Publications
- High Prevalence of Growth Plate Gene Variants in Children With Familial Short Stature Treated With GH2019 | Second Faculty of Medicine
- Screening of monogenic autoimmune diabetes among children with type 1 diabetes and multiple autoimmune diseases: is it worth doing?2019 | Second Faculty of Medicine
- Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes2017 | Second Faculty of Medicine
- Novel calcium-sensing receptor cytoplasmic tail deletion mutation causing autosomal dominant hypocalcemia: molecular and clinical study2016 | Second Faculty of Medicine
- High incidence of heterozygous ABCC8 and HNF1A mutations in Czech patients with congenital hyperinsulinism2015 | First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine
- Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY)2010 | Second Faculty of Medicine
- Clinical Importance of Identification of PROP1 Gene Mutations in Children with Inherited Growth Hormone Deficiency2009 | Second Faculty of Medicine
- Glycemic control by treatment modalities: national registry-based population data in children and adolescents with type 1 diabetes2024 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine, Third Faculty of Medicine, Faculty of Mathematics and Physics, Faculty of Medicine in Hradec Králové
- Introduction of continuous glucose monitoring (CGM) is a key factor in decreasing HbA1c in war refugee children with type 1 diabetes2024 | First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine, Central Library of Charles University
- The genetic landscape of children born small for gestational age with persistent short stature (SGA-SS)2024 | Second Faculty of Medicine
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