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Joanna Cielecka-Kuszyk

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Articles 41
Citations 387
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Recent Articles
1.
Kaps-Kopiec D, Wozniak M, Jarzebicka D, Grzywa-Czuba R, Pawlowska J, Czubkowski P, et al.
Pol J Pathol . 2024 Aug; 75(2):153-156. PMID: 39166523
The IgG4-associated autoimmune hepatitis (IgG4-AIH) is a newly proposed disease entity characterised by the accumulation of the IgG4-expressing plasma cells in the liver. Its pathophysiology and clinical significance remain unclear...
2.
Fontes A, Pierson H, Bierla J, Eberhagen C, Kinschel J, Akdogan B, et al.
Metabolism . 2024 Jul; 158:155973. PMID: 38986805
In Wilson disease (WD), liver copper (Cu) excess, caused by mutations in the ATPase Cu transporting beta (ATP7B), has been extensively studied. In contrast, in the gastrointestinal tract, responsible for...
3.
Kaps-Kopiec D, Czajkowska A, Gorska M, Wozniak M, Jarzebicka D, Cielecka-Kuszyk J, et al.
Clin Exp Hepatol . 2023 Jul; 9(2):115-121. PMID: 37502437
Aim Of The Study: The treatment of autoimmune hepatitis (AIH) is based on steroids and azathioprine (AZA). AZA is a pro-drug which is converted among others into 6-thioguanine (6-TG) and...
4.
Lipinski P, Ciara E, Jurkiewicz D, Mekrouda M, Cielecka-Kuszyk J, Jurkiewicz E, et al.
Diagnostics (Basel) . 2023 Jun; 13(11). PMID: 37296768
Introduction: The increasing usage of NGS technology has enabled the discovery of new causal genes in ciliopathies, including the gene. The aim of our study was to present the clinical,...
5.
Majsiak E, Cukrowska B, Choina M, Bielawski K, Cielecka-Kuszyk J, Konopka E, et al.
Nutrients . 2023 Jan; 15(1). PMID: 36615859
The diagnosis of celiac disease (CD) at the first diagnostic step requires the detection of specific class A antibodies to tissue transglutaminase type-2 (TG2 IgA) and the measurement of total...
6.
Janowska M, Bierla J, Kaleta M, Wierzbicka-Rucinska A, Czubkowski P, Kanarek E, et al.
J Clin Med . 2022 Dec; 11(24). PMID: 36555887
The pathogenesis of biliary atresia (BA) is still not clear. The aim of this study was to evaluate the expression of selected immunological parameters in liver tissue in BA children...
7.
Jankowska I, Pawlowska J, Szymczak M, Ismail H, Broniszczak D, Cielecka-Kuszyk J, et al.
Am J Case Rep . 2021 Jul; 22:e932374. PMID: 34283821
BACKGROUND Current treatment options for progressive intrahepatic familial cholestasis type 1 (PFIC-1) comprise ursodeoxycholic acid (UDCA), partial external biliary diversion (PEBD), and liver transplantation (LTx). The role and timing of...
8.
Czubkowski P, Thompson R, Jankowska I, Knisely A, Finegold M, Parsons P, et al.
World J Clin Cases . 2021 May; 9(15):3631-3636. PMID: 34046462
Background: Functioning farnesoid X receptor (FXR; encoded by ) is key to normal bile acid homeostasis. Biallelic mutations in are reported in a few children with intrahepatic cholestasis. We describe...
9.
Cielecka-Kuszyk J, Janowska M, Markiewicz M, Czubkowski P, Ostoja-Chyzynska A, Bierla J, et al.
Clin Exp Hepatol . 2021 May; 7(1):41-46. PMID: 34027114
Aim Of The Study: To assess ductular proliferation (DP) and ductal plate malformation (DPM) in biliary atresia (BA) by means of immunohistochemical staining using cytokeratins CK7 and CK19 and neural...
10.
Lipinski P, Cielecka-Kuszyk J, Czarnowska E, Bogdanska A, Socha P, Tylki-Szymanska A
Pediatr Neonatol . 2021 Mar; 62(3):278-283. PMID: 33663989
Background: Congenital disorders of glycosylation (CDG) result from defects in the synthesis of glycans and their attachment to proteins and lipids. Histologically, liver steatosis, fibrosis and cirrhosis have been reported...