Georgia Lahr
Ulm, BW, Germany
Last Updated: 09/26/2026
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Found 10 publications
Prevalence and phenotypic characterization of MC4R variants in a large pediatric cohort.
Journal: International journal of obesity (2005)
Published: December 08, 2015
Severe Early-Onset Obesity Due to Bioinactive Leptin Caused by a p.N103K Mutation in the Leptin Gene.
Journal: The Journal of clinical endocrinology and metabolism
Published: July 18, 2015
Unmistakable Morphology? Infantile Malignant Osteopetrosis Resembling Juvenile Myelomonocytic Leukemia in Infants.
Journal: The Journal of pediatrics
Published: February 05, 2015
Biologically inactive leptin and early-onset extreme obesity.
Journal: The New England journal of medicine
Published: January 01, 2015
Successful HLA haploidentical hematopoietic SCT in chronic granulomatous disease.
Journal: Bone marrow transplantation
Published: June 24, 2014
Monogenic forms of childhood obesity due to mutations in the leptin gene.
Journal: Molecular and cellular pediatrics
Published: May 08, 2014
Age-of-onset-dependent influence of NOD2 gene variants on disease behaviour and treatment in Crohn's disease.
Journal: BMC gastroenterology
Published: August 07, 2012
A novel missense mutation in the CLCN7 gene linked to benign autosomal dominant osteopetrosis: a case series.
Journal: Journal of medical case reports
Published: April 21, 2012
Infantile malignant osteopetrosis: a rare cause of neonatal hypocalcemia.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: February 06, 2012
Loss of enteroendocrine cells in autoimmune-polyendocrine-candidiasis-ectodermal-dystrophy (APECED) syndrome with gastrointestinal dysfunction.
Journal: The Journal of clinical endocrinology and metabolism
Published: December 14, 2011
Showing 1-10 of 10
Last Updated: 09/26/2026