Publications
- First 2 cases with thiamine-responsive megaloblastic anemia in the Czech Republic, a rare form of monogenic diabetes mellitus: a novel mutation in the thiamine transporter SLC19A2 gene-intron 1 mutation c.204+2T>G2017 | Faculty of Medicine in Pilsen
- Extremely hypotrophic newborn of mother with systemic lupus erythematosus and antiphospholipid syndrome2014 | Faculty of Medicine in Pilsen
- Home oxygenotherapy in children with chronic lung disease2004 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Home oxygenotherapy in children with chronic lung disease2004 | Faculty of Medicine in Pilsen
- A rare cause of intrauterine and postnatal growth restriction in a full-term infant2019 | Faculty of Medicine in Pilsen
- New genetic causes of primary adrenal insufficiency2018 | Faculty of Medicine in Pilsen
- Pyridoxine-dependent Epilepsy - Case Reports2017 | Faculty of Medicine in Pilsen
- Newborn with collection of fluid in the anterior mediastinum - a casuist2017 | Faculty of Medicine in Pilsen
- First case report of rare congenital adrenal insufficiency caused by mutations in the CYP11A1 gene in the Czech Republic2016 | Faculty of Medicine in Pilsen
- The importance of continuity in the care for premature and risk infants at NICU and during follow-up2015 | First Faculty of Medicine, Faculty of Medicine in Pilsen
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