- Deformities of the spine in hereditary motor-sensory neuropathy2005 | 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
- Pulmonary function in patients with hereditary motor and sensory neuropathy: A comparison of patients with and without spinal deformity2012 | Second Faculty of Medicine
- Hereditary motor neuropathies2016 | 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
- 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
- Most important rules of prosthetic care in patients suffering from hereditary motor and sensory neuropathy (HMSN) +12005 | Second Faculty of Medicine
- Stability disturbances in patients with hereditary motor and sensory neuropathyPublication without faculty affiliation
- COX6A1 mutation causes axonal hereditary motor and sensory neuropathy - the confirmation of the primary report2016 | Second Faculty of Medicine
- Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype-phenotype correlation study2008 | Second Faculty of Medicine
- Spinal deformities in hereditary motor and sensory neuropathy - A retrospective qualitative, quantitative, genotypical, and familial analysis of 175 patients2007 | 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
- Paradoxes of neurogenetic programme: Charcoot Marie Tooth Diseases (CMT) - Hereditary motor sensory neuropathy (HMSN)2003 | Second Faculty of Medicine
- HSMNR belongs to the most frequent types of hereditary neuropathy in the Czech Republic and is twice more frequent than HMSNL2016 | 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
- Pes Cavus2015 | Faculty of Medicine in Pilsen
- HMSN Lom in 12 Czech patients, with one unusual case due to uniparental isodisomy of chromosome 82017 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Loss of function mutations in HARS cause a spectrum of inherited peripheral neuropathies2015 | Second Faculty of Medicine
- Morbus Charcot-Marie-Tooth - options for orthopedic treatment of deformities of the foot2015 | Second Faculty of Medicine
- Examination of cardiovascular reactivity in patients with hereditary neuropathy2014 | Second Faculty of Medicine
- Evaluation of muscle strength and manual dexterity in patients with Charcot-Marie-Tooth disease2016 | 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 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
- Mutations in the LMNA gene do not cause axonal CMT in Czech patients2009 | Second Faculty of Medicine
- Hereditary neuropathiesPublication without faculty affiliation
- Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy2004 | Second Faculty of Medicine
- Peripheral neuropathy in children2018 | 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
- Rehabilitation of polyneuropathic syndromes2006 | Second Faculty of Medicine