- Possibilities and indications of orthopedic treatment in Charcot-Marie-Tooth disease2008 | Second Faculty of Medicine
- Possibilities of rehabilitation in patients with Charcot-Marie-Tooth disease2002 | Second Faculty of Medicine
- Morbus Charcot-Marie-Tooth - options for orthopedic treatment of deformities of the foot2015 | Second Faculty of Medicine
- Morbus Charcot-Marie-Tooth - Case report, Orthopaedic Therapy2003 | Second Faculty of Medicine
- Charcot-Marie-Tooth Disease (CMT) - clinical, neurophysiological and genetic aspectsPublication without faculty affiliation
- Magnetic resonance brain findings in Charcot-Marie-Tooth disease, type X12009 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- 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
- 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
- Charcot-Marie-Tooth 1 (CMT1) and tomaculous neuropathy (HNPP) - Evidence of specific DNA duplications and deletions in the area of 17p11.2-12 by means of a set of dinucleotide markers1999 | Second Faculty of Medicine
- Rehabilitation of patients with Charcot-Marie-Tooth disease2003 | Second Faculty of Medicine
- Hereditary Neuropathy2010 | Second Faculty of Medicine
- Pes Cavus2015 | Faculty of Medicine in Pilsen
- Utility of Charcot-Marie-Tooth Neuropathy Score in Children With Type 1A Disease2010 | Second Faculty of Medicine
- Charcot-Marie-Tooth type X : A novel mutation in the Cx32 gene with central conduction slowing2001 | Second Faculty of Medicine
- Demyelinating Charcot Marie Tooth neuropathy associated with FBLN5 mutations2020 | Second Faculty of Medicine
- Clinical practice guideline for the management of paediatric Charcot-Marie-Tooth disease2022 | Second Faculty of Medicine
- Charcot-Marie-Tooth neuropathy type 1A combined with Duchenne muscular dystrophy2007 | Second Faculty of Medicine
- Hereditary neuropathy +12015 | Second Faculty of Medicine
- Lower urinary tract functions in a series of Charcot-Marie-Tooth neuropathy patients2014 | 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
- Novel SBF2 mutations and clinical spectrum of Charcot-Marie-Tooth neuropathy type 4B22018 | Second Faculty of Medicine
- MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 22006 | Second Faculty of Medicine
- Hereditary motor neuropathies2016 | Second Faculty of Medicine
- Charcot-Marie-Tooth 1A: heterozygous T118M mutation over a CMT1A duplication has no influence on the phenotype1999 | Second Faculty of Medicine
- Evaluation of muscle strength and manual dexterity in patients with Charcot-Marie-Tooth disease2016 | Second Faculty of Medicine
- Back pain in hereditary neuropathy2002 | 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
- Examination of cardiovascular reactivity in patients with hereditary neuropathy2014 | Second Faculty of Medicine
- Characterization of molecular mechanisms underlying the axonal Charcot-Marie-Tooth neuropathy caused by MORC2 mutations2019 | Second Faculty of Medicine
