Publikace
- Genetic testing of children with familial tall stature: is it worth doing?2024 | 2. lékařská fakulta
- Haplotype analysis of the X chromosome in patients with Turner syndrome in order to verify the possible effect of imprinting on selected symptoms2022 | 1. lékařská fakulta, 2. lékařská fakulta
- Karyotyping of Lymphocytes and Epithelial Cells of Distinct Embryonic Origin Does Not Help to Predict the Turner Syndrome Features2022 | 1. lékařská fakulta, 2. lékařská fakulta
- Novel presentation of the c.1856A > G (p.Asp619Gly) TSHR gene-activating variant: relapsing hyperthyroidism in three subsequent generations manifesting in early childhood and an in vitro functional study2021 | 1. lékařská fakulta, 2. lékařská fakulta, 3. lékařská fakulta
- Moderní diagnostika osteoporózy a hodnocení rizika fraktur u dívek s Turnerovým syndromem2017 | 2. lékařská fakulta
- The muscle-bone interaction in Turner syndrome2015 | Matematicko-fyzikální fakulta, 2. lékařská fakulta
- Muscle function in Turner syndrome: normal force but decreased power2015 | Matematicko-fyzikální fakulta, 2. lékařská fakulta
- Artificially low cortical bone mineral density in Turner syndrome is due to the partial volume effect2015 | 2. lékařská fakulta
- Hypophosphatasia due to uniparental disomy2015 | 2. lékařská fakulta
- Boys with haemophilia have low trabecular bone mineral density and sarcopenia, but normal bone strength at the radius2012 | 2. lékařská fakulta
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