Publications
- CANVAS - a newly identified genetic cause of late-onset ataxia. Description of the first cases in the Czech Republic2021 | First Faculty of Medicine, Second Faculty of Medicine
- The Importance of Posterior Column Signs for Differential Diagnosis of Hereditary Ataxias2013 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Importance of posterior column signs for differential diagnosis of hereditary ataxias2013 | Second Faculty of Medicine, Faculty of Physical Education and Sport
- CLCN1 Mutations in Czech Patients with Myotonia Congenita, In Silico Analysis of Novel and Known Mutations in the Human Dimeric Skeletal Muscle Chloride Channel2013 | Second Faculty of Medicine
- Myotonic dystrophies2012 | Second Faculty of Medicine
- Highly Unstable Sequence Interruptions of the CTG Repeat in the Myotonic Dystrophy Gene2009 | Second Faculty of Medicine
- Fluorescent multiplex PCR: Fast method for autosomal dominant spinocerebellar ataxias screening2005 | Second Faculty of Medicine
- Genotype/phenotype correlations in neuromuscular disorders1998 | Second Faculty of Medicine
- Genotype/phenotype correlations in DMD/BMD and HMSN1998 | Second Faculty of Medicine
- Examining the Correlation Between Neurofilament Levels and Clinical Features in a Friedreich Ataxia Cohort from the Czech Republic2023 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
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