- OBJECTIFICATION OF CHANGES IN SELECTED GAIT PARAMETERS IN PATIENTS WITH HEREDITARY NEUROPATHY (CMT) USING KINEMATIC ANALYSIS2010 | First Faculty of Medicine, Faculty of Physical Education and Sport
- Charcot-Marie-Tooth Disease (CMT) - clinical, neurophysiological and genetic aspectsPublication without faculty affiliation
- Clinical findings and diagnostic procedures in CMT2000 | First 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
- Hereditary neuropathies in childhood2022 | Second Faculty of Medicine
- Mutations in the LMNA gene do not cause axonal CMT in Czech patients2009 | Second Faculty of Medicine
- GDAP1 mutations in Czech families with early-onset CMT2007 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Novel EGR2 mutation R359Q is associated with CMT type 1 and progressive scoliosis2005 | Second Faculty of Medicine
- Hearing loss as the first feature of late-onset axonal CMT disease due to a novel P0 mutation2004 | Second Faculty of Medicine
- Nová mutace NEFL-genu v české CMT rodině s časným nástupem axonální neuropatiePublication without faculty affiliation
- Paradoxes of neurogenetic programme: Charcoot Marie Tooth Diseases (CMT) - Hereditary motor sensory neuropathy (HMSN)2003 | Second Faculty of Medicine
- Inherited neuropathy-clinical and electrophysiological findings in the family with CMT X linked neuropathy2002 | Second Faculty of Medicine, Central Library of Charles University
- Low-frequency centroid-moment-tensor inversion from superconducting-gravimeter data: The effect of seismic attenuation2014 | Faculty of Mathematics and Physics
- Near-regional CMT and multiple-point source solution of the September 5, 2012, Nicoya, Costa Rica Mw 7.6 (GCMT) earthquake2014 | Faculty of Mathematics and Physics
- Effect of an R69C Mutation in the Myelin Protein Zero Gene on Myelination and Ion Channel Subtypes2006 | Second Faculty of Medicine
- Examination of cardiovascular reactivity in patients with hereditary neuropathy2014 | Second Faculty of Medicine
- Charcot-Marie-Tooth neuropathy due to a novel EGR2 gene mutation with mild phenotype - Usefulness of human mapping chip linkage analysis in a Czech family2012 | First Faculty of Medicine
- Charcot-Marie-Tooth neuropathy due to a novel EGR2 gene mutation with mild phenotype - Usefulness of human mapping chip linkage analysis in a Czech family2012 | Second Faculty of Medicine
- Phenotypic Variability in a Large Czech Family with a Dynamin 2-Associated Charcot-Marie-Tooth Neuropathy2011 | Second Faculty of Medicine
- Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 22018 | 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
- Magnetic resonance brain findings in Charcot-Marie-Tooth disease, type X12009 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Selected items from the Charcot-Marie-Tooth (CMT) Neuropathy Score and secondary clinical outcome measures serve as sensitive clinical markers of disease severity in CMT1A patients2014 | Second Faculty of Medicine
- Stability disturbances in patients with hereditary motor and sensory neuropathyPublication without faculty affiliation
- Low-Frequency Centroid Moment Tensor Inversion of the 2015 Illapel Earthquake from Superconducting-Gravimeter Data2016 | Faculty of Mathematics and Physics
- Biomarkers predict outcome in Charcot-Marie-Tooth disease 1A2017 | Second Faculty of Medicine
- Hereditary Neuropathy2009 | Second Faculty of Medicine
- Possibilities and indications of orthopedic treatment in Charcot-Marie-Tooth disease2008 | Second Faculty of Medicine
- Clinical and in silico evidence for and against pathogenicity of 11 new mutations in the MPZ gene2010 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine