Zobrazeno 1 - 10
of 189
pro vyhledávání: '"Mariusz, Kusztal"'
Autor:
Maciej Gołębiowski, Mariusz Kusztal, MD, PhD, Maciej Szymczak, MD, PhD, Andrzej Konieczny, MD, PhD, Mirosław Banasik, MD, PhD, Dariusz Janczak, MD, PhD, Pierre Bourquelot, MD, PhD, Tomasz Gołębiowski, MD, PhD
Publikováno v:
Journal of Vascular Surgery Cases and Innovative Techniques, Vol 10, Iss 6, Pp 101635- (2024)
The purpose of this manuscript is to describe the clinical course of a 66-year-old patient with chronic kidney disease due to focal segmental glomerulosclerosis in whom an access arteriovenous fistula was created in the anatomical snuffbox. At discha
Externí odkaz:
https://doaj.org/article/0a950a9d6962449188c39158cea937bf
Autor:
Jakub Stojanowski, Andrzej Konieczny, Klaudia Rydzyńska, Izabela Kasenberg, Aleksandra Mikołajczak, Tomasz Gołębiowski, Magdalena Krajewska, Mariusz Kusztal
Publikováno v:
BMC Nephrology, Vol 23, Iss 1, Pp 1-11 (2022)
Abstract Background Lupus nephropathy (LN) occurs in approximately 50% of patients with systemic lupus erythematosus (SLE), and 20% of them will eventually progress into end-stage renal disease (ESRD). A clinical tool predicting remission of proteinu
Externí odkaz:
https://doaj.org/article/3716414aec5a47318ca5d637c657949c
Autor:
Bartlomiej Blaszczyk, Mieszko Wieckiewicz, Mariusz Kusztal, Monika Michalek-Zrabkowska, Gabriella Lachowicz, Grzegorz Mazur, Helena Martynowicz
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
BackgroundFabry disease (FD) is an X-chromosome-linked disorder characterized by a reduced or complete absence of the enzyme α-galactosidase, resulting in the accumulation of lysosomal globotriaosylceramide. Despite the presence of these deposits in
Externí odkaz:
https://doaj.org/article/02c88ac2e5ed4c0aaebf7684f2b40f40
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Although associations of IgA nephropathy (IgAN) and ANCA-associated vasculitis (AAV) have been described, this coexistence scarcely occurs and requires multidisciplinary management. Herein, we discuss a course of treatment introduced in a patient wit
Externí odkaz:
https://doaj.org/article/1698fdd2f8ce42a0bccc61ece9f45b9a
Autor:
Tomasz Gołębiowski, Sławomir Zmonarski, Wiktoria Rożek, Mateusz Powązka, Patryk Jerzak, Maciej Gołębiowski, Mariusz Kusztal, Piotr Olczyk, Jakub Stojanowski, Krzysztof Letachowicz, Mirosław Banasik, Andrzej Konieczny, Magdalena Krajewska
Publikováno v:
Diagnostics, Vol 13, Iss 21, p 3367 (2023)
Background: Normal-anion-gap metabolic acidosis (AGMA) and high-anion-gap metabolic acidosis (HAGMA) are two forms of metabolic acidosis, which is a common complication in patients with chronic kidney disease (CKD). The aim of this study is to identi
Externí odkaz:
https://doaj.org/article/f5feb43aa33749e78b8461aa7765869e
Autor:
Anna Włudarczyk, Grzegorz Biedroń, Krzysztof Wójcik, Zbigniew Zdrojewski, Anna Masiak, Zenobia Czuszyńska, Maria Majdan, Radosław Jeleniewicz, Magdalena Krajewska, Mariusz Kusztal, Marek Brzosko, Iwona Brzosko, Alicja Dębska-Ślizień, Hanna Storoniak, Witold Tłustochowicz, Joanna Kur-Zalewska, Andrzej Rydzewski, Marta Madej, Anna Hawrot-Kawecka, Małgorzata Stasiek, Eugeniusz Kucharz, Jacek Musial, Wojciech Szczeklik
Publikováno v:
Anaesthesiology Intensive Therapy, Vol 52, Iss 4, Pp 281-286 (2020)
Externí odkaz:
https://doaj.org/article/65c32befa2ac4326af9b9b7ccc563e94
Autor:
Michał Nowicki, Monika Komar, Mariusz Kusztal, Katarzyna Mizia-Stec, Tomasz Liberek, Jolanta Małyszko, Katarzyna Muras-Szwedziak, Krzysztof Pawlaczyk, Piotr Podolec, Jarosław Sławek
Publikováno v:
F1000Research, Vol 10 (2021)
Fabry disease (FD) is an ultra-rare genetic lysosomal storage disease caused by pathologic gene variants resulting in insufficient expression of α-galactosidase A. This enzyme deficiency leads to accumulation of globotriaosylceramide and globotriaos
Externí odkaz:
https://doaj.org/article/8f9bce18977c489b93edd6aaf63201e9
Autor:
Tadeusz Fiłon, Łukasz Rogowski, Mariusz Kusztal, Katarzyna Bulińska, Weronika Pawlaczyk, Tomasz Gołębiowski, Agnieszka Zembroń-Łacny, Marian Klinger, Marek Woźniewski, Wioletta Dziubek
Publikováno v:
Physiotherapy Quarterly, Vol 27, Iss 1, Pp 39-45 (2019)
Externí odkaz:
https://doaj.org/article/783b448dab6c444c9e4bd87e5511e765
Autor:
Andrzej Konieczny, Piotr Donizy, Tomasz Gołębiowski, Andrzej Tukiendorf, Agnieszka Hałoń, Mariusz Kusztal, Hanna Augustyniak-Bartosik, Magdalena Krajewska
Publikováno v:
Diagnostics, Vol 11, Iss 10, p 1764 (2021)
IgA nephropathy (IgAN) is the most frequent primary glomerulonephritis worldwide. Due to its heterogenicity, there is a need to establish robust biomarkers for IgAN, to support treatment decisions and evaluate the risk of progression to end-stage ren
Externí odkaz:
https://doaj.org/article/b2a722c8d9094f309162cae192597650
Autor:
Klaudia Bardowska, Krzysztof Letachowicz, Dorota Kamińska, Mariusz Kusztal, Tomasz Gołębiowski, Tomasz Królicki, Karolina Zajdel, Oktawia Mazanowska, Dariusz Janczak, Magdalena Krajewska
Publikováno v:
PLoS ONE, Vol 15, Iss 7, p e0234931 (2020)
BACKGROUND:Arteriovenous fistulas (AVF) are a source of various complications. Among previously hemodialyzed kidney transplant recipients (KTxR), the AVF may persist over time. The patients' decisions whether to ligate the functioning AVF may be prom
Externí odkaz:
https://doaj.org/article/4e67076b28394bfeaf7949c227d5ede4