Publikace
- Pseudodominant Nanophthalmos in a Roma Family Caused by a Novel PRSS56 Variant2020 | 1. lékařská fakulta, 2. lékařská fakulta
- Eye movement abnormalities are associated with brainstem atrophy in Wilson disease2020 | 1. lékařská fakulta
- Monogenic variants in dystonia: an exome-wide sequencing study2020 | 1. lékařská fakulta
- Segregation of a novel p.(Ser270Tyr) MAF mutation and p.(Tyr56*) CRYGD variant in a family with dominantly inherited congenital cataracts2017 | 1. lékařská fakulta
- Novel OPA1 missense mutation in a family with optic atrophy and severe widespread neurological disorder2013 | 1. lékařská fakulta
- Žádná asociace s ETM2 lokusem u českých pacientů s familiárním esenciálním tremorem2010 | 1. lékařská fakulta
- Caudate nucleus atrophy in Huntington's disease and its relationship with clinical and genetic parameters2005 | 1. lékařská fakulta
- Caudate nucleus atrophy in Huntington's disease and its relationship with clinical and genetic parameters2005 | Fakulta tělesné výchovy a sportu
- Is retina affected in Huntington's disease? Is optical coherence tomography a good biomarker?2023 | 1. lékařská fakulta
- Essential and dystonic head tremor: More similarities than differences2023 | 1. lékařská fakulta
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