- Atypical course of Gaucher disease2021 | First Faculty of Medicine
- Gaucher disease - current possibilities of therapy2019 | First Faculty of Medicine
- Enzyme replacement therapy for Gaucher disease in twin pregnancy2009 | First Faculty of Medicine
- Gaucher disease2003 | First Faculty of Medicine
- Gaucher disease and lysosomal disorders - current options in evaluation and therapy2016 | First Faculty of Medicine
- Oculomotor and Vestibular Findings in Gaucher Disease Type 3 and Their correlation with Neurological Findings2018 | First Faculty of Medicine
- Enzyme replacement therapy in patients with Gaucher diseasePublication without faculty affiliation
- Genetic and clinical features of patients with Gaucher disease in Hungary2007 | First Faculty of Medicine
- Genetic and clinical features of patients with Gaucher disease in Hungary2007 | Faculty of Physical Education and Sport
- Sustained therapeutic effects of oral miglustat in type I Gaucher disease2004 | First Faculty of Medicine
- Sustained therapeutic effects of oral miglustat in type I Gaucher disease2004 | Faculty of Physical Education and Sport
- Force Majeure: Therapeutic measures in response to restricted supply of imiglucerase (Cerezyme) for patients with Gaucher disease2010 | First Faculty of Medicine
- Enzyme replacement therapy in patients with Gaucher disease in the Czech RepublicPublication without faculty affiliation
- ERT and Gravidity in Gaucher DiseasePublication without faculty affiliation
- 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
- Lysosomal Storage Disorders - Substrat Reduction Therapy in Niemann Pick C and Gaucher DiseasePublication without faculty affiliation
- Future Directions in Gaucher Disease a NPCPublication without faculty affiliation
- Clinical benefits of miglustat on bone disease in adult type 1 Gaucher disease (GD1): A meta-analysisPublication without faculty affiliation
- Abnormal nonstoring capillary endothelium: a novel feature of Gaucher disease. Ultrastructural study of dermal capillaries2010 | First Faculty of Medicine
- Non-skeletal manifestations, complications and management challenges in Gaucher DiseasePublication without faculty affiliation
- Enzyme therapy in children with serve forms of Gaucher's Disease1997 | Faculty of Physical Education and Sport
- Autopsy case of Gaucher disease type I in a patient on enzyme replacement therapy. Comments on the dynamics of persistent storage process +12009 | 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 | Publication without faculty affiliation
- Adenylosukcinatlyasa a její isoforma v lidských tkáníchPublication without faculty affiliation
- 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
- Long-Term Evaluation of Biomarkers in the Czech Cohort of Gaucher Patients2023 | First Faculty of Medicine
- Musculoskeletal involvement in patients with lysosomal storage disease2019 | First Faculty of Medicine
- Glucocerebrosidase gene has an alternative upstream promoter, which has features and expression characteristic of housekeeping genes2011 | First Faculty of Medicine