Publikace
- Novel CDKL5 Mutations in Czech Patients with Phenotypes of Atypical Rett Syndrome and Early-Onset Epileptic Encephalopathy2016 | 1. lékařská fakulta, Ústřední knihovna
- Comparison of transcranial sonography-magnetic resonance fusion imaging in Wilson's and early-onset Parkinson's diseases2016 | 1. lékařská fakulta
- MECP2 mutations in Czech patients with Rett syndrome and Rett-like phenotypes: novel mutations, genotype-phenotype correlations and validation of high-resolution melting analysis for mutation scanning2016 | 1. lékařská fakulta
- Parkin (PARK 2) Mutations Are Rare in Czech Patients with Early-Onset Parkinson's Disease2014 | 1. lékařská fakulta
- Wilsonova nemoc2013 | 1. lékařská fakulta
- Rett syndrome2013 | 1. lékařská fakulta
- APOE epsilon4, potenciální modulační faktor Rettova syndromu2010 | 1. lékařská fakulta
- Rettův syndrom2009 | 1. lékařská fakulta
- Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms2007 | 1. lékařská fakulta
- Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms2007 | Fakulta tělesné výchovy a sportu
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