Publications
- A Novel Frameshift Mutation in the AFG3L2 Gene in a Patient with Spinocerebellar Ataxia2014 | Second Faculty of Medicine
- Spinocerebellar Ataxias Type 8, 12, and 17 and Dentatorubro-Pallidoluysian Atrophy in Czech Ataxic Patients2013 | First Faculty of Medicine, Second Faculty of Medicine, Central Library of Charles University
- Spinocerebellar Ataxia 7 - a Case Report2013 | First Faculty of Medicine, Second Faculty of Medicine
- Uses of the postural stability test for differential diagnosis of hereditary ataxias2012 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Cognitive changes in spinocerebellar ataxia type 22011 | First Faculty of Medicine, Faculty of Physical Education and Sport, Faculty of Medicine in Hradec Králové
- Nonlinear analysis of the sleep EEG in children with pervasive developmental disorder2008 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Prader-Willi syndrome due to uniparental disomy in a patient with a balanced chromosomal translocation2006 | Second Faculty of Medicine
- A series of Czech patients and a survey of current views of biology and differential diagnosis2006 | Second Faculty of Medicine
- Diagnostic possibilities of Prader-Willi and of Angelman syndromes2005 | Second Faculty of Medicine
- EEG abnormalities are not associated with symptom severity in childhood autism2004 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
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