- Variant pathogenicity evaluation in the community-driven Inherited Neuropathy Variant Browser2018 | Second Faculty of Medicine
- Inherited neuropathies - Interdisciplinary diagnosis2007 | Second Faculty of Medicine
- Inherited neuropathy-clinical and electrophysiological findings in the family with CMT X linked neuropathy2002 | Central Library of Charles University, Second Faculty of Medicine
- PFN2 and GAMT as common molecular determinants of axonal Charcot-Marie-Tooth disease2018 | Second Faculty of Medicine
- 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
- Toxic neuropathies2017 | Second Faculty of Medicine
- SIMPLE mutation in demyelinating neuropathy and distribution in sciatic nerve2004 | Second Faculty of Medicine
- Biomarkers predict outcome in Charcot-Marie-Tooth disease 1A2017 | Second Faculty of Medicine
- Clinical practice guideline for the management of paediatric Charcot-Marie-Tooth disease2022 | Second Faculty of Medicine