- The importance of DNA analysis of C282Y, H63D and S65C mutations in the HFE gene2012 | Faculty of Medicine in Hradec Králové
- HFE gene mutations in patients with rheumatic diseases2005 | First Faculty of Medicine, Third Faculty of Medicine, Faculty of Physical Education and Sport
- Imfortance of HFE gene mutations in patogenesis of alcoholic steatofibrosis and nonalcoholic steatosis2001 | First Faculty of Medicine
- The prevalence and role of hemochromatosis gene mutations C282Y, H63D, and S65C in patients with systemic rheumatoid disease2007 | First Faculty of Medicine, Third Faculty of Medicine, Faculty of Physical Education and Sport
- Clinical significance of heterozygotic mutations of the HFE gene in chronic hepatitis C2007 | Third Faculty of Medicine
- Iron overload and HFE gene mutations in Czech patients with chronic liver diseases2012 | Third Faculty of Medicine
- Prevalence of heterozygous HFE gene mutation in chronic liver disease2007 | First Faculty of Medicine, Third Faculty of Medicine
- High prevalence of HFE gene mutations in patients with porphyria cutanea tarda in the Czech Republic2008 | Third Faculty of Medicine
- Prevalence of HFE gene C282Y and H63D mutations and elevated iron biochemistries in patients with non-alcoholic fatty liver and alcoholic liver disease2004 | Third Faculty of Medicine
- The HFE mutation in patogenesis of the alcoholic steatofibrosis and non-alcoholic steatosisPublication without faculty affiliation
- Mutation of the HFE gene in patients with hereditary hemochromatosis and other diseases with iron accumulation in the liver2002 | Third Faculty of Medicine
- Hereditary hemochromatosis: Detection of C282Y and H63D mutations in HFE gene by means of guthrie cards in population of Czech Republic2002 | Third Faculty of Medicine
- HFE gene mutations in non-alcoholic steatohepatitis and alcoholic liver diseasePublication without faculty affiliation
- Role of mutations of HFE gene in non alcoholic steatohepatitis and alcoholic liver diseasePublication without faculty affiliation
- S65C and other mutations in the Haemochromatosis gene in the Czech population2005 | Third Faculty of Medicine, Faculty of Physical Education and Sport
- Therapeutic erytrocytapheresis in the initial treatment of hereditary hemochromatosis2012 | Faculty of Medicine in Hradec Králové
- Hemochromatosis2010 | Third Faculty of Medicine
- Multiplex Dideoxynucleotide Sequencing Using Polyadenylated Sequencing Primers Multiplex Dideoxynucleotide Sequencing Using Polyadenylated Sequencing Primers2013 | Faculty of Medicine in Hradec Králové
- Thermal stabilisation of the short DNA duplexes by acridine-4-carboxamide derivatives2022 | Faculty of Pharmacy in Hradec Králové
- Lack of association of iron metabolism and Dupuytren's disease2008 | First Faculty of Medicine, Third Faculty of Medicine
- Diabetes mellitus and molecular genetic consequences2006 | Second Faculty of Medicine
- Hemochromatosis. Determination of the C282Y mutation frequency in the population of the Czech Republic and sensitivity of hemochromatosis detection using Guthrie cards1999 | First Faculty of Medicine, Third Faculty of Medicine
- Is tamoxifen porfynogenic?2005 | Third Faculty of Medicine
- Liver HFE protein content is posttranscriptionally decreased in iron-deficient mice and rats2018 | First Faculty of Medicine, Faculty of Physical Education and Sport