Publications
- Detection rate of causal variants in severe childhood epilepsy is highest in patients with seizure onset within the first four weeks of life2018 | Second Faculty of Medicine
- STRC Gene Mutations, Mainly Large Deletions, are a Very Important Cause of Early-Onset Hereditary Hearing Loss in the Czech Population2018 | Second Faculty of Medicine
- HMSN Lom in 12 Czech patients, with one unusual case due to uniparental isodisomy of chromosome 82017 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Two Novel Variants Affecting CDKL5 Transcript Associated with Epileptic Encephalopathy2017 | Second Faculty of Medicine
- Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptom2015 | Second Faculty of Medicine
- Re: 'the effect of antibiotic therapy for Clostridioides difficile infection on mortality and other patient-relevant outcomes' by Stabholz et al2024 | Second Faculty of Medicine
- Update on Microbiota-derived therapies for recurrent Clostridioides difficile infections, 20232024 | Second Faculty of Medicine
- Heterogeneity in practices to reduce the risk of transmission of Clostridioides difficile in healthcare settings: a survey of ESCMID Study Group for Clostridioides difficile (ESGCD) members2024 | Second Faculty of Medicine
- Hospital and community wastewater as a source of multidrug-resistant ESBL-producing Escherichia coli2023 | Second Faculty of Medicine, Faculty of Medicine in Pilsen
- To screen or not to screen medical students for carriage of multidrug-resistant pathogens?2023 | Second Faculty of Medicine, Faculty of Science
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