- Shprintzen-Goldbergův syndrom2018 | Second Faculty of Medicine
- Girl with congenital disorder of glycosylation - case report2009 | First Faculty of Medicine
- Girl with congenital disorder of glycosylation - case report2009 | Publication without faculty affiliation
- Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation2010 | First Faculty of Medicine
- Laterality in children: cerebellar dominance, handedness, footedness and hair whorl2009 | First Faculty of Medicine
- Congenital hypomyelination in conjunction with de-novo mutation in the gene for the peripheral myelin protein 22 - the first confirmed case in the CR and review of the literature2002 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Application of neurophysiological procedures in neurogenic pareses of abdominal wall2011 | Second Faculty of Medicine
- Congenital muscular dystrophy with complete defect of merosine - First two cases confirmed in the Czech Republic - Typical phenotype and evidence based on skin biopsy2002 | Second Faculty of Medicine