaudel-Dreszler, László Maródi, Beata Wolska-Kuśnierz, Bożena Mikołuć, Benjamin Gathmann
Publikováno v:
Journal of clinical immunology. 35(6)
Nijmegen Breakage Syndrome (NBS) is a rare inherited condition, characterized by microcephaly, chromosomal instability, immunodeficiency, and predisposition to malignancy. This retrospective study, characterizing the clinical and immunological status
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f239a32f9ad23667ed98ad16d09429bd
https://pubmed.ncbi.nlm.nih.gov/26271390
https://pubmed.ncbi.nlm.nih.gov/26271390
Autor:
Teresa Luszawska-Kutrzeba, Bozenna Goryluk-Kozakiewicz, Halina Bubała, Katarzyna Stefańska, Andrzej Kołtan, Jadwiga Małdyk, Marta Kuźmicz, Lucyna Maciejka-Kapuścińska, Małgorzata Syczewska, Małgorzata Stolarska, Bernarda Kazanowska, Artur Gadomski, Anna Wakulińska, Ewa Popowska, Małgorzata Krajewska-Walasek, Katarzyna Sznurkowska, Anna Gaworczyk, Jerzy Kowalczyk, Krystyna H. Chrzanowska, Małgorzata Gładkowska-Dura, Maria Wieczorek, Dorota Piekutowska-Abramczuk, Tomasz Szczepański
Publikováno v:
International Journal of Cancer. 118:1269-1274
Nijmegen breakage syndrome (NBS) is a human autosomal recessive disease characterized by genomic instability and enhanced cancer predisposition, in particular to lymphoma and leukemia. Recently, significantly higher frequencies of heterozygous carrie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dbb91cee1c2b1abc30aebdc09b64423
https://doi.org/10.1002/ijc.21439
https://doi.org/10.1002/ijc.21439
Autor:
Richard A. Gatti, Barbara Pietrucha, Anna Wakulińska, Edyta Heropolitańska-Pliszka, Hanna Skopczynska, Ewa Bernatowska
Publikováno v:
Journal of Pediatric Hematology/Oncology. 32:e28-e30
SUMMARY Ataxia-telangiectasia is an autosomal recessive disorder caused by mutation in the ATM gene. Hallmarks of the disease comprise progressive cerebellar ataxia, oculocutaneous telangiectasiae, cancer susceptibility, and variable humoral and cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74e5f843a0180f13ce4bc4a9c4afe9b6
https://doi.org/10.1097/mph.0b013e3181bfd3d9
https://doi.org/10.1097/mph.0b013e3181bfd3d9