- ENT Manifestation of Mucopolysaccharidoses2018 | First Faculty of Medicine
- Enzyme replacement therapy in patients with mucopolysaccharidoses2016 | First Faculty of Medicine
- Mucopolysaccharidoses - clinical manifestations, diagnostics and therapy2013 | First Faculty of Medicine
- Adenotonsillar pathology in mucopolysaccharidoses - lysosomal storage predominates in paracortical CD63+ cells2024 | First Faculty of Medicine, Second Faculty of Medicine
- Placenta analysis of prenatally diagnosed patients reveals early GAG storage in mucopolysaccharidoses II and VI2011 | First Faculty of Medicine
- The birth prevalence of lysosomal storage disorders in the Czech Republic: comparison with data in different populations2010 | First Faculty of Medicine
- Musculoskeletal involvement in patients with lysosomal storage disease2019 | First Faculty of Medicine
- The landscape of Mucopolysaccharidosis in Southern and Eastern European countries: a survey from 19 specialistic centers2022 | First Faculty of Medicine
- Inherited disorders of carbohydrate metabolism2023 | First Faculty of Medicine
- Outcomes of hematopoietic stem cell transplantation for Hurler's syndrome in Europe: a risk factor analysis for graft failure2007 | Second Faculty of Medicine
- Lysosomal storage diseases: current diagnostic and therapeutic options2013 | First Faculty of Medicine
- Disorders of carbohydrate metabolism2012 | First Faculty of Medicine
- Effect of rapid cessation of enzyme replacement therapy: A report of 5 more cases2014 | First Faculty of Medicine
- Stomatological Problems in Child with the II Type Mucopolysaccharidosis2013 | Faculty of Medicine in Pilsen
- Lactosylceramide in lysosomal storage disorders. A comparative immunohistochemical and biochemical study2005 | First Faculty of Medicine
- Enzyme replacement therapy in lysosomal storage diseases2015 | First Faculty of Medicine, Faculty of Physical Education and Sport
- Large Proteoglycan Complexes and Disturbed Collagen Architecture in the Corneal Extracellular Matrix of Mucopolysaccharidosis Type VII (Sly Syndrome)2011 | First Faculty of Medicine
- Otorhinolaryngological manifestations in 61 patients with mucopolysaccharidosis2020 | First Faculty of Medicine, Second Faculty of Medicine