Publikace
- Different laboratory and muscle biopsy findings in a family with an m.8851T > C mutation in the mitochondrial MTATP6 gene2013 | 1. lékařská fakulta, 2. lékařská fakulta
- Neonatal onset of mitochondrial disorders in 129 patients: clinical and laboratory characteristics and a new approach to diagnosis2012 | 1. lékařská fakulta
- Two Patients with Clinically Distinct Manifestation of Pyruvate Dehydrogenase Deficiency Due to Mutations in PDHA1 Gene2011 | 1. lékařská fakulta
- Specific Properties of Heavy Fraction of Mitochondria from Human-term Placenta – Glycerophosphate-dependent Hydrogen Peroxide2006 | 1. lékařská fakulta
- Specific Properties of Heavy Fraction of Mitochondria from Human-term Placenta – Glycerophosphate-dependent Hydrogen Peroxide2006 | Fakulta tělesné výchovy a sportu
- Time-course of hormonal induction of mitochondrial glycerophosphate dehydrogenase biogenesis in rat liver2005 | 1. lékařská fakulta
- Time-course of hormonal induction of mitochondrial glycerophosphate dehydrogenase biogenesis in rat liver2005 | Fakulta tělesné výchovy a sportu
- Pathophysiological role of mitochondrial glycerophosphate dehydrogenasePublikace bez příslušnosti k fakultě
- Familial hypercholesterolaemia in children and adolescents from 48 countries: a cross-sectional study2024 | 1. lékařská fakulta, Lékařská fakulta v Hradci Králové, 2. lékařská fakulta, Lékařská fakulta v Plzni
- Alterations in lipidome profiles distinguish early-onset hyperuricemia, gout, and the effect of urate-lowering treatment2023 | 1. lékařská fakulta, Matematicko-fyzikální fakulta
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