Zobrazeno 1 - 10
of 106
pro vyhledávání: '"Stanisława Bazan‑Socha"'
Autor:
Michał Nowicki, Stanisława Bazan-Socha, Beata Błażejewska-Hyżorek, Mariusz M. Kłopotowski, Monika Komar, Mariusz A. Kusztal, Tomasz Liberek, Jolanta Małyszko, Katarzyna Mizia-Stec, Zofia Oko-Sarnowska, Krzysztof Pawlaczyk, Piotr Podolec, Jarosław Sławek, on behalf of the Polish Fabry Disease Collaborative Group
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-13 (2024)
Abstract Fabry disease (FD) is a rare, X-linked lysosomal storage disorder affecting both males and females caused by genetic abnormalities in the gene encoding the enzyme α-galactosidase A. FD-affected patients represent a highly variable clinical
Externí odkaz:
https://doaj.org/article/6eb1ebc51ef24c4782f51c05363cee95
Autor:
Joanna Kosałka-Węgiel, Radosław Dziedzic, Andżelika Siwiec-Koźlik, Magdalena Spałkowska, Mamert Milewski, Anita Wach, Lech Zaręba, Stanisława Bazan-Socha, Mariusz Korkosz
Publikováno v:
Journal of Clinical Medicine, Vol 13, Iss 15, p 4486 (2024)
Background: Lupus nephritis (LN) is an inflammation of the kidneys that is related to systemic lupus erythematosus (SLE). This study aimed to evaluate the differences in clinical and laboratory characteristics between LN and non-LN SLE patients. Meth
Externí odkaz:
https://doaj.org/article/bfc01cce02bb493796d776ea5719e645
Autor:
Anna Drynda, Agnieszka Padjas, Krzysztof Wójcik, Radosław Dziedzic, Grzegorz Biedroń, Katarzyna Wawrzycka-Adamczyk, Anna Włudarczyk, Joanna Wilańska, Jacek Musiał, Zbigniew Zdrojewski, Zenobia Czuszyńska, Anna Masiak, Maria Majdan, Radosław Jeleniewicz, Hanna Augustyniak-Bartosik, Katarzyna Jakuszko, Magdalena Krajewska, Alicja Dębska-Ślizień, Hanna Storoniak, Barbara Bułło-Piontecka, Witold Tłustochowicz, Joanna Kur-Zalewska, Małgorzata Wisłowska, Piotr Głuszko, Marta Madej, Ewa Jassem, Iwona Damps-Konstańska, Eugeniusz Kucharz, Marek Brzosko, Marcin Milchert, Anna Hawrot-Kawecka, Joanna Miłkowska-Dymanowska, Paweł Górski, Anna Lewandowska-Polak, Joanna Makowska, Joanna Zalewska, Lech Zaręba, Stanisława Bazan-Socha
Publikováno v:
Journal of Immunology Research, Vol 2024 (2024)
Objective. To characterize the eosinophilic granulomatosis with polyangiitis (EGPA) population from the POLVAS registry depending on ANCA status and diagnosis onset, including their comparison with the granulomatosis with polyangiitis (GPA) subset wi
Externí odkaz:
https://doaj.org/article/3c451bd1a4a243f987db683b069b20da
Autor:
Radosław Dziedzic, Lech Zaręba, Teresa Iwaniec, Agnieszka Kubicka-Trząska, Bożena Romanowska-Dixon, Stanisława Bazan-Socha, Jerzy Dropiński
Publikováno v:
Thrombosis Journal, Vol 21, Iss 1, Pp 1-11 (2023)
Abstract Introduction Central retinal artery occlusion (CRAO) is a common cause of blindness and visual morbidity. In the majority of cases, it is related to thrombotic embolism. Nevertheless, the role of inherited or acquired thrombophilic risk fact
Externí odkaz:
https://doaj.org/article/028c7be561814e3aa094ac82d90431a3
Autor:
Michał Nowicki, Stanisława Bazan‑Socha, Beata Błażejewska‑Hyżorek, Mariusz M. Kłopotowski, Monika Komar, Mariusz A. Kusztal, Tomasz Liberek, Jolanta Małyszko, Katarzyna Mizia‑Stec, Zofia Oko‑Sarnowska, Krzysztof Pawlaczyk, Piotr Podolec, Jarosław Sławek, the Polish Fabry Disease Collaborative Group
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-1 (2024)
Externí odkaz:
https://doaj.org/article/8a68e492c4d34c71bfc04cdc9626e3ae
Autor:
Dorota Mizera, Radosław Dziedzic, Anna Drynda, Ada Gradzikiewicz, Bogdan Jakieła, Magdalena Celińska-Löwenhoff, Agnieszka Padjas, Aleksandra Matyja-Bednarczyk, Lech Zaręba, Stanisława Bazan-Socha
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
IntroductionPrimary antibody deficiencies (PAD) are inborn defects of the immune system that result in increased susceptibility to infections. Despite the reduced response to vaccination, PAD patients still benefit from it by reducing the risk of sev
Externí odkaz:
https://doaj.org/article/6cc8d69dd96b44a6bb65fd692625de58
Autor:
Stanisława Bazan-Socha, Ada Gradzikiewicz, Magdalena Celińska-Lowenhoff, Aleksandra Matyja-Bednarczyk, Anna Maciołek, Katarzyna Bąbol-Pokora
Publikováno v:
Central European Journal of Immunology, Vol 47, Iss 1, Pp 92-94 (2022)
We present a case of a white adult female patient who suffered from chronic mucocutaneous candidiasis (CMC) since infancy. Her parents were not consanguineous, and neither of them nor any other family member, including an older sister, suffered from
Externí odkaz:
https://doaj.org/article/2cde783032c343dfbdf475bed51a76d1
Autor:
Adrian A. Michalski, Karol Lis, Joanna Stankiewicz, Sylwester M. Kloska, Arkadiusz Sycz, Marek Dudziński, Katarzyna Muras-Szwedziak, Michał Nowicki, Stanisława Bazan-Socha, Michal J. Dabrowski, Grzegorz W. Basak
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 10, p 3599 (2023)
In clinical practice, the consideration of non-specific symptoms of rare diseases in order to make a correct and timely diagnosis is often challenging. To support physicians, we developed a decision-support scoring system on the basis of retrospectiv
Externí odkaz:
https://doaj.org/article/994dde7595b14d5c931be5c763d3134b
Autor:
Stanisława Bazan-Socha, Bogdan Jakieła
Publikováno v:
Biomedicines, Vol 11, Iss 2, p 268 (2023)
In recent years, substantial progress has been made in our understanding of asthma pathomechanisms, especially phenotyping [...]
Externí odkaz:
https://doaj.org/article/c9896043a6a54b978f5ec20a07ca2e42
Autor:
Renata Pacholczak-Madej, Piotr Kuszmiersz, Stanisława Bazan-Socha, Joanna Kosałka-Węgiel, Teresa Iwaniec, Lech Zaręba, Stan Kielczewski, Anna Rams, Jerzy A. Walocha, Jacek Musiał, Jerzy Dropiński
Publikováno v:
Advances in Dermatology and Allergology, Vol 37, Iss 4, Pp 495-502 (2020)
Externí odkaz:
https://doaj.org/article/47e5483a6e854856a4528025f86b3382