Jan Lebl

Prague, PR, Czech Republic

Last Updated: 09/26/2026

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Found 102 publications

Long-acting growth hormone: An updated Growth Hormone Research Society consensus statement.

Long-acting growth hormone: An updated Growth Hormone Research Society consensus statement.

Journal: European journal of endocrinology

Published: May 06, 2026

Integrated cardiac, endocrine, and genetic assessment in adolescent basketball players.

Integrated cardiac, endocrine, and genetic assessment in adolescent basketball players.

Journal: Frontiers in endocrinology

Published: April 09, 2026

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

Growth hormone therapy in children born small for gestational age with persistent short stature (SGA-SS): Lessons learned from real-world international databases and directions for future research.

Growth hormone therapy in children born small for gestational age with persistent short stature (SGA-SS): Lessons learned from real-world international databases and directions for future research.

Journal: Hormone research in paediatrics

Published: March 05, 2026

High prevalence of maturity-onset diabetes of the young in the Czech Republic: A 25-year nationwide registry-based study.

High prevalence of maturity-onset diabetes of the young in the Czech Republic: A 25-year nationwide registry-based study.

Journal: Diabetic medicine : a journal of the British Diabetic Association

Published: October 17, 2025

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

Investigation of glucosuria in children.

Investigation of glucosuria in children.

Journal: Minerva pediatrics

Published: December 09, 2024

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

Monogenic causes of familial short stature.

Monogenic causes of familial short stature.

Journal: Frontiers in endocrinology

Published: October 04, 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

Showing 1-12 of 102

Last Updated: 09/26/2026