Publikace
- Genetic Testing for Malformations of Cortical Development2022 | 2. lékařská fakulta
- Biallelic variants in the SORD gene are one of the most common causes of hereditary neuropathy among Czech patients2021 | 2. lékařská fakulta
- Severe neurodevelopmental disorder with intractable seizures due to a novel SLC1A4 homozygous variant2021 | 2. lékařská fakulta
- Whole-Exome Sequencing in Czech Patients with Neurogenetic Diseases2020 | 2. lékařská fakulta
- UBTF Mutation Causes Complex Phenotype of Neurodegeneration and Severe Epilepsy in Childhood2019 | 2. lékařská fakulta
- Schinzel-Giedion Syndrome: First Czech Patients Confirmed by Molecular Genetic Analysis2019 | 2. lékařská fakulta
- A 5-year-old boy with super-refractory status epilepticus and RANBP2 variant warranting life-saving hemispherotomy2024 | 2. lékařská fakulta, Ústřední knihovna
- BRAT1 links Integrator and defective RNA processing with neurodegeneration2022 | Přírodovědecká fakulta, Ústřední knihovna
- Retinitis pigmentosa-linked mutation in DHX38 modulates its splicing activity2022 | Přírodovědecká fakulta, Ústřední knihovna
- GATOR1-related focal cortical dysplasia in epilepsy surgery patients and their families: A possible gradient in severity?2021 | 2. lékařská fakulta
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