Katerina Pavelcova
8PUBLICATIONS
20CO-AUTHORS
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Publications (8)
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|Aug 22, 2025
Diagnostic performance of four proposed algorithms for suspected VEXAS syndrome.Tereza Sychrovská, Blanka Stibůrková, Kateřina Pavelcová
|Mar 14, 2025
Identification of pathogenic variants in the ABCG2 gene in patients with severe familial hyperuricemia and gout.Yu Toyoda, Katerina Pavelcova, Jana Masinova
|Jan 15, 2024
Examining the Association of Rare Allelic Variants in Urate Transporters SLC22A11, SLC22A13, and SLC17A1 with Hyperuricemia and Gout.Jiří Vávra, Kateřina Pavelcová, Jana Mašínová
|Dec 02, 2023
Alterations in lipidome profiles distinguish early-onset hyperuricemia, gout, and the effect of urate-lowering treatment.Aleš Kvasnička, David Friedecký, Radana Brumarová
|Apr 12, 2022
Functional Characterization of Rare Variants in OAT1/SLC22A6 and OAT3/SLC22A8 Urate Transporters Identified in a Gout and Hyperuricemia Cohort.Jiří Vávra, Andrea Mančíková, Kateřina Pavelcová
|Nov 27, 2021
Renal Hypouricemia 1: Rare Disorder as Common Disease in Eastern Slovakia Roma Population.Blanka Stiburkova, Jana Bohatá, Kateřina Pavelcová
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Frequent Collaborators
7 joint publications
Jana Mašínová
7 joint publications
Blanka Stiburkova
4 joint publications
Lenka Hasíková
2 joint publications
Yu Toyoda
2 joint publications
Tappei Takada
2 joint publications
Jiří Vávra
2 joint publications
Jakub Závada
1 joint publications
Velibor Tasic
1 joint publications
Dijana Plaseska-Karanfilska
1 joint publications
Jana Šaligová
