- Effect of hyperammonemia on leucine and protein metabolism in rats2000 | Faculty of Medicine in Hradec Králové
- Urea cycle disorders, Arginine Chloride in the treatment of hyperammonemia2021 | Publication without faculty affiliation
- Effect of hyperammonemia on leucine and protein metabolism in rats +1Publication without faculty affiliation
- Acute hyperammonemia activates branched-chain amino acid catabolism and decreases their extracellular concentrations: different sensitivity of red and white muscle2011 | Faculty of Medicine in Hradec Králové
- Muscle Amino Acid and Adenine Nucleotide Metabolism during Exercise and in Liver Cirrhosis: Speculations on How to Reduce the Harmful Effects of Ammonia2022 | Faculty of Medicine in Hradec Králové
- Late onset of inherited urea cycle disorder - ornithine transcarbamoylase deficiency2016 | First Faculty of Medicine
- Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation2010 | First Faculty of Medicine
- Comprehensive characterization of ureagenesis in the spf(ash) mouse, a model of human ornithine transcarbamylase deficiency, reveals age-dependency of ammonia detoxification2019 | First Faculty of Medicine
- Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia2014 | First Faculty of Medicine
- Hyperammonemic crisis in a child with ATP synthase deficiency caused by mtDNA mutation m.8851T>C2015 | First Faculty of Medicine
- Valproic acid-induced hyperammonemic encephalopathy in a full-term neonate: a brief review and case report2017 | First Faculty of Medicine
- Neonatal onset of mitochondrial disorders in 129 patients: clinical and laboratory characteristics and a new approach to diagnosis2012 | First Faculty of Medicine
- Evidence of a vicious cycle in glutamine synthesis and breakdown in pathogenesis of hepatic encephalopathy-thereapeutic perspectives2014 | Faculty of Medicine in Hradec Králové
- Branched-Chain Amino Acids and Branched-Chain Keto Acids in Hyperammonemic States: Metabolism and as Supplements2020 | Faculty of Medicine in Hradec Králové
- Characteristic clinical features and laboratory findings of inborn errors of metabolism2018 | First Faculty of Medicine
- Hereditary hyperferritinemia-cataract syndrome in three Czech families: molecular genetic testing and clinical implications2020 | First Faculty of Medicine, Second Faculty of Medicine
- Variable X-chromosome inactivation and enlargement of pericentral glutamine synthetase zones in the liver of heterozygous females with OTC deficiency2018 | First Faculty of Medicine, Central Library of Charles University
- The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation2015 | First Faculty of Medicine