Publications
- PAR1 deletion/duplication in patients with dyschondrosteosis or idiopathic short staturePublication without faculty affiliation
- Complex genetic analysis of SHOX gene in patients with dyschondrosteosis or idiopathic short staturePublication without faculty affiliation
- SHOX gene polymorphic variants and their association with isolated short staturePublication 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
- Mutational screening of inverted formin 2 in adult-onset focal segmental glomerulosclerosis or minimal change patients from the Czech Republic2018 | First Faculty of Medicine
- Molecular Oncology in Case Reports2017 | First Faculty of Medicine, Third Faculty of Medicine
Loading network view...