Publications
- Long-term follow-up of Wilson Disease: natural history, treatment, mutations analysis and phenotypic correlation2011 | First Faculty of Medicine, Second Faculty of Medicine
- Mutation analysis of ATP7A and ATP7BPublication without faculty affiliation
- Parkin (PARK 2) Mutations Are Rare in Czech Patients with Early-Onset Parkinson's Disease2014 | First Faculty of Medicine
- Decreased serum antioxidant capacity in patients with Wilson disease is associated with neurological symptoms2012 | 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
- Wilson's disease2009 | First Faculty of Medicine
- Biochemical and molecular analysis in three patients with 3-hydroxy-3-methylglutaric aciduria2003 | First Faculty of Medicine
- Cardiac involvement in Wilson disease2002 | First Faculty of Medicine
- ApoE e4 positive multiple sclerosis patients develop more gray matter and whole brain atrophy: a 4-year longitudinal study using the 15-year disease onset modelPublication without faculty affiliation
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