Kateřina Pavelcová - Search Results

Year	Number of Results
2016	1
2017	2
2018	2
2019	4
2020	1
2021	2
2022	3
2023	3
2024	1

1

Novel Somatic UBA1 Variant in a Patient With VEXAS Syndrome.

Stiburkova B, Pavelcova K, Belickova M, Magaziner SJ, Collins JC, Werner A, Beck DB, Balajkova V, Salek C, Vostry M, Mann H, Vencovsky J. Stiburkova B, et al. Among authors: pavelcova k. Arthritis Rheumatol. 2023 Jul;75(7):1285-1290. doi: 10.1002/art.42471. Epub 2023 May 11. Arthritis Rheumatol. 2023. PMID: 36762418

2

Alterations in lipidome profiles distinguish early-onset hyperuricemia, gout, and the effect of urate-lowering treatment.

Kvasnička A, Friedecký D, Brumarová R, Pavlíková M, Pavelcová K, Mašínová J, Hasíková L, Závada J, Pavelka K, Ješina P, Stibůrková B. Kvasnička A, et al. Among authors: pavelcova k. Arthritis Res Ther. 2023 Dec 2;25(1):234. doi: 10.1186/s13075-023-03204-6. Arthritis Res Ther. 2023. PMID: 38042879 Free PMC article.

3

An Unusual Cause of Exercise-Induced Acute Kidney Injury.

Quan V, Ali O, Pavelcova K, Harris F, Stiburkova B. Quan V, et al. Among authors: pavelcova k. Am J Med. 2018 Apr;131(4):e145-e146. doi: 10.1016/j.amjmed.2017.10.053. Epub 2017 Nov 22. Am J Med. 2018. PMID: 29175239 No abstract available.

4

Identification of a dysfunctional exon-skipping splice variant in GLUT9/SLC2A9 causal for renal hypouricemia type 2.

Toyoda Y, Cho SK, Tasic V, Pavelcová K, Bohatá J, Suzuki H, David VA, Yoon J, Pallaiova A, Šaligová J, Nousome D, Cachau R, Winkler CA, Takada T, Stibůrková B. Toyoda Y, et al. Among authors: pavelcova k. Front Genet. 2023 Jan 17;13:1048330. doi: 10.3389/fgene.2022.1048330. eCollection 2022. Front Genet. 2023. PMID: 36733941 Free PMC article.

5

The Examination of a TPMT Gene Before Administration of Azathioprine in Rheumatology Practice and Identification of a Novel Variant p.W29R.

Pavelcova K, Hanova P, Ciferska H, Hasikova L, Stiburkova B. Pavelcova K, et al. J Clin Rheumatol. 2022 Mar 1;28(2):e363-e367. doi: 10.1097/RHU.0000000000001727. J Clin Rheumatol. 2022. PMID: 34870401

6

Functional non-synonymous variants of ABCG2 and gout risk.

Stiburkova B, Pavelcova K, Zavada J, Petru L, Simek P, Cepek P, Pavlikova M, Matsuo H, Merriman TR, Pavelka K. Stiburkova B, et al. Among authors: pavelcova k. Rheumatology (Oxford). 2017 Nov 1;56(11):1982-1992. doi: 10.1093/rheumatology/kex295. Rheumatology (Oxford). 2017. PMID: 28968913

7

The impact of dysfunctional variants of ABCG2 on hyperuricemia and gout in pediatric-onset patients.

Stiburkova B, Pavelcova K, Pavlikova M, Ješina P, Pavelka K. Stiburkova B, et al. Among authors: pavelcova k. Arthritis Res Ther. 2019 Mar 20;21(1):77. doi: 10.1186/s13075-019-1860-8. Arthritis Res Ther. 2019. PMID: 30894219 Free PMC article.

8

Functional Characterization of Rare Variants in OAT1/SLC22A6 and OAT3/SLC22A8 Urate Transporters Identified in a Gout and Hyperuricemia Cohort.

Vávra J, Mančíková A, Pavelcová K, Hasíková L, Bohatá J, Stibůrková B. Vávra J, et al. Among authors: pavelcova k. Cells. 2022 Mar 22;11(7):1063. doi: 10.3390/cells11071063. Cells. 2022. PMID: 35406626 Free PMC article.

9

Renal Hypouricemia 1: Rare Disorder as Common Disease in Eastern Slovakia Roma Population.

Stiburkova B, Bohatá J, Pavelcová K, Tasic V, Plaseska-Karanfilska D, Cho SK, Potočnaková L, Šaligová J. Stiburkova B, et al. Among authors: pavelcova k. Biomedicines. 2021 Nov 3;9(11):1607. doi: 10.3390/biomedicines9111607. Biomedicines. 2021. PMID: 34829836 Free PMC article.

10

Familial early-onset hyperuricemia and gout associated with a newly identified dysfunctional variant in urate transporter ABCG2.

Toyoda Y, Pavelcová K, Klein M, Suzuki H, Takada T, Stiburkova B. Toyoda Y, et al. Among authors: pavelcova k. Arthritis Res Ther. 2019 Oct 28;21(1):219. doi: 10.1186/s13075-019-2007-7. Arthritis Res Ther. 2019. PMID: 31661014 Free PMC article. No abstract available.

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