Mariusz Kusztal
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Explore the profile of Mariusz Kusztal including associated specialties, affiliations and a list of published articles.
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108
Citations
446
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Recent Articles
1.
Golebiowski M, Chumadevska M, Kusztal M, Banasik M, Golebiowski T
Case Rep Nephrol Dial
. 2025 Jan;
15(1):9-14.
PMID: 39845264
Introduction: A common complication of arteriovenous fistula (AVF) is thrombosis in the venous segment, which can impair vascular access unless a successful thrombectomy is performed. Case Presentation: In this manuscript,...
2.
Podolec P, Mitkowski P, Slowik A, Gala-Bladzinska A, Gancarczyk U, Gil R, et al.
Kardiol Pol
. 2025 Jan;
83(2):231-253.
PMID: 39743907
Fabry disease (FD) belongs to the group of lysosomal storage diseases (LSD), characterized by insufficient enzyme activity responsible for the intra-lysosomal breakdown of various substrates. The result is an uncontrolled...
3.
Golebiowski M, Kusztal M, Szymczak M, Konieczny A, Banasik M, Janczak D, et al.
J Vasc Surg Cases Innov Tech
. 2024 Nov;
10(6):101635.
PMID: 39497931
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...
4.
Golebiowski T, Zmonarski S, Rozek W, Powazka M, Jerzak P, Golebiowski M, et al.
Diagnostics (Basel)
. 2023 Nov;
13(21).
PMID: 37958263
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...
5.
Golebiowski T, Kusztal M, Konieczny A, Golebiowski M, Letachowicz K, Janczak D, et al.
J Clin Med
. 2023 Oct;
12(20).
PMID: 37892619
Background: The most common form of vascular access for hemodialysis is a native arteriovenous fistula, which connects the site of the artery to the end of the vein. The maturation...
6.
Blaszczyk B, Wieckiewicz M, Kusztal M, Michalek-Zrabkowska M, Lachowicz G, Mazur G, et al.
Front Neurol
. 2023 Oct;
14:1217618.
PMID: 37869133
Background: Fabry 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...
7.
Tota M, Donizy P, Byrska M, Krajewska M, Kusztal M
Front Immunol
. 2023 Aug;
14:1227878.
PMID: 37649475
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...
8.
Stojanowski J, Konieczny A, Lis L, Frosztega W, Brzozowska P, Ciszewska A, et al.
J Clin Med
. 2023 Jul;
12(14).
PMID: 37510869
The majority of recently published studies indicate a greater incidence and mortality due to infection (CDI) in patients with chronic kidney disease (CKD). Hospitalization, older age, the use of antibiotics,...
9.
Szymczak A, Kusztal M, Golebiowski T, Letachowicz K, Gozdzik A, Koscielska-Kasprzak K, et al.
Int J Mol Sci
. 2023 Jun;
24(12).
PMID: 37373181
Volume status, congestion, endothelial activation, and injury all play roles in glomerular filtration rate (GFR) decline. In this study, we aimed to determine whether the plasma endothelial and overhydration markers...
10.
Tota M, Baron V, Musial K, Derrough B, Konieczny A, Krajewska M, et al.
J Clin Med
. 2023 Apr;
12(7).
PMID: 37048809
Primary (pIgAN), secondary IgA nephropathy (sIgAN), and IgA-associated nephropathy can be distinguished. While pIgAN has been thoroughly studied, information about the etiology of sIgAN remains scarce. As concerns sIgAN, several...