Publications
- Oculomotor and Vestibular Findings in Gaucher Disease Type 3 and Their correlation with Neurological Findings2018 | First Faculty of Medicine
- Enzyme replacement therapy in lysosomal storage diseases2015 | First Faculty of Medicine, Faculty of Physical Education and Sport
- Attenuated osteoarticular phenotype of type VI mucopolysaccharidosis: a report of four patients and a review of the literature2014 | First Faculty of Medicine
- A Prospective Study in Children With a Severe Form of Atopic Dermatitis: Clinical Outcome in Relation to Cytokine Gene Polymorphisms2012 | First Faculty of Medicine
- Long-Term Evaluation of Biomarkers in the Czech Cohort of Gaucher Patients2023 | First Faculty of Medicine
- Lysosomal acid lipase deficiency - differential diagnosis and treatment options in 20222022 | First Faculty of Medicine
- A cross-sectional, prospective ocular motor study in 72 patients with Niemann-Pick disease type C2021 | First Faculty of Medicine
- The late-onset form of Pompe disease2021 | First Faculty of Medicine
- Atypical course of Gaucher disease2021 | First Faculty of Medicine
- Otorhinolaryngological manifestations in 61 patients with mucopolysaccharidosis2020 | First Faculty of Medicine, Second Faculty of Medicine
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