- Rehabilitation of patients with Charcot-Marie-Tooth disease2003 | Second Faculty of Medicine
- Possibilities of rehabilitation in patients with Charcot-Marie-Tooth disease2002 | Second Faculty of Medicine
- Evaluation of muscle strength and manual dexterity in patients with Charcot-Marie-Tooth disease2016 | Second Faculty of Medicine
- Effect of functional stabilization training on balance and motor patterns in a patient with Charcot-Marie-Tooth disease2012 | Second Faculty of Medicine
- Confirmation of the GNB4 gene as causal for Charcot-Marie-Tooth disease by a novel de novo mutation in a Czech patient2017 | Second Faculty of Medicine
- X-linked Charcot-Marie-Tooth disease: Phenotypic expression of a novel mutation IIe127Ser in the GJB1 (connexin 32) gene2005 | Second Faculty of Medicine
- Charcot-Marie-Tooth Disease (CMT) - clinical, neurophysiological and genetic aspectsPublication without faculty affiliation
- Possibilities and indications of orthopedic treatment in Charcot-Marie-Tooth disease2008 | Second Faculty of Medicine
- Magnetic resonance brain findings in Charcot-Marie-Tooth disease, type X12009 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- 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
- Hereditary Neuropathy2010 | Second Faculty of Medicine
- PFN2 and GAMT as common molecular determinants of axonal Charcot-Marie-Tooth disease2018 | Second Faculty of Medicine
- Charcot-Marie-Tooth gonosomal dominant type (CMTX1) - First findings of mutations in the gene for connexin 32 in the Czech Republic2000 | Second Faculty of Medicine
- Severe axonal Charcot-Marie-Tooth disease with proximal weakness caused by de novo mutation in the MORC2 gene2016 | Second Faculty of Medicine
- Six New Gap Junction Beta 1 Gene Mutations and Their Phenotypic Expression in Czech Patients with Charcot-Marie-Tooth Disease2010 | Second Faculty of Medicine
- Hereditary motor neuropathies2016 | Second Faculty of Medicine
- Hereditary neuropathy +12015 | Second Faculty of Medicine
- Charcot-Marie-Tooth disease type 1A (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP): Reliable detection of the CMT1A duplication and HNPP deletion using 8 microsatellite markers in 2 multiplex PCRs2000 | Second Faculty of Medicine
- Morbus Charcot-Marie-Tooth - options for orthopedic treatment of deformities of the foot2015 | 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
- A 71-nucleotide deletion in the periaxin gene in a Romani patient with early-onset slowly progressive demyelinating CMT2008 | Second Faculty of Medicine
- Charcot-Marie-Tooth neuropathy type 1A combined with Duchenne muscular dystrophy2007 | Second Faculty of Medicine
- Pes Cavus2015 | Faculty of Medicine in Pilsen
- Novel EGR2 mutation R359Q is associated with CMT type 1 and progressive scoliosis2005 | Second Faculty of Medicine
- GDAP1 mutations in Czech families with early-onset CMT2007 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Characterization of molecular mechanisms underlying the axonal Charcot-Marie-Tooth neuropathy caused by MORC2 mutations2019 | Second Faculty of Medicine
- Pulmonary function in patients with hereditary motor and sensory neuropathy: A comparison of patients with and without spinal deformity2012 | Second Faculty of Medicine
- Pulmonary function in patients with hereditary motor and sensory neuropathy: A comparison of patients with and without spinal deformity2012 | First Faculty of Medicine