Publications by authors named "M Snajderova"

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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, Klara Maratova, Julia Martinkova, Marta Snajderova

Eur J Pediatr· June 2025

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Early-onset growth hormone treatment in Prader-Willi syndrome attenuates transition to severe obesity.
Aneta Kodytková, Shenali Anne Amaratunga, Eva El-Lababidi, Ivana Čermáková, Jana Černá

J Pediatr Endocrinol Metab· May 2025

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Variant pubertal development in Prader-Willi syndrome: early and slow progression of pubarche with normal age at gonadarche.
Aneta Kodytková, Petra Dušátková, Shenali Anne Amaratunga, Stanislava Koloušková, Barbora Obermannová

Front Endocrinol (Lausanne)· April 2025

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Genetic Testing of Children With Familial Tall Stature: Is it Worth Doing?
Katerina Gregorova, Lukas Plachy, Petra Dusatkova, Klara Maratova, Vit Neuman, Marta Snajderova

J Clin Endocrinol Metab· October 2024

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Etiology of combined pituitary hormone deficiency: GNAO1 as a novel candidate gene.
Lukas Plachy, Petra Dusatkova, Klara Maratova, Shenali Anne Amaratunga, Dana Zemkova, Marta Snajderova

Endocr Connect· October 2024

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