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RHI
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doc. MUDr. Ondřej Souček Ph.D.
Academic staff at Second Faculty of Medicine
46 publications
Publications
publication
Nephrotic syndrome sera induce different transcriptomes in podocytes based on the steroid response
2024 |
Second Faculty of Medicine, Central Library of Charles University, Faculty of Medicine in Pilsen
publication
Nephrotic syndrome sera induce different transcriptomes in podocytes based on the steroid response
2024 |
Second Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Genetic testing of children with familial tall stature: is it worth doing?
2024 |
Second Faculty of Medicine
publication
Adult height in children born small for gestational age (SGA) with persistent short stature (SGA-SS). Growth hormone treatment outcomes from data of the Czech countrywide REPAR database
2023 |
First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine, Third Faculty of Medicine, Faculty of Medicine in Pilsen
publication
A comprehensive validation study of the latest version of BoneXpert on a large cohort of Caucasian children and adolescents
2023 |
Faculty of Mathematics and Physics, Second Faculty of Medicine, Faculty of Science
publication
Haplotype analysis of the X chromosome in patients with Turner syndrome in order to verify the possible effect of imprinting on selected symptoms
2022 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Karyotyping of Lymphocytes and Epithelial Cells of Distinct Embryonic Origin Does Not Help to Predict the Turner Syndrome Features
2022 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Two phenotypes of chronic recurrent multifocal osteomyelitis with different patterns of bone involvement
2022 |
Second Faculty of Medicine, Central Library of Charles University
publication
Alteration in DNA-binding affinity of Wilms tumor 1 protein due to WT1 genetic variants associated with steroid - resistant nephrotic syndrome in children
2022 |
Second Faculty of Medicine
publication
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 study
2021 |
First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine
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