- White matter alteration and cerebellar atrophy are hallmarks of brain MRI in alpha-mannosidosis2021 | First Faculty of Medicine
- Phenytoin - An anti-seizure drug: Overview of its chemistry, pharmacology and toxicology2020 | Publication without faculty affiliation
- Phosphomannomutase 2 deficiency: clinical, biochemical and molecular analyses in 22 Czech patients2018 | First Faculty of Medicine
- Pontocerebellar atrophy is the hallmark neuroradiological finding in late-onset Tay-Sachs disease2022 | First Faculty of Medicine
- Autosomal dominant spinocerebellar ataxias: Review2018 | Faculty of Medicine in Pilsen
- Diagnostically Specific Findings in Posturography - Two Case Reports2012 | Second Faculty of Medicine
- Quantitative brain morphometry identifies cerebellar, cortical, and subcortical gray and white matter atrophy in late-onset Tay-Sachs disease2023 | First Faculty of Medicine
- Late-onset Tay-Sachs Disease Can Mimic Spinal Muscular Atrophy Type III - Two Case Reports2013 | First Faculty of Medicine
- NOTCH2NLC CGG Repeats Are Not Expanded and Skin Biopsy Was Negative in an Infantile Patient With Neuronal Intranuclear Inclusion Disease2020 | First Faculty of Medicine, Faculty of Medicine in Pilsen, Third Faculty of Medicine
- Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration2012 | Second Faculty of Medicine
- Digitized Image Analysis of Insula Echogenicity Detected by TCS-MR Fusion Imaging in Wilson's and Early-Onset Parkinson's Diseases2020 | First Faculty of Medicine
- Structural brain abnormalities in childhood autism2001 | Second Faculty of Medicine
- Amyotrophy, cerebellar impairment and psychiatric disease are the main symptoms in a cohort of 14 Czech patients with the late-onset form of Tay-Sachs disease2019 | First Faculty of Medicine, Second Faculty of Medicine
- Homozygous pathogenic variant in BRAT1 associated with nonprogressive cerebellar ataxia2019 | Faculty of Science
- POLR3B-associated leukodystrophy: clinical, neuroimaging and molecular-genetic analyses in four patients: clinical heterogeneity and novel mutations in POLR3B gene2019 | First Faculty of Medicine, Central Library of Charles University
- Consensus Paper: Cerebellum and Ageing2023 | First Faculty of Medicine