Stepanka Pruhova
8PUBLICATIONS
85CO-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
|Jan 16, 2026
International guideline on genetic testing of children with short stature.Andrew Dauber, Alexander A L Jorge, Ola Nilsson
|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
|Jan 04, 2023
Monogenic diabetes mellitus hidden in autoantibody-negative diabetes mellitus.Stepanka Pruhova, Petra Dusatkova
|Dec 01, 2021
Two New Mutations in the CEL Gene Causing Diabetes and Hereditary Pancreatitis: How to Correctly Identify MODY8 Cases.Khadija El Jellas, Petra Dušátková, Ingfrid S Haldorsen
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Frequent Collaborators
5 joint publications
Petra Dusatkova
4 joint publications
Jan Lebl
3 joint publications
Barbora Obermannová
3 joint publications
Zdeněk Šumník
2 joint publications
Jirina Zapletalová
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
