Publications
- 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
- Hereditary ataxias in the Czech Republic1998 | Second Faculty of Medicine, Central Library of Charles University
- Genotype/phenotype correlations in neuromuscular disorders1998 | Second Faculty of Medicine
- DNA diagnostics of Friedrich's ataxia1997 | Second Faculty of Medicine
- Longitudinal and multidisciplinar care about the patients and families suffering from proximal muscular dystrophyPublication without faculty affiliation
- Correlation neurophysiological and molecular genetic findings in SCA patientsPublication without faculty affiliation
- Poruchy rovnováhy v dětském věku2023 | First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Hemihypoglossal-facial nerve anastomosis: results and electromyographic characterization2022 | First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine
- Outcomes of facial nerve reconstructive surgery2022 | First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine
- The PURPLE N study: objective and perceived nutritional status in children and adolescents with cerebral palsy2022 | Second Faculty of Medicine
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