Publikace
- Genetic Testing for Malformations of Cortical Development2022 | 2. lékařská fakulta
- Bicuspid aortic valve: a pilot candidate gene-based approach in a representative Czech cohor2020 | 2. lékařská fakulta
- Targeted massively parallel sequencing of a representative cohort of Czech patients with various rare aortopathies demonstrates the clinical utility of genetic testing and the need for a multidisciplinary approach to at risk families2018 | 2. lékařská fakulta
- Distribution of CFTR mutations in the Czech population: Positive impact of integrated clinical and laboratory expertise, detection of novel/de novo alleles and relevance for related/derived populations2013 | 1. lékařská fakulta, Fakulta tělesné výchovy a sportu, 2. lékařská fakulta
- Prospective and parallel assessments of cystic fibrosis newborn screening protocols in the Czech Republic: IRT/DNA/IRT versus IRT/PAP and IRT/PAP/DNA2012 | 2. lékařská fakulta, 3. lékařská fakulta, Ústřední knihovna
- Novorozenecký screening cystické fibrózy v České republice: závěry pilotní studie2007 | 2. lékařská fakulta
- NPHP3-Related Disease: A Possible Risk Factor for Developing Encapsulating Peritoneal Sclerosis2024 | 2. lékařská fakulta
- COL4A1 mutation-related disorder presenting as fetal intracranial bleeding, hydrocephalus, and polymicrogyria2023 | 1. lékařská fakulta, 2. lékařská fakulta
- Constitutively active Lyn kinase causes a cutaneous small vessel vasculitis and liver fibrosis syndrome2023 | 2. lékařská fakulta, Ústřední knihovna
- Schimke immunoosseous dysplasia: an ultra-rare disease. a 20-year case series from the tertiary hospital in the Czech Republic2023 | 2. lékařská fakulta
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