- Protein glycosylation disorders, (CDG syndrome): molecular and biochemical charakteristics of family with CDG type IaPublication without faculty affiliation
- Sugar-mediated lattice contacts in crystals of a plant glycoprotein2002 | Faculty of Science
- Carbohydrate synthesis and biosynthesis technologies for cracking of the glycan code: Recent advances2013 | Faculty of Science
- Biochemical properties of three plant nucleases with anticancer potential2011 | First Faculty of Medicine
- Quantification of Fucosylated Hemopexin and Complement Factor H in Plasma of Patients with Liver Disease2014 | Faculty of Science
- GPI-microdomains: a role in signalling via immunoreceptors1999 | Publication without faculty affiliation
- Mutation of Nogo-B Receptor, a Subunit of cis-Prenyltransferase, Causes a Congenital Disorder of Glycosylation2014 | First Faculty of Medicine
- Prediction of Intact N-Glycopeptide Retention Time Windows in Hydrophilic Interaction Liquid Chromatography2022 | Faculty of Science
- International consensus guidelines for phosphoglucomutase 1 deficiency (PGM1-CDG): Diagnosis, follow-up, and management2021 | First Faculty of Medicine
- Microheterogeneity of some serum glycoproteins in neurodegenerative diseases2012 | Faculty of Medicine in Hradec Králové
- De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonus2022 | First Faculty of Medicine
- A new role for dolichol isoform profile in the diagnostics of CDG disorders2020 | First Faculty of Medicine
- Comparison of Different HILIC Stationary Phases in the Separation of Hemopexin and Immunoglobulin G Glycopeptides and Their Isomers2020 | Faculty of Science
- Comparison of human IgG glycopeptides separation using mixed-mode hydrophilic interaction/ion-exchange liquid chromatography and reversed-phase mode2021 | Faculty of Science
- Cobblestone-like brain dysgenesis and altered glycosylation in congenital cutis laxa, Debre type2008 | Second Faculty of Medicine