- Dědičná onemocnění ledvin2006 | First Faculty of Medicine
- Dědičná onemocnění s glomerulárním postižením2006 | First Faculty of Medicine
- Hereditary eye disease:genetic testing and counseling2015 | First Faculty of Medicine
- Preimplantation genetic diagnosis and monogenic inherited eye diseases2016 | First Faculty of Medicine
- Gitelman's Syndrome: A Hereditary Disorder Characterized by Hypokalemia and Hypomagnesaemia2009 | Publication without faculty affiliation
- The genetics of cardiomyopathies2010 | Publication without faculty affiliation
- Classification and genetics of cardiomyopathies2011 | Publication without faculty affiliation
- Genetic etiology of kidney disease - overview and case studies in accordance with massive parallel sequencing2021 | Second Faculty of Medicine
- Is a chance for slowing down progression CKD in Alport syndrom?Commentary on:KI 81,2012,494-5012012 | First Faculty of Medicine
- Fabryho choroba2015 | First Faculty of Medicine
- Diagnostika a příznaky Fabryho choroby2016 | First Faculty of Medicine
- Muir-Torre syndrome - a phenotypic variant of Lynch syndrome2010 | First Faculty of Medicine, Faculty of Medicine in Pilsen, Central Library of Charles University
- Cystic Fibrosis1999 | Central Library of Charles University, Second Faculty of Medicine
- Muir-Torre syndrome - a phenotypic variant of Lynch syndrome2010 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Tolvaptan in patients with autosomal dominant polycystic kidney disease. Commentary on: NEJM 2012,Torres:Tolvaptan in patients with autosomal dominant polycystic kidney disease2012 | First Faculty of Medicine
- Barakatův syndrom2021 | Faculty of Medicine in Hradec Králové, Third Faculty of Medicine
- Cystic Fibrosis1999 | Second Faculty of Medicine
- Hereditary angioedema, still marginalized diagnosis2017 | Second Faculty of Medicine
- Genetika onemocnění ledvin2015 | First Faculty of Medicine
- Salty Children: What Is Life with Cystic Fibrosis Like?2015 | Faculty of Science
- Current treatment options for hereditary angioedema2017 | Second Faculty of Medicine
- Laparoskopické urologické operace u pacientů s von Hippel-Lindau syndromemPublication without faculty affiliation
- Primary ciliary dyskinesia: Part 1. - Pathogenesis and clinical presentation2009 | Second Faculty of Medicine
- Primary ciliary dyskinesia: Part 2. - Diagnostics and therapy2009 | Second Faculty of Medicine
- Role of lomitapide in treatment of severe familial hypercholesterolaemia2020 | Faculty of Medicine in Hradec Králové
- Autozomálně dominantní polycystická choroba ledvin způsobená mutacemi PKD2 - prevalence, klinický průběh, spektrum mutací a prognóza : komentář2017 | First Faculty of Medicine
- Correlation between biochemical findings, structural and enzymatic abnormalities in mutated HMBS identified in six Israeli families with acute intermittent porphyria2009 | First Faculty of Medicine
- What we might expect in hereditary angioedema with C1 inhibitor deficiency treatment?2017 | Second Faculty of Medicine
- Patient with Cowden syndrome caused by mutations in the PTEN gene2014 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- New mutations in the PKD1 gene in Czech population with autosomal dominant polycystic kidney disease2009 | First Faculty of Medicine