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The Journal of Clinical Endocrinology and Metabolism|October 28, 2004
Thyroid hormone responsive genes in cultured human fibroblastsLars C Moeller, Alexandra M Dumitrescu, Robert L Walker, et al.
European Thyroid Journal|November 25, 2015
Two Novel Mutations in the Serpina7 Gene Are Associated with Complete Deficiency of Thyroxine-Binding GlobulinLars C Moeller, Yaw Appiagyei-Dankah, Birgit Köhler, et al.
Molecular Endocrinology (Baltimore, Md.)|August 9, 2003
Hypothyroidism in thyroid transcription factor 1 haploinsufficiency is caused by reduced expression of the thyroid-stimulating hormone receptorLars C Moeller, Shioko Kimura, Takashi Kusakabe, et al.
European Journal of Endocrinology|February 17, 2022
The interplay of thyroid hormones and the immune system - where we stand and why we need to know about itChristina Wenzek, Anita Boelen, Astrid M Westendorf, et al.
The Journal of Clinical Endocrinology and Metabolism|February 13, 2015
Successful treatment of type B insulin resistance with rituximabEmmanouil-Dimitrios Manikas, Iona Isaac, Robert K Semple, et al.
Endocrine Connections|February 18, 2026
Digital vs. Conventional Glycemic Monitoring in Rare Endocrine Cancers: Comparison of Effectiveness During ChemotherapyLukas van Baal, Harald Lahner, Jasna Pavlovic, et al.
European Thyroid Journal|November 25, 2015
Differences in Mouse Hepatic Thyroid Hormone Transporter Expression with Age and HyperthyroidismKathrin Engels, Helena Rakov, Denise Zwanziger, et al.
The Journal of Clinical Endocrinology and Metabolism|May 6, 2004
Partial deficiency of thyroxine-binding globulin-Allentown is due to a mutation in the signal peptideAnja Fingerhut, Sirimon Reutrakul, Sebastian D Knuedeler, et al.
The Journal of Clinical Endocrinology and Metabolism|June 1, 2006
C-terminal amino acid alteration rather than late termination causes complete deficiency of thyroxine-binding globulin CD-NeuIsenburgLars C Moeller, Anja Fingerhut, Harald Lahner, et al.
Thyroid : Official Journal of the American Thyroid Association|June 18, 2020
A Novel Double RET E768D/L790F Mutation Associated with a MEN2B-Like PhenotypeAnnie Mathew, Soeren Latteyer, Karin Frank-Raue, et al.
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