Publications
- Congenital Disorders of Glycosylation Type Ia: Clinical, Biochemical and Molecular Analyses in Two Siblings with Cerebellar Hypoplasia2003 | First Faculty of Medicine
- Hemochromatosis (HFE) and transferrin receptor -1 (TFRC1) genes in sporadic porphyria cutanea tarda (sPCT)2002 | First Faculty of Medicine
- Clinical expression of mutations in genes coding for copper transporting ATP7A and ATP7BPublication without faculty affiliation
- Mutation analysis in Czech patients with porphyria variegataPublication without faculty affiliation
- Respiratory chain complexes in 'non-mitochondrial disorders' (2)Publication without faculty affiliation
- Congenital disorders of glycosylation: biochemical and molecular analysesPublication without faculty affiliation
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