Marta Snajderova

Prague, PR 15000, Czech Republic

Last Updated: 09/26/2026

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Found 27 publications

Beyond GH stimulation tests: genetic heterogeneity and treatment response in children with diagnosed GH deficiency.

Beyond GH stimulation tests: genetic heterogeneity and treatment response in children with diagnosed GH deficiency.

Journal: Journal of the Endocrine Society

Published: March 15, 2026

Noonan syndrome spectrum disorders in real life: patient characteristics and response to growth hormone therapy in a genetically defined single-country multicenter cohort.

Noonan syndrome spectrum disorders in real life: patient characteristics and response to growth hormone therapy in a genetically defined single-country multicenter cohort.

Journal: European journal of pediatrics

Published: August 20, 2025

Cytogenetic anomalies are the predominant genetic alteration in children with nonfamilial tall stature: a comparative study with familial cases.

Cytogenetic anomalies are the predominant genetic alteration in children with nonfamilial tall stature: a comparative study with familial cases.

Journal: European journal of pediatrics

Published: April 01, 2025

Variant pubertal development in Prader-Willi syndrome: early and slow progression of pubarche with normal age at gonadarche.

Variant pubertal development in Prader-Willi syndrome: early and slow progression of pubarche with normal age at gonadarche.

Journal: Frontiers in endocrinology

Published: November 12, 2024

Early-onset growth hormone treatment in Prader-Willi syndrome attenuates transition to severe obesity.

Early-onset growth hormone treatment in Prader-Willi syndrome attenuates transition to severe obesity.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: September 27, 2024

Etiology of combined pituitary hormone deficiency: GNAO1 as a novel candidate gene.

Etiology of combined pituitary hormone deficiency: GNAO1 as a novel candidate gene.

Journal: Endocrine connections

Published: May 04, 2024

Genetic Testing of Children With Familial Tall Stature: Is it Worth Doing?

Genetic Testing of Children With Familial Tall Stature: Is it Worth Doing?

Journal: The Journal of clinical endocrinology and metabolism

Published: October 24, 2023

Analysis of children with familial short stature: who should be indicated for genetic testing?

Analysis of children with familial short stature: who should be indicated for genetic testing?

Journal: Endocrine connections

Published: June 13, 2023

Isolated growth hormone deficiency in children with vertically transmitted short stature: What do the genes tell us?

Isolated growth hormone deficiency in children with vertically transmitted short stature: What do the genes tell us?

Journal: Frontiers in endocrinology

Published: November 19, 2022

The Genetic Landscape of Children Born Small for Gestational Age with Persistent Short Stature.

The Genetic Landscape of Children Born Small for Gestational Age with Persistent Short Stature.

Journal: Hormone research in paediatrics

Published: November 16, 2022

Karyotyping of Lymphocytes and Epithelial Cells of Distinct Embryonic Origin Does Not Help to Predict the Turner Syndrome Features.

Karyotyping of Lymphocytes and Epithelial Cells of Distinct Embryonic Origin Does Not Help to Predict the Turner Syndrome Features.

Journal: Hormone research in paediatrics

Published: January 07, 2022

Familial Short Stature-A Novel Phenotype of Growth Plate Collagenopathies.

Familial Short Stature-A Novel Phenotype of Growth Plate Collagenopathies.

Journal: The Journal of clinical endocrinology and metabolism

Published: October 27, 2020

Showing 1-12 of 27

Last Updated: 09/26/2026