Publications
- Gaucher disease and lysosomal disorders - current options in evaluation and therapy2016 | First Faculty of Medicine
- Atypický průběh Gaucherovy choroby2016 | First Faculty of Medicine
- Enzyme replacement therapy in lysosomal storage diseases2015 | First Faculty of Medicine, Faculty of Physical Education and Sport
- Effect of rapid cessation of enzyme replacement therapy: A report of 5 more cases2014 | First Faculty of Medicine
- Attenuated osteoarticular phenotype of type VI mucopolysaccharidosis: a report of four patients and a review of the literature2014 | First Faculty of Medicine
- Sebelipase alfa over 52 weeks reduces serum transaminases, liver volume and improves serum lipids in patients with lysosomal acid lipase deficiency2014 | First Faculty of Medicine
- Clinical Effect and Safety Profile of Recombinant Human Lysosomal Acid Lipase in Patients With Cholesteryl Ester Storage Disease2013 | First Faculty of Medicine
- Enzymes for therapy of inherited metabolic disorders2012 | First Faculty of Medicine
- Mucopolysaccharidosis I – clinical manifestations in 24 children from the Czech Republic and Slovakia2011 | First Faculty of Medicine
- Autopsy case of Gaucher disease type I in a patient on enzyme replacement therapy. Comments on the dynamics of persistent storage process2009 | First Faculty of Medicine
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