Barbora Obermannová

3PUBLICATIONS
35CO-AUTHORS
NanomedicineNeurogeneticsInfant and child health
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Publications (3)

|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

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Frequent Collaborators

3 joint publications

Zdeněk Šumník

3 joint publications

Jan Lebl

3 joint publications

Štěpánka Průhová

2 joint publications

Marta Šnajderová