Publications
- miRNAs and isomiRs: Serum-Based Biomarkers for the Development of Intellectual Disability and Autism Spectrum Disorder in Tuberous Sclerosis Complex2022 | Second Faculty of Medicine
- Pediatric neurology2021 | First Faculty of Medicine, Second Faculty of Medicine
- Monozygotic twins with Legius syndrome and differential diagnosis of Legius syndrome and neurof bromatosis type 12021 | Second Faculty of Medicine
- Torcular dural sinus malformations: a single-center case series and a review of literature2020 | Second Faculty of Medicine
- Jugular Bulb Dysmaturation in Torcular Dural Sinus Malformation: Clinical Images and Review of Literature2019 | Second Faculty of Medicine
- Neurofibromatosis von Recklinghausen type 1 (NF1) - the most common neurocutaneous disorder2018 | Second Faculty of Medicine
- Genotype/phenotype correlation in Czech tuberous sclerosis patients2016 | Second Faculty of Medicine
- 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
- Chromosome 12q13.13 deletions involving the HOXC gene cluster: Phenotype and candidate genes2013 | Second Faculty of Medicine
- Mid-aortic syndrome with renovascular hypertension and multisystem involvement in a girl with familiar neurofibromatosis von Recklinghausen type 12007 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
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