Publications
- Amniotic fluid alpha-fetoprotein microheterogeneity in the prenatal diagnosis of congenital disorders of glycosylation type Ia2010 | Faculty of Medicine in Hradec Králové
- Genetic variants of transferrin in cystic fibrosis +12008 | Faculty of Medicine in Hradec Králové
- Genetic variants of transferrin in cystic fibrosis2008 | First Faculty of Medicine
- Screening and diagnosis of congenital disorders of glycosylation +12007 | Faculty of Medicine in Hradec Králové
- Screening and diagnosis of congenital disorders of glycosylation2007 | Publication without faculty affiliation
- Methodic Guide to Diagnostics of Congenital Disorders of Glycosylation (CDG)2003 | First Faculty of Medicine
- Pitfalls in screening for inborn errors of metabolism (IEM)Publication without faculty affiliation
- Screening methods in the diagnostics of congenital disorders of glycosylation - our experiencesPublication without faculty affiliation
- Screening and diagnostics of congenital disorders of glycosylationPublication without faculty affiliation
- Mortality benefit of primary transportation to a PCI-capable center persists through an eight-year follow-up in patients with ST-segment elevation myocardial infarction2017 | Faculty of Medicine in Hradec Králové
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