- 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
- Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia2012 | Faculty of Medicine in Pilsen
- Pharmacogenomics in diabetes: outcomes of thiamine therapy in TRMA syndrome2018 | Faculty of Medicine in Pilsen