Zobrazeno 1 - 10
of 86
pro vyhledávání: '"Ewa Gorczyńska"'
Autor:
Justyna Miśkiewicz-Bujna, Izabella Miśkiewicz-Migoń, Zofia Szmit, Dawid Przystupski, Monika Rosa, Anna Król, Krzysztof Kałwak, Marek Ussowicz, Ewa Gorczyńska
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
IntroductionAllogeneic hematopoietic stem cell transplantation (allo-HSCT) is a treatment method for a wide range of malignant and non-malignant diseases. Infants constitute a distinct patient group, especially due to their organ immaturity and diffe
Externí odkaz:
https://doaj.org/article/7c7d451e6f5d4646850eac60a8cc6ef2
Autor:
Tomasz Jarmoliński, Monika Rosa, Blanka Rybka, Renata Ryczan-Krawczyk, Kornelia Gajek, Katarzyna Bogunia-Kubik, Maja Klaudel-Dreszler, Piotr Czubkowski, Piotr Kaliciński, Joanna Teisseyre, Marek Stefanowicz, Ewa Gorczyńska, Krzysztof Kałwak, Marek Ussowicz
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
We report a child with Fanconi anemia who, after hematopoietic stem cell transplantation (HSCT) complicated by acute graft-versus-host disease (GVHD), underwent orthotopic liver transplantation (OLT). Approximately 1 month after OLT, the presence of
Externí odkaz:
https://doaj.org/article/efdd36937e9e4d6ebbb0036ef6b7f6e1
Autor:
Paweł Marschollek, Karolina Liszka, Monika Mielcarek-Siedziuk, Blanka Rybka, Renata Ryczan-Krawczyk, Anna Panasiuk, Igor Olejnik, Jowita Frączkiewicz, Iwona Dachowska-Kałwak, Agnieszka Mizia-Malarz, Tomasz Szczepański, Wojciech Młynarski, Jan Styczyński, Katarzyna Drabko, Grażyna Karolczyk, Ewa Gorczyńska, Jan Maciej Zaucha, Krzysztof Kałwak
Publikováno v:
Biomedicines, Vol 10, Iss 11, p 2915 (2022)
The optimal bridging therapy before CAR-T cell infusion in pediatric relapsed or refractory B-cell precursor acute lymphoblastic leukemia (r/r BCP-ALL) still remains an open question. The administration of blinatumomab prior to CAR-T therapy is contr
Externí odkaz:
https://doaj.org/article/59ce3a5d070e430689de72587b548172
Autor:
Izabella Miśkiewicz-Migoń, Justyna Miśkiewicz-Bujna, Monika Mielcarek-Siedziuk, Jowita Frączkiewicz, Ewa Gorczyńska, Krzysztof Kałwak
Publikováno v:
Pediatria Polska, Vol 96, Iss 1, Pp 68-70 (2021)
Krabbe disease (KD) is a lysosomal storage disorder, caused by a deficiency of galactocerebrosidase (GALC) or a mutation in the prosaposin gene, which leads to psychosine accumulation. Consequently, demyelination and degradation of the nervous system
Externí odkaz:
https://doaj.org/article/42e24dde5fb642cf88902753f7a31817
Autor:
Mariusz Wysocki, Krzysztof Czyżewski, Dorota Sęga-Pondel, Bernarda Kazanowska, Jolanta Goździk, Małgorzata Salamonowicz-Bodzioch, Jacek Wachowiak, Ewa Gorczyńska, Jadwiga Węcławek-Tompol, Jerzy Kowalczyk, Magdalena Dziedzic, Krzysztof Kałwak, Jowita Frączkiewicz, Jan Styczyński, Grażyna Wróbel, Marek Ussowicz, Agnieszka Zaucha-Prażmo, Olga Zając-Spychała
Publikováno v:
Annals of Hematology
The aim of this multi-center study was to evaluate the incidence, clinical course, and risk factors for bacterial multidrug-resistant (MDR) gastrointestinal tract infections (GTI) among children undergoing allogeneic and autologous hematopoietic cell
Autor:
Zofia Szmit, Jowita Frączkiewicz, Małgorzata Salamonowicz-Bodzioch, Anna Król, Marek Ussowicz, Monika Mielcarek-Siedziuk, Karolina Liszka, Paweł Marschollek, Ewa Gorczyńska, Krzysztof Kałwak
Publikováno v:
Journal of Clinical Medicine; Volume 11; Issue 17; Pages: 5187
Hematopoietic stem cell transplantation (HSCT) is a curative therapy for an increasing number of nonmalignant indications. Its use is restricted by severe transplant-related complications, including CMV infection; despite various prophylactic and the
Autor:
Monika Mielcarek-Siedziuk, Ewa Gorczyńska, Karolina Liszka, Paweł Marschollek, Krzysztof Kałwak, Joanna Taha, Blanka Rybka
Publikováno v:
Acta Haematologica Polonica. 52:211-213
When all of the usually applied treatment methods fail, we have to try something innovative. In this vignette, we present the history of the first in Poland CAR-T cell therapy in a child with refractory B-cell acute lymphoblastic leukemia (ALL). In m
Autor:
Aneta Gietka, Bernarda Kazanowska, Grażyna Sobol-Milejska, Maryna Krawczuk-Rybak, Krzysztof Czyżewski, Łukasz Hutnik, K. Kałwak, Katarzyna Dzierżanowska-Fangrat, Jacek Wachowiak, Elżbieta Drożyńska, Marcin Płonowski, Grażyna Karolczyk, Bożenna Dembowska-Bagińska, Alicja Chybicka, Jerzy Kowalczyk, Olga Zając-Spychała, Jowita Frączkiewicz, Anna Pieczonka, Zuzanna Gamrot-Pyka, Weronika Stolpa, Ewa Bien, Agnieszka Urbanek-Dądela, Jan Styczyński, Mariola Woszczyk, Filip Pierlejewski, Katarzyna Semczuk, Anna Szmydki-Baran, Grażyna Wróbel, Ninela Irga-Jaworska, Ewa Gorczyńska, Wojciech Młynarski, Małgorzata Salamonowicz, Patrycja Zalas-Więcek, Olga Gryniewicz-Kwiatkowska, Magdalena Dziedzic, M. Matysiak, Mariusz Wysocki, Jolanta Goździk, Agnieszka Zaucha-Prażmo
Publikováno v:
Journal of Medical Virology. 92:3187-3193
The aim was to evaluate the incidence, clinical course, and outcome of adenoviral infection (AdVI) in pediatric patients diagnosed and treated due to cancer and in pediatric recipients of hematopoietic stem cell. Over a 72-month period, all-in 5599 c
Autor:
Marek Ussowicz, Ewa Gorczyńska, Igor Olejnik, Anna Panasiuk, Zofia Szmit, Anna Król, Monika Mielcarek-Siedziuk, Krzysztof Kałwak
Publikováno v:
Bone Marrow Transplantation. 55:2138-2146
Hepatic veno-occlusive disease (VOD) is a potentially fatal complication following hematopoietic stem cell transplantation (HSCT). We evaluated in prospective analysis the usefulness of the pediatric EBMT criteria for VOD diagnosis and their presumab
Autor:
Tomasz Jarmoliński, Anna Panasiuk, Krzysztof Kałwak, Marek Ussowicz, Małgorzata Salamonowicz-Bodzioch, Blanka Rybka, Igor Olejnik, Małgorzata Janeczko-Czarnecka, Jowita Frączkiewicz, Joanna Owoc-Lempach, Renata Ryczan-Krawczyk, Kornelia Gajek, Monika Rosa, Monika Mielcarek-Siedziuk, Ewa Gorczyńska, Katarzyna Gul
Publikováno v:
Journal of Clinical Medicine
Volume 10
Issue 19
Journal of Clinical Medicine, Vol 10, Iss 4416, p 4416 (2021)
Volume 10
Issue 19
Journal of Clinical Medicine, Vol 10, Iss 4416, p 4416 (2021)
Severe aplastic anemia (SAA) is a bone marrow failure syndrome that can be treated with hematopoietic cell transplantation (HCT) or immunosuppressive (IS) therapy. A retrospective cohort of 56 children with SAA undergoing transplantation with fludara