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The Journal of Clinical Endocrinology and Metabolism|April 5, 2013
Management of differentiated thyroid cancer in the presence of resistance to thyroid hormone and TSH-secreting adenomas: a report of four cases and review of the literatureUğur Ünlütürk, Chutintorn Sriphrapradang, Murat Faik Erdoğan, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|March 5, 2013
A clinically euthyroid child with a large goiter due to a thyroglobulin gene defect: clinical features and genetic studiesPia Hermanns, Samuel Refetoff, Chutintorn Sriphrapradang, 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.Thyroid : Official Journal of the American Thyroid Association|January 12, 2013
Two cases of thyroid dysgenesis caused by different novel PAX8 mutations in the DNA-binding region: in vitro studies reveal different pathogenic mechanismsPia Hermanns, Helmut Grasberger, Ronald Cohen, et al.Cancer Research|April 9, 2009
Oncogenic Kras requires simultaneous PI3K signaling to induce ERK activation and transform thyroid epithelial cells in vivoKelly A Miller, Nicole Yeager, Kristen Baker, et al.American Journal of Clinical Pathology|September 20, 2021
Triiodothyroacetic Acid Cross-Reacts With Measurement of Triiodothyronine (T3) on Various Immunoassay PlatformsSiaw Li Chan, Samuel Refetoff, Nikolina Babic, et al.Molecular Endocrinology (Baltimore, Md.)|August 21, 2004
Delineation of the discontinuous-conformational epitope of a monoclonal antibody displaying full in vitro and in vivo thyrotropin activitySabine Costagliola, Marco Bonomi, Nils G Morgenthaler, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|July 29, 2008
Congenital neonatal hyperthyroidism caused by germline mutations in the TSH receptor geneJeremy Chester, Deborah Rotenstein, Usanee Ringkananont, et al.Plos One|July 21, 2020
Intranasal delivery of Thyroid hormones in MCT8 deficiencyCarmen Grijota-Martínez, Soledad Bárez-López, Eva Ausó, et al.International Journal of Pediatric Endocrinology|April 16, 2015
A new family with an activating mutation (G431S) in the TSH receptor gene: a phenotype discussion and review of the literatureCæcilie C Larsen, Lefkothea P Karaviti, Victor Seghers, et al.Pageof 21