Publikace
- Functional non-synonymous variants of ABCG2 and gout risk2017 | 1. lékařská fakulta, Fakulta tělesné výchovy a sportu
- Modern diagnostic approach to hereditary xanthinuria2015 | 1. lékařská fakulta
- High frequency of SLC22A12 variants causing renal hypouricemia 1 in the Czech and Slovak Roma population; simple and rapid detection method by allele-specific polymerase chain reaction2015 | 1. lékařská fakulta
- Complex Analysis of Urate Transporters SLC2A9, SLC22A12 and Functional Characterization of Non-Synonymous Allelic Variants of GLUT9 in the Czech Population: No Evidence of Effect on Hyperuricemia and Gout2014 | 1. lékařská fakulta, Přírodovědecká fakulta
- Diagnostický test primární renální hypourikémie.2011 | 1. lékařská fakulta
- Interleukin-37: associations of plasma levels and genetic variants in gout2023 | 1. lékařská fakulta, Matematicko-fyzikální fakulta
- Alterations in lipidome profiles distinguish early-onset hyperuricemia, gout, and the effect of urate-lowering treatment2023 | 1. lékařská fakulta, Matematicko-fyzikální fakulta
- Identification of a dysfunctional exon-skipping splice variant in GLUT9/SLC2A9 causal for renal hypouricemia type 22023 | 1. lékařská fakulta
- Association of Gout Polygenic Risk Score With Age at Disease Onset and Tophaceous Disease in European and Polynesian Men With Gout2023 | 1. lékařská fakulta
- Novel Somatic UBA1 Variant in a Patient With VEXAS Syndrome2023 | 1. lékařská fakulta
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