- Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY)2010 | Second Faculty of Medicine
- Neonatal Diabetes Mellitus Caused by Activation Mutation in the Gene Encoding the Kir6.2 Subunit of Potassium Channel: Is Insulindependency Inevitably Life-long?2005 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport, Third Faculty of Medicine
- Sulphonylurea treatment does not improve psychomotor development in children with KCNJ11 mutations causing permanent neonatal diabetes mellitus accompanied by developmental delay and epilepsy (DEND syndrome)2007 | Second Faculty of Medicine
- Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia2012 | Faculty of Medicine in Pilsen
- Clinical Heterogeneity in Patients With FOXP3 Mutations Presenting With Permanent Neonatal Diabetes2009 | Second Faculty of Medicine
- Implication of different replicons in the spread of the VIM-1-encoding integron, In110, in Enterobacterales from Czech hospitals2023 | Faculty of Medicine in Pilsen, Third Faculty of Medicine