Jurgen Klammt

Leipzig, SN, Germany

Last Updated: 09/26/2026

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Found 21 publications

A Comprehensive Cohort Analysis Comparing Growth and GH Therapy Response in IGF1R Mutation Carriers and SGA Children.

A Comprehensive Cohort Analysis Comparing Growth and GH Therapy Response in IGF1R Mutation Carriers and SGA Children.

Journal: The Journal of clinical endocrinology and metabolism

Published: May 31, 2019

Screening a large pediatric cohort with GH deficiency for mutations in genes regulating pituitary development and GH secretion: Frequencies, phenotypes and growth outcomes.

Screening a large pediatric cohort with GH deficiency for mutations in genes regulating pituitary development and GH secretion: Frequencies, phenotypes and growth outcomes.

Journal: EBioMedicine

Published: September 12, 2018

IGF1R Gene Alterations in Children Born Small for Gestitional Age (SGA).

IGF1R Gene Alterations in Children Born Small for Gestitional Age (SGA).

Journal: Open access Macedonian journal of medical sciences

Published: August 18, 2018

Novel Mutations in the Asparagine Synthetase Gene (ASNS) Associated With Microcephaly.

Novel Mutations in the Asparagine Synthetase Gene (ASNS) Associated With Microcephaly.

Journal: Frontiers in genetics

Published: April 05, 2018

Dominant-negative STAT5B mutations cause growth hormone insensitivity with short stature and mild immune dysregulation.

Dominant-negative STAT5B mutations cause growth hormone insensitivity with short stature and mild immune dysregulation.

Journal: Nature communications

Published: June 02, 2017

Identification of SLC20A1 and SLC15A4 among other genes as potential risk factors for combined pituitary hormone deficiency.

Identification of SLC20A1 and SLC15A4 among other genes as potential risk factors for combined pituitary hormone deficiency.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: February 16, 2017

Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes.

Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes.

Journal: Journal of human genetics

Published: December 08, 2016

Copy number variations in "classical" obesity candidate genes are not frequently associated with severe early-onset obesity in children.

Copy number variations in "classical" obesity candidate genes are not frequently associated with severe early-onset obesity in children.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: November 22, 2016

Functional and clinical relevance of novel and known PCSK1 variants for childhood obesity and glucose metabolism.

Functional and clinical relevance of novel and known PCSK1 variants for childhood obesity and glucose metabolism.

Journal: Molecular metabolism

Published: October 10, 2016

Clinical and biochemical consequences of an intragenic growth hormone receptor (GHR) deletion in a large Chinese pedigree.

Clinical and biochemical consequences of an intragenic growth hormone receptor (GHR) deletion in a large Chinese pedigree.

Journal: Clinical endocrinology

Published: July 20, 2014

The interaction of glucocorticoids and progesterone distinctively affects epithelial sodium transport.

The interaction of glucocorticoids and progesterone distinctively affects epithelial sodium transport.

Journal: Lung

Published: April 08, 2014

Novel heterozygous IGF1R mutation in two brothers with developing impaired glucose tolerance.

Novel heterozygous IGF1R mutation in two brothers with developing impaired glucose tolerance.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: March 23, 2014

Showing 1-12 of 21

Last Updated: 09/26/2026