- Genetic hemochromatosis2002 | Third Faculty of Medicine
- Hemochromatosis2010 | Third Faculty of Medicine
- Neonatal hemochromatosis2018 | First Faculty of Medicine, Second Faculty of Medicine
- Mutation of the HFE gene in patients with hereditary hemochromatosis and other diseases with iron accumulation in the liver2002 | Third Faculty of Medicine
- Hemochromatosis2003 | First 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
- Diagnostic and therapeutic guidelines in genetic hemochromatosis. Guidelines of the Czech Society of Hepatology of the Czech Medical Association J. E. Purkyne2006 | Third Faculty of Medicine
- Chelating Polymers for Hereditary Hemochromatosis Treatment2020 | First Faculty of Medicine, Central Library of Charles University, Faculty of Science
- Neonatal hemochromatosis associated with renal tubular dysgenesis2014 | Faculty of Medicine in Hradec Králové
- Therapeutic erytrocytapheresis in the initial treatment of hereditary hemochromatosis2012 | Faculty of Medicine in Hradec Králové
- Hemochromatosis and her joint manifestationsPublication without faculty affiliation
- Neonatal (Perinatal) Hemochromatosis2001 | First Faculty of Medicine
- How difficult is diagnosis of hemochromatosisPublication without faculty affiliation
- Neonatal (perinatal) hemochromatosis2001 | Faculty of Medicine in Pilsen, Central Library of Charles University
- 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
- Is the diagnosis of the primary hemochromatosis really easy?Publication without faculty affiliation
- 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
- Multiple erythrocytapheresis in therapy of hereditary hemochromatosisPublication without faculty affiliation
- Hemochromatosis-inherited disease of iron metabolismusPublication without faculty affiliation
- The hemochromatosis protein HFE signals predominantly via the BMP type I receptor ALK3 in vivo2018 | First Faculty of Medicine
- Decrease of irou stores in hereditary hemochromatosis patients +1Publication without faculty affiliation
- Monitoring of liver iron levels in the patients with hemochromatosisPublication without faculty affiliation
- Red cell apheresis in therapy of hereditary hemochromatosisPublication without faculty affiliation
- Decrease of ferritin in hereditary hemochromatosis patients treated with erythorcytapheresis +1Publication without faculty affiliation
- Elimination of iron in hereditary hemochromatosis patients treated with erythrocytapheresisPublication without faculty affiliation
- Erythrocytapheresis in hereditary hemochromatosis patients. A study of iron eliminationPublication without faculty affiliation
- Multiple red cell apheresis in therapy of hereditary hemochromatosisPublication without faculty affiliation
- Duodenal expression of iron transport molecules in patients with hereditary hemochromatosis or iron deficiency2012 | First Faculty of Medicine, Faculty of Medicine in Pilsen, Third Faculty of Medicine