Blanka Stibůrková (B Stiburkova, Blanka Stiburkova)

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 14

Top Topics

Ankylosing Spondylitis

Allogeneic Hematopoietic Stem Cell Transplantation

Top Venues

Arthritis & rheumatology (Hoboken, N.J.)

Disease markers

Nucleosides, nucleotides & nucleic acids

This page only lists publications with an associated author ORCID identifier.

Publications

Lenka Hasikova, Josef Bartl, Blanka Stibůrková
Urinary oxypurinol is a useful tool to assess adherence to allopurinol in clinical practice. Rheumatology (Oxford, England) 63 (6) (2024)
Jiří Vávra, Kateřina Pavelcová, Jana Mašínová, Lenka Hasikova, Eliška Bubeníková, Aneta Urbanová, Andrea Mančíková, Blanka Stibůrková
Examining the Association of Rare Allelic Variants in Urate Transporters SLC22A11 , SLC22A13 , and SLC17A1 with Hyperuricemia and Gout. Disease markers 2024 (2024)
Jiří Vávra, Kateřina Pavelcová, Jana Mašínová, Lenka Hasikova, Eliška Bubeníková, Aneta Urbanová, Andrea Mančíková, Blanka Stibůrková
Examining the Association of Rare Allelic Variants in Urate Transporters SLC22A11 , SLC22A13 , and SLC17A1 with Hyperuricemia and Gout. Disease markers 2024 (2024)
Jiří Vávra, Kateřina Pavelcová, Jana Mašínová, Lenka Hasikova, Eliška Bubeníková, Aneta Urbanová, Andrea Mančíková, Blanka Stibůrková
Examining the Association of Rare Allelic Variants in Urate Transporters SLC22A11 , SLC22A13 , and SLC17A1 with Hyperuricemia and Gout. Disease markers 2024 (2024)
Blanka Stibůrková, Katerina Pavelcova, Monika Belickova, Samuel J Magaziner, Jason C Collins, Achim Werner, David B Beck, Veronika Balajkova, Cyril Salek, Martin Vostry, Herman Mann, Jiri Vencovsky
Novel somatic UBA1 variant in a patient with VEXAS syndrome. Arthritis & rheumatology (Hoboken, N.J.) (2023)
Aleš Kvasnička, David Friedecký, Radana Brumarová, Markéta Pavlíková, Kateřina Pavelcová, Jana Mašínová, Lenka Hasikova, Jakub Závada, Karel Pavelka, Pavel Ješina, Blanka Stibůrková
Alterations in lipidome profiles distinguish early-onset hyperuricemia, gout, and the effect of urate-lowering treatment. Arthritis research & therapy 25 (1) (2023)
Blanka Stibůrková, Katerina Pavelcova, Monika Belickova, Samuel J Magaziner, Jason C Collins, Achim Werner, David B Beck, Veronika Balajkova, Cyril Salek, Martin Vostry, Herman Mann, Jiri Vencovsky
Novel somatic UBA1 variant in a patient with VEXAS syndrome. Arthritis & rheumatology (Hoboken, N.J.) (2023)
Nicholas A Sumpter, Riku Takei, Murray Cadzow, Ruth K G Topless, Amanda J Phipps-Green, Rinki Murphy, Janak de Zoysa, Huti Watson, Muhammad Qasim, Alexa S Lupi, Abhishek Abhishek, Mariano Andrés, Tania O Crișan, Michael Doherty, Lennart Jacobsson, Matthijs Janssen, Tim L Jansen, Leo A B Joosten, Meliha Crnkic Kapetanovic, Frédéric Lioté, Hirotaka Matsuo, Geraldine M McCarthy, Fernando Perez-Ruiz, Philip Riches, Pascal Richette, Flavia M Cicuttini, Blanka Stibůrková, Alexander So, Anne-Kathrin Tausche, Rosa J Torres, Till Uhlig, Tanya J Major, Lisa K Stamp, Nicola Dalbeth, Hyon K Choi, Ana I Vazquez, Megan P Leask, Richard J Reynolds, Tony Raymond Merriman
Association of Gout Polygenic Risk Score with Age at Disease Onset and Tophaceous Disease in European and Polynesian Men with Gout. Arthritis & rheumatology (Hoboken, N.J.) (2022)
Jiří Vávra, Andrea Mančíková, Kateřina Pavelcová, Lenka Hasikova, Jana Mašínová, Blanka Stibůrková
Functional Characterization of Rare Variants in OAT1/ SLC22A6 and OAT3/ SLC22A8 Urate Transporters Identified in a Gout and Hyperuricemia Cohort. Cells 11 (7) (2022)
Yu Toyoda, Kateřina Pavelcová, Jana Mašínová, Pavel Ješina, Yu Kubota, Hiroshi Suzuki, Tappei Takada, Blanka Stibůrková
Identification of Two Dysfunctional Variants in the ABCG2 Urate Transporter Associated with Pediatric-Onset of Familial Hyperuricemia and Early-Onset Gout. International journal of molecular sciences 22 (4) (2021)
Blanka Stibůrková, Jana Mašínová, Kateřina Pavelcová, Velibor Tasic, Dijana Plaseska-Karanfilska, Sung-Kweon Cho, Ludmila Potočnaková, Jana Šaligová
Renal Hypouricemia 1: Rare Disorder as Common Disease in Eastern Slovakia Roma Population. Biomedicines 9 (11) (2021)
Ivan Sebesta, Daisuke Miyamoto, Blanka Stibůrková, Sarka Blahova, Nana Sato, Koji Nagata, Ken Okamoto, Shuichi Tsuruoka, Kimiyoshi Ichida
Modified forearm ischemic test in hypouricemic patients. Nucleosides, nucleotides & nucleic acids 39 (10-12) (2020)
Lenka Hasikova, Markéta Pavlíková, Hana Hulejová, Petr Kozlík, Kveta Kalikova, Aparna Mahajan, Martin Herrmann, Blanka Stibůrková, Jakub Závada
Serum uric acid increases in patients with systemic autoimmune rheumatic diseases after 3 months of treatment with TNF inhibitors. Rheumatology international 39 (10) (2019)
I Sebesta, Blanka Stibůrková, J Krijt
Hereditary xanthinuria is not so rare disorder of purine metabolism. Nucleosides, nucleotides & nucleic acids 37 (6) (2018)