- Hereditary spastic paraplegias: clinical and genetic aspects2016 | Second Faculty of Medicine
- Augmentation cystoplasty in patients with multiple sclerosis2003 | Third Faculty of Medicine
- Spinal shock - from pathophysiology to clinical manifestation2015 | Second Faculty of Medicine, Third Faculty of Medicine
- Serotonin syndrome: diagnosis, treatment, prophylaxis2001 | Publication without faculty affiliation
- Overactive bladder2005 | Publication without faculty affiliation
- Pelizaeus Merzbacher's disease (PMD) - Detection of the most frequent mutation of the proteolipid protein gene in Czech patients and families with the classical form of PAID2003 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Bickerstaff brainstem encephalitis and Guillain-Barre syndrome overlap2022 | Third Faculty of Medicine, Central Library of Charles University
- Allgrove syndrome with prominent neurological symptoms2016 | Central Library of Charles University
- Megalencephalic leukoencephalopathy with subcortical cysts without macrocephaly: A case study of comorbid Turner's syndrome2019 | Second Faculty of Medicine, First Faculty of Medicine
- A Novel Frameshift Mutation in the AFG3L2 Gene in a Patient with Spinocerebellar Ataxia2014 | Second Faculty of Medicine
- The phenotypic spectrum of SCN8A encephalopathy2015 | Second Faculty of Medicine
- Clinical features and blood iron metabolism markers in children with beta-propeller protein associated neurodegeneration2020 | Second Faculty of Medicine, First Faculty of Medicine
- A severe connatal form of Pelizaeus Merzbacher disease in a Czech boy caused by a novel mutation (725C > A, Ala242Glu) at the 'Jimpy(msd) codon' in the PLP gene2002 | Second Faculty of Medicine