Publications
- Decreased serum antioxidant capacity in patients with Wilson disease is associated with neurological symptoms2012 | First Faculty of Medicine
- Long-term follow-up of Wilson Disease: natural history, treatment, mutations analysis and phenotypic correlation2011 | First Faculty of Medicine, Second Faculty of Medicine
- Wilson's disease2009 | First Faculty of Medicine
- Mutations in genes coding for ATP7A and ATP7B (causing Mankes and Wilson disease) in Czech RepublicPublication without faculty affiliation
- Clinical expression of mutations in genes coding for copper transporting ATP7A and ATP7BPublication without faculty affiliation
- Mutation analysis of ATP7A and ATP7BPublication without faculty affiliation
- Mutation Screening in the ATP7A and ATP7B Genes in Czech patients with Menkes Disease and Wilson DiseasePublication without faculty affiliation
- Parkin (PARK 2) Mutations Are Rare in Czech Patients with Early-Onset Parkinson's Disease2014 | First Faculty of Medicine
- Parkin mutations and phenotypic features in Czech patients with early-onset Parkinson's disease2010 | First Faculty of Medicine
- Apolipoprotein E epsilon 4-Positive Multiple Sclerosis Patients Develop More Gray-Matter and Whole-Brain Atrophy: a 15-Year Disease History Model Based on a 4-Year Longitudinal Study2010 | First Faculty of Medicine
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