Jan Lebl
8PUBLICATIONS
206CO-AUTHORS

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Publications (8)
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|Jan 23, 2026
Noonan syndrome spectrum disorders in real life: patient characteristics and response to growth hormone therapy in a genetically defined single-country multicenter cohort.Barbora Jirova, Maria Najdekova, Jana Cerna
|Jun 16, 2025
Cytogenetic anomalies are the predominant genetic alteration in children with nonfamilial tall stature: a comparative study with familial cases.Katerina Gregorova, Lukas Plachy, Petra Dusatkova
|Mar 13, 2025
Early-onset growth hormone treatment in Prader-Willi syndrome attenuates transition to severe obesity.Aneta Kodytková, Shenali Anne Amaratunga, Eva El-Lababidi
|Mar 13, 2025
Mapping variants in thyroid hormone transporter MCT8 to disease severity by genomic, phenotypic, functional, structural and deep learning integration.Stefan Groeneweg, Ferdy S van Geest, Mariano Martín
|Nov 22, 2024
Heterozygous BTNL8 variants in individuals with multisystem inflammatory syndrome in children (MIS-C).Evangelos Bellos, Dilys Santillo, Pierre Vantourout
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Frequent Collaborators
4 joint publications
Stepanka Pruhova
3 joint publications
Barbora Obermannová
3 joint publications
Petra Dusatkova
3 joint publications
Zdeněk Šumník
2 joint publications
Shenali Anne Amaratunga
2 joint publications
Dana Novotná
2 joint publications
Marta Šnajderová
2 joint publications
Jiří Strnadel
2 joint publications
Ivana Kotvalová
2 joint publications
Stanislava Koloušková