- Mutations in the gene encoding the Kir6.2 calcium channel subunit as another onset of neonatal diabetes2006 | Second 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
- KCNJ11 E23K polymorphism and diabetes mellitus with adult onset in Czech patients2007 | Third 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 | Third Faculty of Medicine, Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Congenital hyperinsulinism caused by novel homozygous katp channel gene variants may be linked to unexplained neonatal deaths among kurdish consanguineous families2020 | Second Faculty of Medicine
- Could a combination of heterozygous ABCC8 and KCNJ11 mutations cause congenital hyperinsulinism?2017 | Second Faculty of Medicine
- Activating Mutations in the Gene Encoding the ATP-Sensitive Potassium-Channel Subunit Kir6.2 and Permanent Neonatal Diabetes2004 | Second Faculty of Medicine