Publications
- Charcot-Marie-Tooth neuropathy due to a novel EGR2 gene mutation with mild phenotype - Usefulness of human mapping chip linkage analysis in a Czech family2012 | First Faculty of Medicine
- 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
- Genetic disorders and sleepiness: medical, psychiatric and neurological causes of sleepiness2011 | First Faculty of Medicine
- Sleep disorders in Wilson's disease2011 | First Faculty of Medicine
- Olfactory dysfunction in narcolepsy with and without cataplexy2010 | First Faculty of Medicine
- Narcolepsy in children +12010 | First Faculty of Medicine
- Neurogenetic and metabolic disorders in childhood2010 | First Faculty of Medicine
- Wilson's disease +12009 | First Faculty of Medicine
- Narcolepsy in childhood2009 | First Faculty of Medicine
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