- Mutations in the gene encoding the Kir6.2 calcium channel subunit as another onset of neonatal diabetes2006 | 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
- Familial mild hyperglycemia associated with a novel ABCC8-V84I mutation within three generations2011 | Second Faculty of Medicine, Third Faculty of Medicine
- A defined heteromeric K(V)1 channel stabilizes the intrinsic pacemaking and regulates the output of deep cerebellar nuclear neurons to thalamic targets2013 | Central Library of Charles University
- High incidence of heterozygous ABCC8 and HNF1A mutations in Czech patients with congenital hyperinsulinism2015 | Second Faculty of Medicine, Third Faculty of Medicine, First Faculty of Medicine
- Temporal patterns of electrical remodeling in canine ventricular hypertrophy: Focus on IKs downregulation and blunted ß-adrenergic activation2006 | Faculty of Medicine in Pilsen
- Temporal patterns of electrical remodeling in canine ventricular hypertrophy: Focus on IKs downregulation and blunted ß-adrenergic activation2006 | Faculty of Medicine in Pilsen, First Faculty of Medicine
- Congenital hyperinsulinism: Loss of B-cell self-control2016 | Second Faculty of Medicine
- Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies2018 | Second Faculty of Medicine
- Could a combination of heterozygous ABCC8 and KCNJ11 mutations cause congenital hyperinsulinism?2017 | Second Faculty of Medicine
- Broad-range TRP channel inhibitors (2-APB, flufenamic acid, SKF-96365) affect differently contraction of resistance and conduit femoral arteries of rat2015 | Faculty of Science
- 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