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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.
Antioxidants & Redox Signaling|September 23, 2009
The syndrome of inherited partial SBP2 deficiency in humansAlexandra M Dumitrescu, Caterina Di Cosmo, Xiao-Hui Liao, et al.
The Journal of Clinical Endocrinology and Metabolism|September 23, 2017
Prenatal Diagnosis of Resistance to Thyroid Hormone and Its Clinical ImplicationsTheodora Pappa, João Anselmo, Sunnee Mamanasiri, et al.
Endocrinology|June 6, 2009
A thyroid hormone analog with reduced dependence on the monocarboxylate transporter 8 for tissue transportCaterina Di Cosmo, Xiao-Hui Liao, Alexandra M Dumitrescu, 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.
Endocrinology|September 1, 2015
The Thyroid Hormone Analog DITPA Ameliorates Metabolic Parameters of Male Mice With Mct8 DeficiencyAlfonso Massimiliano Ferrara, Xiao-Hui Liao, Honggang Ye, et al.
Thyroid : Official Journal of the American Thyroid Association|October 13, 2021
Extended Absorption of Liothyronine from Poly-Zinc-Liothyronine: Results from a Phase 1, Double-Blind, Randomized, and Controlled Study in HumansAlexandra M Dumitrescu, Erin C Hanlon, Marilyn Arosemena, et al.
The Journal of Clinical Investigation|August 4, 2010
Mice deficient in MCT8 reveal a mechanism regulating thyroid hormone secretionCaterina Di Cosmo, Xiao-Hui Liao, Alexandra M Dumitrescu, et al.
Thyroid : Official Journal of the American Thyroid Association|March 7, 2009
Selenium supplementation fails to correct the selenoprotein synthesis defect in subjects with SBP2 gene mutationsLutz Schomburg, Alexandra M Dumitrescu, Xiao-Hui Liao, et al.
Thyroid : Official Journal of the American Thyroid Association|September 16, 2024
Combined Levothyroxine and Propylthiouracil Treatment in Children with Monocarboxylate Transporter 8 Deficiency: A Multicenter Case Series of 12 PatientsRoy E Weiss, Joana R N Lemos, Alexandra M Dumitrescu, et al.
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