- Poruchy cyklu močoviny, Arginin Chlorid v léčbě hyperamonémie2021 | Publikace bez příslušnosti k fakultě
- Pozdní manifestace dědičné poruchy cyklu močoviny - deficit ornitintranskarbamoylázy2016 | 1. lékařská fakulta
- Dědičné poruchy metabolismu aminokyselin, organických kyselin a cyklu močoviny2022 | 1. lékařská fakulta
- Transatlantic combined and comparative data analysis of 1095 patients with urea cycle disordersA successful strategy for clinical research of rare diseasesPublikace bez příslušnosti k fakultě
- The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation2015 | 1. lékařská fakulta
- The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype2015 | 1. lékařská fakulta
- Proteomic analysis of hepatic iron overload in mice suggests dysregulation of urea cycle, impairment of fatty acid oxidation, and changes in the methylation cycle2007 | 1. lékařská fakulta
- Proteomic analysis of hepatic iron overload in mice suggests dysregulation of urea cycle, impairment of fatty acid oxidation, and changes in the methylation cycle2007 | Fakulta tělesné výchovy a sportu
- Behavioural and emotional problems, intellectual impairment and health-related quality of life in patients with organic acidurias and urea cycle disorders2016 | 1. lékařská fakulta
- Age at disease onset and peak ammonium level rather than interventional variables predict the neurological outcome in urea cycle disorders2016 | 1. lékařská fakulta
- Aspartate-glutamate carrier 2 (citrin): a role in glucose and amino acid metabolism in the liver2023 | Lékařská fakulta v Hradci Králové
- Roles of malate and aspartate in gluconeogenesis in various physiological and pathological states2023 | Lékařská fakulta v Hradci Králové
- Branched-Chain Amino Acids and Branched-Chain Keto Acids in Hyperammonemic States: Metabolism and as Supplements2020 | Lékařská fakulta v Hradci Králové
- Ornithine carbamoyltransferase deficiency: molecular characterization of 29 families2013 | 1. lékařská fakulta
- Activity of the liver enzyme ornithine carbamoyltransferase (OTC) in blood: LC-MS/MS assay for non-invasive diagnosis of ornithine carbamoyltransferase deficiency2017 | 1. lékařská fakulta
- Comprehensive characterization of ureagenesis in the spf(ash) mouse, a model of human ornithine transcarbamylase deficiency, reveals age-dependency of ammonia detoxification2019 | 1. lékařská fakulta
- Aspartic acid in health and disease2023 | Lékařská fakulta v Hradci Králové
- New polymorphic sites within ornithine transcarbamylase gene: population genetics and implications for diagnosis2003 | 1. lékařská fakulta
- Impact of creatine on coordination of urea and citrate cycles2006 | 1. lékařská fakulta
- New polymorphic sites within ornithine transcarbamylase gene: population genetics and implications for diagnosis2003 | Fakulta tělesné výchovy a sportu
- Psychiatrická manifestace dědičných metabolických poruch2015 | 1. lékařská fakulta, Fakulta tělesné výchovy a sportu
- Hydrogenosome-localization of arginine deiminase in Trichomonas vaginalis2011 | Přírodovědecká fakulta
- Phenylbutyrate exerts adverse effects on liver regeneration and amino acid concentrations in partially hepatectomized rats2016 | Lékařská fakulta v Hradci Králové
- Thermoneutral housing promotes hepatic steatosis in standard diet-fed C57BL/6N mice, with a less pronounced effect on NAFLD progression upon high-fat feeding2023 | Přírodovědecká fakulta, Fakulta tělesné výchovy a sportu, Ústřední knihovna
- Arginine deiminase pathway enzymes: evolutionary history in metamonads and other eukaryotes2016 | Přírodovědecká fakulta
- Acute effects of phenylbutyrate on glutamine, branched-chain amino acid and protein metabolism in skeletal muscles of rats2017 | Lékařská fakulta v Hradci Králové
- Branched-chain amino acids in health and disease: metabolism, alterations in blood plasma, and as supplements2018 | Lékařská fakulta v Hradci Králové
