- Gitelman´s syndrome +12006 | First Faculty of Medicine
- Mutation analysis in Bartter and Gitelman syndrome in Czech republicPublication without faculty affiliation
- Bartter and Gitelman syndromes2022 | Second Faculty of Medicine
- Gitelman Syndrome as a Cause of Psychomotor Retardation in a Toddler2013 | Faculty of Medicine in Hradec Králové, First Faculty of Medicine
- Gitelman syndrome in pregnancy - a severe hypokalemia with favorable perinatal prognosis2012 | Faculty of Medicine in Pilsen
- Gitelman's syndrome as common cause of hypokalemia and hypomagnesemia2016 | First Faculty of Medicine
- Transient hyperphosphatasemia: a benign laboratory disorder in a boy with Gitelman syndrome2016 | Faculty of Medicine in Hradec Králové
- Genetic Analysis of Gitelman Syndrome Patients from the Czech Republic and Slovakia - Three Novel Mutations Found2006 | First Faculty of Medicine, Faculty of Science
- Gitelman's Syndrome: A Hereditary Disorder Characterized by Hypokalemia and Hypomagnesaemia +12009 | Publication without faculty affiliation
- Sudden cardiac arrest in a child with Gitelman syndrome: a case report and literature review2023 | Second Faculty of Medicine
- Clinical and genetic diagnosis in Gitelman´s syndromePublication without faculty affiliation
- Mutation analysis in patients with gitelman's syndrome2006 | First Faculty of Medicine
- Gitelman´s syndrome2005 | Faculty of Medicine in Hradec Králové
- Gitelman´s syndrome +12005 | Faculty of Medicine in Hradec Králové, Central Library of Charles University
- DNA Analysis of Renal Electrolyte Transporter Genes Among Patients Suffering from Bartter and Gitelman Syndromes - Summary of Mutation Screening2011 | First Faculty of Medicine
- Gitelman syndrome: novel mutation and long-term follow-up2012 | First Faculty of Medicine
- Mutation Screening for patients with Gitelman Syndrom in the Czech Republic. 2 novel mutations foundPublication without faculty affiliation
- Gitelman´s syndrome (a case report)2005 | Faculty of Medicine in Hradec Králové
- Gitelman´s syndrome (a case report)2005 | Faculty of Medicine in Hradec Králové, Central Library of Charles University
- Homozygous missense mutation in SLC 12A3 gene caused Gitelmanś syndrome with chondrocalcinosisPublication without faculty affiliation
- Genetic analysis of SLC12A3 gene of patients with Gitelman syndrom in the Czech RepublicPublication without faculty affiliation
- Current views on the diagnosis and management of hypokalaemia in children2016 | Second Faculty of Medicine
- Bartter syndrome or renal tubular acidosis?2003 | First Faculty of Medicine