Publikace
- Detection rate of causal variants in severe childhood epilepsy is highest in patients with seizure onset within the first four weeks of life2018 | 2. lékařská fakulta
- Severe axonal Charcot-Marie-Tooth disease with proximal weakness caused by de novo mutation in the MORC2 gene2016 | 2. lékařská fakulta
- COX6A1 mutation causes axonal hereditary motor and sensory neuropathy - the confirmation of the primary report2016 | 2. lékařská fakulta
- Clostridium difficile ribotype 078 cultured from post-surgical non-healing wound in a patient carrying ribotype 014 in the intestinal tract2015 | 2. lékařská fakulta
- Homozygous EXOSC3 Mutation c.92G -> C, p.G31A is a Founder Mutation Causing Severe Pontocerebellar Hypoplasia Type 1 Among the Czech Roma2013 | 2. lékařská fakulta
- Re: 'the effect of antibiotic therapy for Clostridioides difficile infection on mortality and other patient-relevant outcomes' by Stabholz et al2024 | 2. lékařská fakulta
- Update on Microbiota-derived therapies for recurrent Clostridioides difficile infections, 20232024 | 2. lékařská fakulta
- 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 | 2. lékařská fakulta
- Hospital and community wastewater as a source of multidrug-resistant ESBL-producing Escherichia coli2023 | 2. lékařská fakulta, Lékařská fakulta v Plzni
- To screen or not to screen medical students for carriage of multidrug-resistant pathogens?2023 | 2. lékařská fakulta, Přírodovědecká fakulta
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