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
- Alteration of the Circadian Clock in Children with Smith-Magenis Syndrome2012 | First Faculty of Medicine
- Polysomnographic Findings in Children with Attention-Deficit/Hyperactivity Disorder Investigated for Sleep2012 | First Faculty of Medicine
- Motor Stereotypies in Childhood - Case Reports2012 | First Faculty of Medicine
- Sleep Microstructure Is Not Altered in Children With Attention-Deficit/Hyperactivity Disorder (ADHD)2012 | 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
- Spinal Complications in Genetic Syndromes - Case Reports2011 | First Faculty of Medicine
- Diagnosing narcolepsy with cataplexy on history alone: challenging the International Classification of Sleep Disorders (ICSD-2) criteria2011 | First Faculty of Medicine
- Genetic disorders and sleepiness: medical, psychiatric and neurological causes of sleepiness2011 | First Faculty of Medicine
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