Publications
- Autosomal dominant polycystic kidney disease in a family with mosaicism and hypomorphic allele2013 | First Faculty of Medicine
- TRPC6 gene variants in Czech adult patients with focal segmental glomerulosclerosis and minimal change disease2012 | 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
- New mutations in the PKD1 gene in Czech population with autosomal dominant polycystic kidney disease2009 | First Faculty of Medicine
- The Correlation of Genotype and Phenotype in Children with Autosomal Dominant Polycystic Kidney DiseasePublication without faculty affiliation
- Ambulatory blood pressure and hypertension control in children with autosomal recessive polycystic kidney disease: clinical experience from two central European tertiary centres2022 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Improvement of Diagnostic Yield by an Additional Amplicon Module to Hybridization-Based Next-Generation Sequencing Panels2022 | First Faculty of Medicine
- Results of targeted next-generation sequencing in children with cystic kidney diseases often change the clinical diagnosis2020 | First Faculty of Medicine, Second Faculty of Medicine
- Two Czech patients with familial adenomatous polyposis presenting mosaicism in APC gene2019 | First Faculty of Medicine
- Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease - a case report2018 | First Faculty of Medicine
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