Publications
- Clinical symptoms and laboratory data in 75 children with neonatal manifestation of mitochondrial disease: Proposed diagnostics algorithms2010 | First Faculty of Medicine
- A new case of ALG8 deficiency (CDG Ih)2009 | First Faculty of Medicine, Third Faculty of Medicine
- Loss of function of Sco1 and its interaction with cytochrome c oxidase2009 | First Faculty of Medicine
- Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF12005 | First Faculty of Medicine
- Blue native polyacrylamide gel electrophoresis to study defects of human cytochrome c oxidase assemblyPublication without faculty affiliation
- Molecular characterization of a novel His333Arg variant of human protoporphyrinogen oxidase IX2022 | First Faculty of Medicine
- Iron Complexes of Flavonoids-Antioxidant Capacity and Beyond2021 | First Faculty of Medicine
- Activity of phosphomannomutase 2 in patients with suspected congenital disorder of glycosylation2016 | First Faculty of Medicine
- High-resolution melting analysis for identifying sequence variations in nuclear genes for assembly factors and structural subunits of cytochrome c oxidase2015 | First Faculty of Medicine
- Large copy number variations in combination with point mutations in the TYMP and SCO2 genes found in two patients with mitochondrial disorders2014 | First Faculty of Medicine
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