Publications
- Linkage between A(TA)7TAA and -3279T>G mutation in UGT1A1 is not essential for pathogenesis of Gilbert syndrome2006 | First Faculty of Medicine
- Dual hereditary jaundice: simultaneous occurence of mutations causing Gilbert's and Dubin-Johnson syndrome2005 | First Faculty of Medicine, Third Faculty of Medicine
- Benign recurrent intrahepatic cholestasis associated with a novel mutation in FIC1/ATP8B1 gene case reportPublication without faculty affiliation
- Exome sequencing reveals IFT172 variants in patients with non-syndromic cholestatic liver disease2023 | First Faculty of Medicine, Third Faculty of Medicine, Second Faculty of Medicine, Central Library of Charles University
- Low Frequency of Cancer-Predisposition Gene Mutations in Liver Transplant Candidates with Hepatocellular Carcinoma2023 | First Faculty of Medicine, Faculty of Science, Central Library of Charles University
- Lysosomal nanotoxicity: Impact of nanomedicines on lysosomal function2023 | Faculty of Mathematics and Physics, Central Library of Charles University
- Iron oxide nanoparticles trigger endoplasmic reticulum damage in steatotic hepatic cells2023 | Faculty of Mathematics and Physics, Central Library of Charles University
- Hepatology2022 | First Faculty of Medicine, Third Faculty of Medicine, Second Faculty of Medicine, Faculty of Medicine in Pilsen, Faculty of Medicine in Hradec Králové
- A mutation in the SAA1 promoter causes hereditary amyloid A amyloidosis2022 | First Faculty of Medicine, Third Faculty of Medicine
- Alpha-1 Antitrypsin and Hepatocellular Carcinoma in Liver Cirrhosis: SERPINA1 MZ or MS Genotype Carriage Decreases the Risk2021 | First Faculty of Medicine, Faculty of Physical Education and Sport, Central Library of Charles University
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