Zobrazeno 1 - 10
of 130
pro vyhledávání: '"Maciej Pronicki"'
Autor:
Piotr Socha, Elizabeth Shumbayawonda, Abhishek Roy, Caitlin Langford, Paul Aljabar, Malgorzata Wozniak, Sylwia Chełstowska, Elzbieta Jurkiewicz, Rajarshi Banerjee, Ken Fleming, Maciej Pronicki, Kamil Janowski, Wieslawa Grajkowska
Publikováno v:
Journal of Pathology Informatics, Vol 15, Iss , Pp 100372- (2024)
Background: Chronic liver disease diagnoses depend on liver biopsy histopathological assessment. However, due to the limitations associated with biopsy, there is growing interest in the use of quantitative digital pathology to support pathologists. W
Externí odkaz:
https://doaj.org/article/2b86709eac224c63bd682dda77183019
Autor:
Joanna Trubicka, Maria Łastowska, Agnieszka Karkucińska-Więckowska, Magdalena Niemira, Maria Ejmont, Agnieszka Sowińska, Maciej Pronicki, Ewa Matyja, Wiesława Grajkowska
Publikováno v:
Folia Neuropathologica, Vol 61, Iss 2, Pp 121-128 (2023)
BCOR is expressed in a new brain tumour entity, i.e. ‘CNS tumour with BCOR internal tandem duplication’ (HGNET BCOR) but not in several other high grade paediatric brain tumours investigated. Immunohistochemical detection of BCOR expression may t
Externí odkaz:
https://doaj.org/article/a8029630c0e24ea59e0970ff420734b2
Autor:
Maria Łastowska, Ewa Matyja, Anna Sobocińska, Bartosz Wojtaś, Magdalena Niemira, Anna Szałkowska, Adam Krętowski, Agnieszka Karkucińska‐Więckowska, Magdalena Kaleta, Maria Ejmont, Magdalena Tarasińska, Marta Perek‐Polnik, Bożenna Dembowska‐Bagińska, Maciej Pronicki, Wiesława Grajkowska, Joanna Trubicka
Publikováno v:
The Journal of Pathology: Clinical Research, Vol 7, Iss 6, Pp 565-576 (2021)
Abstract The majority of supratentorial ependymomas in children contain oncogenic fusions, such as ZFTA–RELA or YAP1‐MAMLD1. In contrast, posterior fossa (PF) ependymomas lack recurrent somatic mutations and are classified based on gene expressio
Externí odkaz:
https://doaj.org/article/7e8570c907ad436eb02c29b0dbf990be
Autor:
Patryk Lipiński, Elżbieta Ciara, Dorota Jurkiewicz, Maciej Pronicki, Elżbieta Jurkiewicz, Anna Bogdańska, Rafał Płoski, Irena Jankowska
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Adenosine kinase (ADK) deficiency is a rare inborn error of methionine and adenosine metabolism. So far, a total of 27 patients with ADK deficiency have been reported. Here, we describe the first Polish patient diagnosed with ADK deficiency, aiming t
Externí odkaz:
https://doaj.org/article/fcbd64df5adf4defb90d4f6a0510d73d
Autor:
Kamil Janowski, Elizabeth Shumbayawonda, Lin Cheng, Caitlin Langford, Andrea Dennis, Matt Kelly, Maciej Pronicki, Wieslawa Grajkowska, Malgorzata Wozniak, Piotr Pawliszak, Sylwia Chełstowska, Elzbieta Jurkiewicz, Rajarshi Banerjee, Piotr Socha
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Abstract Autoimmune hepatitis (AIH) and autoimmune sclerosing cholangitis (ASC) are two very closely related autoimmune liver diseases with overlapping clinical features and similar management strategies. The purpose of this study was to assess the u
Externí odkaz:
https://doaj.org/article/a5ec93bb818648ec974d64986e5ca604
Autor:
Joanna Radzikowska, Anna M. Czarnecka, Teresa Klepacka, Magdalena Rychłowska-Pruszyńska, Anna Raciborska, Bożenna Dembowska-Bagińska, Maciej Pronicki, Andrzej Kukwa, Wojciech Fendler, Urszula Smyczyńska, Wojciech Kukwa, Antoni Krzeski
Publikováno v:
Diagnostics, Vol 12, Iss 8, p 1895 (2022)
(1) Background: The aim of the present study was to assess the cancer stem cell (CSC) markers CD24, CD44, CD133, and ALDH1A1 in rhabdomyosarcoma (RMS) in children and to define their prognostic role in this group of patients. (2) Methods: The study m
Externí odkaz:
https://doaj.org/article/037038de60b74c25bced0d00718b4174
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:
Maciej Pronicki, Dorota Piekutowska-Abramczuk, Dariusz Rokicki, Katarzyna Iwanicka-Pronicka, Wiesława Grajkowska
Publikováno v:
Polish Journal of Pathology, Vol 69, Iss 3, Pp 292-298 (2018)
Mitochondrial DNA depletion consisting of the systemic reduction of mtDNA copy number in cells may have a heterogenous genetic basis, resulting from a pathogenic change in the nuclear genes involved in mtDNA synthesis. The mode of inheritance is auto
Externí odkaz:
https://doaj.org/article/d48519232d2e481dadce4a589edfd244
Autor:
Kamil Janowski, Elizabeth Shumbayawonda, Matt Kelly, Carlos Ferreira, Maciej Pronicki, Wieslawa Grajkowska, Magdalena Naorniakowska, Piotr Pawliszak, Sylwia Chełstowska, Elżbieta Jurkiewicz, Rajarshi Banerjee, Piotr Socha
Publikováno v:
Children, Vol 9, Iss 5, p 613 (2022)
Wilson disease (WD) is a liver disorder characterized by improper copper metabolism. Although non-invasive tools are currently used to support diagnosis and management, this is still an area of unmet need, as patients present with a wide range of sym
Externí odkaz:
https://doaj.org/article/57f7b542669345fd862e23863821c53d
Autor:
Małgorzata Pac, Teresa Bielecka, Katarzyna Grzela, Justyna Komarnicka, Renata Langfort, Sylwia Koltan, Nel Dabrowska-Leonik, Katarzyna Bernat-Sitarz, Maciej Pronicki, Hanna Dmenska, Anna Pituch-Noworolska, Bozena Mikoluc, Barbara Piatosa, Katarzyna Tkaczyk, Ewa Bernatowska, Irena Wojsyk-Banaszak, Katarzyna Krenke
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Primary immunodeficiencies (PIDs) are rare disorders of the immune system encompassing inborn errors of immunity. Primary antibody deficiencies constitute the largest group of PID with common variable immunodeficiency (CVID) being the most common sym
Externí odkaz:
https://doaj.org/article/daf6269df88d42b3a216d1d2676769cf