Publications
- Modern diagnosis of osteoporosis and assessment of fracture risk in girls with Turner syndrome2017 | Second Faculty of Medicine
- SALL4 phenotype in four generations of one family: An interplay of the upper limb, kidneys, and the pituitary2024 | Second Faculty of Medicine
- Genetic testing of children with familial tall stature: is it worth doing?2024 | Second Faculty of Medicine
- A comprehensive validation study of the latest version of BoneXpert on a large cohort of Caucasian children and adolescents2023 | Second Faculty of Medicine, Faculty of Mathematics and Physics, Faculty of Science
- Isolated growth hormone deficiency in children with vertically transmitted short stature: What do the genes tell us?2023 | Second Faculty of Medicine
- Analysis of children with familial short stature: who should be indicated for genetic testing?2023 | Second Faculty of Medicine
- Familial short stature - a novel phenotype of growth plate collagenopathies2021 | Second Faculty of Medicine
- It won't work the usual way - first steps with the new treatment of X-linked hypophosphatemia2021 | Second Faculty of Medicine
- NPR2 Variants Are Frequent among Children with Familiar Short Stature and Respond Well to Growth Hormone Therapy2020 | Second Faculty of Medicine
- Onemocnění skeletu u dětí2019 | Second Faculty of Medicine, First Faculty of Medicine, Third Faculty of Medicine
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