- Enzyme replacement therapy (ERT) in females with Fabry disease: an update from FOS - the Fabry Outcome SurveyPublication without faculty affiliation
- Narrative review on Morbus Fabry: diagnosis and management of cardiac manifestations2021 | First Faculty of Medicine
- Enzyme replacement therapy in patients with mucopolysaccharidoses2016 | First Faculty of Medicine
- Musculoskeletal involvement in patients with lysosomal storage disease2019 | First Faculty of Medicine
- Effect of miglustat on bone disease in adults with type 1 Gaucher disease: A pooled analysis of three multinational, open-label studies +12007 | First Faculty of Medicine
- Effect of miglustat on bone disease in adults with type 1 Gaucher disease: A pooled analysis of three multinational, open-label studies2007 | Publication without faculty affiliation
- Fabry disease and its cardiac involvement2018 | First Faculty of Medicine
- Fabry disease +12018 | First Faculty of Medicine
- Effect of rapid cessation of enzyme replacement therapy: A report of 5 more cases2014 | First Faculty of Medicine
- Early cardiac changes in children with Anderson-Fabry disease2013 | First Faculty of Medicine
- Enzyme replacement therapy for Gaucher disease in twin pregnancy2009 | First Faculty of Medicine
- Enzyme replacement with PEGylated cystathionine beta-synthase ameliorates homocystinuria in murine model2016 | First Faculty of Medicine
- Enzyme Replacement Therapy Ameliorates Multiple Symptoms of Murine Homocystinuria2018 | First Faculty of Medicine
- Long-Term Evaluation of Biomarkers in the Czech Cohort of Gaucher Patients2023 | First Faculty of Medicine
- Fabry disease revisited: Management and treatment recommendations for adult patients2018 | First Faculty of Medicine
- Enzyme replacement therapy in lysosomal storage diseases2015 | First Faculty of Medicine, Faculty of Physical Education and Sport
- The effect of enzyme replacement therapy on clinical outcomes in male patients with Fabry disease: A systematic literature review by a European panel of experts2019 | First Faculty of Medicine
- Mucopolysaccharidosis I - clinical manifestations in 24 children from the Czech Republic and Slovakia2011 | Second 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
- Findings from the Morquio A Registry Study (MARS) after 6 years: Long-term outcomes of MPS IVA patients treated with elosulfase alfa2022 | First Faculty of Medicine