- Genetic analysis of SLC12A3 gene of patients with Gitelman syndrom in the Czech RepublicPublication without faculty affiliation
- Gitelman syndrome: novel mutation and long-term follow-up2012 | First Faculty of Medicine
- DNA Analysis of Renal Electrolyte Transporter Genes Among Patients Suffering from Bartter and Gitelman Syndromes - Summary of Mutation Screening2011 | First Faculty of Medicine
- Gitelman's syndrome as common cause of hypokalemia and hypomagnesemia2016 | First Faculty of Medicine
- Homozygous missense mutation in SLC 12A3 gene caused Gitelmanś syndrome with chondrocalcinosisPublication without faculty affiliation
- Gitelman Syndrome as a Cause of Psychomotor Retardation in a Toddler2013 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Sudden cardiac arrest in a child with Gitelman syndrome: a case report and literature review2023 | Second Faculty of Medicine
- Genetic Analysis of Gitelman Syndrome Patients from the Czech Republic and Slovakia - Three Novel Mutations Found2006 | First Faculty of Medicine, Faculty of Science
- Molecular Patterns Discriminate Accommodation and Subclinical Antibody-mediated Rejection in Kidney Transplantation2019 | First Faculty of Medicine