Classes
- Biochemistry 1 DB00178 | First Faculty of Medicine
- Biochemistry 2 DB00530 | First Faculty of Medicine
- Renovating businessB01599 | First Faculty of Medicine
- Blood sampling techniqueB01607 | First Faculty of Medicine
- Case studies from laboratory diagnosticsB02089 | First Faculty of Medicine
- Clinical biochemistry 1B02568 | First Faculty of Medicine
- Clinical biochemistry 2B02588 | First Faculty of Medicine
- Inovating BusinessB81599 | First Faculty of Medicine
- Blood Sampling TechniquesB81607 | First Faculty of Medicine
Publications
- Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis2013 | First Faculty of Medicine, Third Faculty of Medicine, Faculty of Science
- Genetic Disorders Resulting in Hyper- or Hypouricemia2012 | First Faculty of Medicine
- Novel mutations in xanthine dehydrogenase/oxidase cause severe hypouricemia: Biochemical and molecular genetic analysis in two Czech families with xanthinuria type I2012 | First Faculty of Medicine
- Diagnostic tests for primary renal hypouricemia2011 | First Faculty of Medicine
- Polymorphisms of the TPMT gene in the Czech healthy population and patients with inflammatory bowel disease2008 | First Faculty of Medicine
- Diagnostic importance of uric acid2005 | First Faculty of Medicine
- Partial deficiency of HGPRT in a girlPublication without faculty affiliation
- Familial juvenile hyperuricemic nephropathy (FJHN): Localization of the gene on chromosome 16P11. 2 and evidence for genetic heterogenityPublication without faculty affiliation
- Analysis of Purine Metabolism to Elucidate the Pathogenesis of Acute Kidney Injury in Renal Hypouricemia2022 | First Faculty of Medicine
- Modified forearm ischemic test in hypouricemic patients2020 | First Faculty of Medicine
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