Publications
- Late diagnosis of complete androgen insensitivity syndrome and transmission/carriers of the condition in a family with mutation c.2495G. T p.(Arg832Leu) in exon 7 of the androgen receptor gene: genetic, clinical and ethical aspects2019 | Faculty of Medicine in Pilsen, Second Faculty of Medicine
- Ultrasound cardiac output monitoring in mechanically ventilated children2021 | Faculty of Medicine in Pilsen
- Monogenic diabetes MODY in childhood: a retrospective study of patients diagnosed at the Department of Pediatrics, University Hospital in Pilsen in 2000-20172019 | Faculty of Medicine in Pilsen, Second Faculty of Medicine
- New genetic causes of primary adrenal insufficiency2018 | Faculty of Medicine in Pilsen
- Autoimmune disease, familial clustering and thyroid carcinoma coexistent with autoimmune thyroiditis in children and adolescence: A cross-sectional study from the Czech Republic2018 | Faculty of Medicine in Pilsen
- First 2 cases with thiamine-responsive megaloblastic anemia in the Czech Republic, a rare form of monogenic diabetes mellitus: a novel mutation in the thiamine transporter SLC19A2 gene-intron 1 mutation c.204+2T>G2017 | Faculty of Medicine in Pilsen
- First case report of rare congenital adrenal insufficiency caused by mutations in the CYP11A1 gene in the Czech Republic2016 | Faculty of Medicine in Pilsen
- Noninvasive hemodynamic monitoring in critically ill children - USCOM. Prospective observational study2016 | Faculty of Medicine in Pilsen
- Hypoglycaemia as a cause of unconsciousness in a 15-year-old girl2015 | Faculty of Medicine in Pilsen
- Associated autoimmune diseases in childhood +12015 | Faculty of Medicine in Pilsen
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