Publications
- Functional Analyses of HNF1A-MODY Variants Refine the Interpretation of Identified Sequence Variants2020 | Second Faculty of Medicine
- Monogenic form of autoimmune diabetes as a part of dysregulation of immune system2018 | Second Faculty of Medicine
- Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes2017 | Second Faculty of Medicine
- Hepatic phenotypes of HNF1B gene mutations: A case of neonatal cholestasis requiring portoenterostomy and literature review2015 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- 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
- Liver, kidneys and diabetes: three faces of HNF1B gene deficit2014 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Is genetic testing in children with growth hormone deficiency clinically justified?2013 | Second Faculty of Medicine
- Two Independent Genetic Factors Responsible for the Associations of the IBD5 Locus with Crohn's Disease in the Czech Population2011 | Second Faculty of Medicine
- Lack of PAX4 mutations in 53 Czech MODYX families2010 | Second Faculty of Medicine
- The CTLA4 variants may interact with the IL23R-and NOD2-conferred risk in development of Crohn's disease2010 | Second Faculty of Medicine
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