Publications
- High incidence of heterozygous ABCC8 and HNF1A mutations in Czech patients with congenital hyperinsulinism2015 | Second Faculty of Medicine, First Faculty of Medicine, Third Faculty of Medicine
- Congenital hyperinsulinism: molecular genetic background and ethiopatogenesis2014 | Second Faculty of Medicine
- Congenital hyperinsulinism: diagnostics and management2014 | Second Faculty of Medicine
- Quality of Life and Treatment Satisfaction in Participants with Maturity-Onset Diabetes of the Young: A Comparison to Other Major Forms of Diabetes2022 | Second Faculty of Medicine, Faculty of Mathematics and Physics
- 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
- Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study2020 | Second Faculty of Medicine
- Dětská mozková obrna2020 | Second Faculty of Medicine
- Poruchy vodní a elektrolytové rovnováhy u dětí: 50 let molekuly DDAVP2019 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Effectiveness and safety of the tri-iodothyronine analogue Triac in children and adults with MCT8 deficiency: an international, single-arm, open-label, phase 2 trial2019 | Second Faculty of Medicine
- Could a combination of heterozygous ABCC8 and KCNJ11 mutations cause congenital hyperinsulinism?2017 | Second Faculty of Medicine
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