Publikace
- Gitelman Syndrome as a Cause of Psychomotor Retardation in a Toddler2013 | 1. lékařská fakulta, Lékařská fakulta v Hradci Králové
- DNA Analysis of Renal Electrolyte Transporter Genes Among Patients Suffering from Bartter and Gitelman Syndromes - Summary of Mutation Screening2011 | 1. lékařská fakulta
- Mutation Screening for patients with Gitelman Syndrom in the Czech Republic. 2 novel mutations foundPublikace bez příslušnosti k fakultě
- Ambulatory blood pressure and hypertension control in children with autosomal recessive polycystic kidney disease: clinical experience from two central European tertiary centres2022 | 1. lékařská fakulta, 2. lékařská fakulta, Fakulta tělesné výchovy a sportu
- Improvement of Diagnostic Yield by an Additional Amplicon Module to Hybridization-Based Next-Generation Sequencing Panels2022 | 1. lékařská fakulta
- Results of targeted next-generation sequencing in children with cystic kidney diseases often change the clinical diagnosis2020 | 1. lékařská fakulta, 2. lékařská fakulta
- Two Czech patients with familial adenomatous polyposis presenting mosaicism in APC gene2019 | 1. lékařská fakulta
- Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease - a case report2018 | 1. lékařská fakulta
- Mutational screening of inverted formin 2 in adult-onset focal segmental glomerulosclerosis or minimal change patients from the Czech Republic2018 | 1. lékařská fakulta
- Molekulární onkologie v kasuistikách2017 | 1. lékařská fakulta, 3. lékařská fakulta
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