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
- 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
- Acute kidney injury in two children caused by renal hypouricaemia type 22012 | First Faculty of Medicine
- Diagnostic tests for primary renal hypouricemia2011 | First Faculty of Medicine
- Novel homozygous insertion in SLC2A9 gene caused renal hypouricemia2011 | First Faculty of Medicine
- Unusual presentation of Kelley-Seegmiller syndrome2008 | First Faculty of Medicine, Third Faculty of Medicine
- 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
- Hereditary xanthinuria is not so rare disorder of purine metabolism2018 | First Faculty of Medicine
- Hypouricemia and hyperuricosuria in a pubescent girl: Questions & Answers2018 | First Faculty of Medicine
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