- Genetic variants of transferrin in the diagnostics of proteins hypoglycosylation2005 | First Faculty of Medicine
- Genetic variants of transferrin in the diagnostics of proteins hypoglycosylation2005 | Faculty of Medicine in Hradec Králové
- Genetic variants of transferrin in the diagnostics of proteins hypoglycosylation2005 | Faculty of Medicine in Hradec Králové, Central Library of Charles University
- Transferrin D Protein Variants in the Diagnosis of Congenital Disorders of Glycosylation (CDG)2009 | First Faculty of Medicine
- Screening and diagnosis of congenital disorders of glycosylation2007 | Publication without faculty affiliation
- Screening and diagnosis of congenital disorders of glycosylation2007 | First Faculty of Medicine
- Transferrin D Protein Variants in the Diagnosis of Congenital Disorders of Glycosylation (CDG) +12009 | Faculty of Medicine in Hradec Králové
- Our Experience with Diagnostics of Congenital Disorders of Glycosylation2004 | First Faculty of Medicine
- Serum transferrin microheterogeneity in cystis fibrosis2009 | Faculty of Medicine in Hradec Králové, First Faculty of Medicine, Faculty of Physical Education and Sport
- Microheterogeneity of some serum glycoproteins in neurodegenerative diseases2012 | Faculty of Medicine in Hradec Králové
- Genetic variants of transferrin in cystic fibrosis2008 | Second Faculty of Medicine
- Complex metabolic disharmony in PMM2-CDG paves the way to new therapeutic approaches2023 | First Faculty of Medicine
- Aberrant apolipoprotein C-III glycosylation in glycogen storage disease type III and IX2018 | First Faculty of Medicine
- Phosphomannomutase 2 deficiency: clinical, biochemical and molecular analyses in 22 Czech patients2018 | First Faculty of Medicine
- De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonus2022 | First Faculty of Medicine