Publications
- Identification of Two Dysfunctional Variants in the ABCG2 Urate Transporter Associated with Pediatric-Onset of Familial Hyperuricemia and Early-Onset Gout2021 | First Faculty of Medicine
- Functional non-synonymous variants of ABCG2 and gout risk2017 | Faculty of Physical Education and Sport, First Faculty of Medicine
- The Examination of a TPMT Gene Before Administration of Azathioprine in Rheumatology Practice and Identification of a Novel Variant p.W29R2022 | First Faculty of Medicine
- Evaluation of the Influence of Genetic Variants ofSLC2A9(GLUT9) andSLC22A12(URAT1) on the Development of Hyperuricemia and Gout2020 | First Faculty of Medicine, Faculty of Mathematics and Physics
- Functional Characterization of Clinically-Relevant Rare Variants in ABCG2 Identified in a Gout and Hyperuricemia Cohort2019 | First Faculty of Medicine, Faculty of Science, Faculty of Mathematics and Physics, Central Library of Charles University
- Interaction of the p.Q141K Variant of the ABCG2 Gene with Clinical Data and Cytokine Levels in Primary Hyperuricemia and Gout2019 | First Faculty of Medicine, Faculty of Science, Faculty of Mathematics and Physics
- The impact of dysfunctional variants of ABCG2 on hyperuricemia and gout in pediatric-onset patients2019 | Faculty of Physical Education and Sport, First Faculty of Medicine
- Familial early-onset hyperuricemia and gout associated with a newly identified dysfunctional variant in urate transporter ABCG22019 | First Faculty of Medicine
- An Unusual Cause of Exercise-Induced Acute Kidney Injury2018 | Faculty of Physical Education and Sport, First Faculty of Medicine
- Thiopurine-induced toxicity is associated with dysfunction variant of the human molybdenum cofactor sulfurase gene (xanthinuria type II)2018 | First Faculty of Medicine
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