- Hereditary spastic paraplegia 3A associated with axonal neuropathy2007 | Second Faculty of Medicine
- The genetic landscape of axonal neuropathies in the middle-aged and elderly: Focus on MME2020 | Second Faculty of Medicine
- Discrimination of axonal neuropathy using sensitivity and specificity statistical measures2014 | Faculty of Medicine in Hradec Králové
- Extending the clinical spectrum of SPG3A mutations to a very severe and very early complicated phenotype2008 | Second Faculty of Medicine
- Neuropathies due to ethanol abuse2018 | Third Faculty of Medicine
- Spectrum and frequencies of mutations in the MFN2 gene and its phenotypical expression in Czech hereditary motor and sensory neuropathy type II patients2013 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Cranial nerves palsy as an initial feature of an early onset distal hereditary motor neuropathy - A new distal hereditary motor neuropathy phenotype2009 | Second Faculty of Medicine
- Neuromuscular disorders in thyroid disease2012 | Second Faculty of Medicine
- Peripheral neuropathy in Whipple’s disease: A case report2012 | Second Faculty of Medicine
- Severe chronic lithium intoxication in patient treated for bipolar disorder2017 | Third Faculty of Medicine
- Permutation Entropy and Signal Energy Increase the Accuracy of Neuropathic Change Detection in Needle EMG2018 | Faculty of Medicine in Hradec Králové
- Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptom2015 | Second Faculty of Medicine
- Loss of function mutations in HARS cause a spectrum of inherited peripheral neuropathies2015 | Second Faculty of Medicine
- Effect of an R69C Mutation in the Myelin Protein Zero Gene on Myelination and Ion Channel Subtypes2006 | Second Faculty of Medicine
- Divergent phenotypes of Charcot-Marie-Tooth disease: demyelinating with childhood onset and axonal with late onset and slow pupillary reaction, resulting from different myelin protein zero (MPZ, P0) gene mutations2004 | Second Faculty of Medicine