Study programme
Classes
Publications
- Homozygous EXOSC3 Mutation c.92G -> C, p.G31A is a Founder Mutation Causing Severe Pontocerebellar Hypoplasia Type 1 Among the Czech Roma2013 | Second Faculty of Medicine
- Good interobserver and intraobserver agreement in the evaluation of the new ILAE classification of focal cortical dysplasias2012 | Second Faculty of Medicine
- Unexpected sudden death caused by medullary brain lesions involves all age groups and may include 'sudden infant death syndrome' as a subset2005 | Second Faculty of Medicine, Third Faculty of Medicine
- Microscopic Disorders of Cortical Development of Brain and the Etiopathogenetic Relevance of their Detection in Patients with Temporal Lobe Epilepsy due to Hippocampal Sclerosis2003 | Second Faculty of Medicine
- Advances in the diagnosis of pediatric epilepsy surgery candidates2003 | Second Faculty of Medicine
- Neuropathological findings in patients with mesiotemporal epilepsy: Frequent occurrence of dual pathology2003 | Second Faculty of Medicine
- A 5-year-old boy with super-refractory status epilepticus and RANBP2 variant warranting life-saving hemispherotomy2024 | Second Faculty of Medicine, Central Library of Charles University
- Unusual fusion gene rearrangements in patients with nodular fasciitis: a study of rare and novel USP6 fusion partners with a review of the literature2024 | Second Faculty of Medicine
- Clinical and molecular study of radiation-induced gliomas2024 | Second Faculty of Medicine
- Klinická onkologie2023 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Medicine in Pilsen, Third Faculty of Medicine
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