- Girl with congenital disorder of glycosylation - case report2009 | First Faculty of Medicine
- Girl with congenital disorder of glycosylation - case report2009 | Publication without faculty affiliation
- Congenital disorders of glycosylation (CDG Syndrome) in fourteen children with psychomotor delay, hypotonia, strabismus and other various organ involvement +1Publication without faculty affiliation
- An inherited 2q13 deletion in a patient with Marfan syndromePublication without faculty affiliation
- Clinical Manifestations and Results of Laboratory Examinations in Four Patients with Alpha-Mannosidosis2008 | First Faculty of Medicine
- Clinical Manifestations and Results of Laboratory Examinations in Four Patients with Alpha-Mannosidosis2008 | Publication without faculty affiliation
- Recessive null-allele variants in MAG associated with spastic ataxia, nystagmus, neuropathy, and dystonia2020 | First Faculty of Medicine
- A novel heterozygous RIT1 mutation in a patient with Noonan syndrome, leukopenia, and transient myeloproliferation-a review of the literature2016 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Test of Motor Proficiency Second Edition (BOT-2): Compatibility of the Complete and Short Form and Its Usefulness for Middle-Age School Children2019 | First Faculty of Medicine, Faculty of Physical Education and Sport
- Mucopolysaccharidosis I - clinical manifestations in 24 children from the Czech Republic and Slovakia2011 | Second Faculty of Medicine