- Genetics of hereditary spastic paraplegias2019 | Second Faculty of Medicine
- Hereditary spastic paraplegias: clinical and genetic aspects2016 | Second Faculty of Medicine
- Phantom feelings in paraplegiaPublication without faculty affiliation
- Dominant KPNA3 Mutations Cause Infantile Onset Hereditary Spastic Paraplegia2021 | Second Faculty of Medicine
- Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia2021 | Second Faculty of Medicine
- Autosomal recessive hereditary spastic paraplegia type SPG35 due to a novel variant in the FA2H gene in a Czech patient2019 | Second Faculty of Medicine
- Disease-Causing Variants in the ATL1 Gene Are a Rare Cause of Hereditary Spastic Paraplegia among Czech Patients2017 | Second Faculty of Medicine
- Hereditary spastic paraplegia 3A associated with axonal neuropathy2007 | Second Faculty of Medicine
- Two types of recessive hereditary spastic paraplegia in Roma patients in compound heterozygous state; no ethnically prevalent variant found2020 | Second Faculty of Medicine
- Spinal shock - from pathophysiology to clinical manifestation2015 | Second Faculty of Medicine, Third Faculty of Medicine
- Spinal Cord Injury : Causes, Consequences, Care management2019 | First Faculty of Medicine, Central Library of Charles University, Second Faculty of Medicine, Third Faculty of Medicine
- Paraplegia as an Unusual Manifestation of Aortic Coarctation2001 | Faculty of Medicine in Hradec Králové, Central Library of Charles University
- Functional profile of active tetraplegics and paraplegics - males and females - in dependence on the lesion level2013 | First Faculty of Medicine, Faculty of Physical Education and Sport
- Sir Ludwig Guttmann 's life and work - Hope for people after spinal cord injury2017 | Faculty of Education
- Paraplegia as an unusual manifestation of aortic coarctation in a young manPublication without faculty affiliation
- Anterior pallidal hyperintensity mimicking the eye of the tiger sign in spastic paraplegia type 72024 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- SPAST mutation spectrum and familial occurrence among Czech patients with pure hereditary spastic paraplegia2016 | Second Faculty of Medicine
- Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia2020 | Second Faculty of Medicine
- Extending the clinical spectrum of SPG3A mutations to a very severe and very early complicated phenotype2008 | Second Faculty of Medicine
- Phantom sensations in spinal cord lesions2004 | First Faculty of Medicine
- Recessive null-allele variants in MAG associated with spastic ataxia, nystagmus, neuropathy, and dystonia2020 | First Faculty of Medicine
- An AP4B1 frameshift mutation in siblings with intellectual disability and spastic tetraplegia further delineates the AP-4 deficiency syndrome2015 | Second Faculty of Medicine
- Ischemic Affection of the Spinal Cord as a Result of the Blunt Thoracic Trauma - A Case Report2008 | Faculty of Medicine in Hradec Králové
- Ischemic Affection of the Spinal Cord as a Result of the Blunt Thoracic Trauma - A Case Report2008 | First Faculty of Medicine
- Clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10 methylenetetrahydrofolate reductase (MTHFR) deficiency2016 | First Faculty of Medicine
- Neurological disorders of gait, balance and posture: a sign-based approach2018 | First Faculty of Medicine
- Acute Traumatic Intervertebral Disc Herniation2023 | Faculty of Medicine in Hradec Králové, First Faculty of Medicine, Faculty of Physical Education and Sport
- Successful treatment of erroneous intrathecal actinomycin D administration by ventriculolumbar perfusion and intrathecal instillation of ascorbic acid and corticosteroids1999 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Tremor-spectrum in spinocerebellar ataxia type 32012 | First Faculty of Medicine
- Dominant (Kjer's) optic atrophy associated with mutations in OPA1 gene2020 | First Faculty of Medicine