- Modeling new therapies for infantile spasms2010 | Third Faculty of Medicine
- Genetic heterogeneity in infantile spasms2019 | Second Faculty of Medicine
- A model of symptomatic infantile spasms syndrome2010 | Third Faculty of Medicine
- Recessive mutations in SLC35A3 cause early onset epileptic encephalopathy with skeletal defects2017 | Second Faculty of Medicine
- Novel CDKL5 Mutations in Czech Patients with Phenotypes of Atypical Rett Syndrome and Early-Onset Epileptic Encephalopathy2016 | Central Library of Charles University, First Faculty of Medicine
- STXBP1 encephalopathy A neurodevelopmental disorder including epilepsy2016 | Second Faculty of Medicine
- Anti-convulsant agents: Cortisone and Adrenocorticotropic Hormone (ACTH)2022 | Second Faculty of Medicine
- PREDICTORS OF NEUROPSYCHOLOGICAL DYSFUNCTION IN CHILDREN WITH INTRACTABLE EPILEPSY DUE TO TUBEROUS SCLEROSISPublication without faculty affiliation
- Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data2017 | Second Faculty of Medicine
- West syndrome model: seek and you will find1997 | Third Faculty of Medicine
- The landscape of epilepsy-related GATOR1 variants2019 | Second Faculty of Medicine
- De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies2014 | Second Faculty of Medicine
- Predictors of seizure-free outcome after epilepsy surgery for pediatric tuberous sclerosis complex2013 | Second Faculty of Medicine
- Prevention of epilepsy in infants with Tuberous Sclerosis Complex in the EPISTOP trial2021 | Second Faculty of Medicine
- A survey of the European Reference Network EpiCARE on clinical practice for selected rare epilepsies2021 | Second Faculty of Medicine
- Male patient with ALG13 associated congenital disorder of glycosylation2021 | Second Faculty of Medicine