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International Journal of Pediatric Obesity : IJPO : an Official Journal of the International Association for the Study of Obesity|September 13, 2011
Does obesity lead to a specific lipid disorder? Analysis from the German/Austrian/Swiss APV registryReinhard W Holl, Ulrike Hoffmeister, Michael Thamm, et al.
The Journal of Clinical Endocrinology and Metabolism|May 27, 2010
A new phenotype of nongoitrous and nonautoimmune hyperthyroidism caused by a heterozygous thyrotropin receptor mutation in transmembrane helix 6Franziska Winkler, Gunnar Kleinau, Patrick Tarnow, et al.
Hormone Research in Paediatrics|May 14, 2015
The Aldosterone/Renin Ratio as a Diagnostic Tool for the Diagnosis of Primary Hypoaldosteronism in Newborns and InfantsBeate Ruecker, Mariarosaria Lang-Muritano, Katharina Spanaus, et al.
Journal of Pharmacokinetics and Pharmacodynamics|June 12, 2021
Modeling of levothyroxine in newborns and infants with congenital hypothyroidism: challenges and opportunities of a rare disease multi-center studyGilbert Koch, Britta Steffens, Stephanie Leroux, et al.
Frontiers in Medicine|May 19, 2023
Clinically practical pharmacometrics computer model to evaluate and personalize pharmacotherapy in pediatric rare diseases: application to Graves' diseaseBritta Steffens, Gilbert Koch, Pascal Gächter, et al.
Scientific Reports|December 16, 2025
Ultrasound-measured enlargement of the cross-sectional area of the median nerve as a marker for early neuronal lesions in pediatric type 1 diabetesMiriam C Eilers, Metsnanat Fellmann, Dagmar l'Allemand, et al.
Journal of the Endocrine Society|July 2, 2025
Prevalence of Differences of Sex Development Among Pediatric Endocrine Care Centers in Switzerland From 2000 to 2019Sara Metzger, Christine Aebi-Ochsner, Kanetee Busiah, et al.
Science Translational Medicine|October 5, 2022
NOS1 mutations cause hypogonadotropic hypogonadism with sensory and cognitive deficits that can be reversed in infantile miceKonstantina Chachlaki, Andrea Messina, Virginia Delli, et al.
European Journal of Endocrinology|February 9, 2018
Congenital hypogonadotropic hypogonadism and constitutional delay of growth and puberty have distinct genetic architecturesDaniele Cassatella, Sasha R Howard, James S Acierno, et al.
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