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Thyroid : Official Journal of the American Thyroid Association|April 3, 2019
Reduced Sensitivity to Thyroid Hormone as a Transgenerational Epigenetic Marker Transmitted Along the Human Male LineJoão Anselmo, Neal H Scherberg, Alexandra M Dumitrescu, et al.Thyroid : Official Journal of the American Thyroid Association|November 17, 2020
Early Diagnosis and Treatment of an Infant with a Novel Thyroid Hormone Receptor α Gene (pC380SfsX9) MutationAry E Furman, Alexandra M Dumitrescu, Samuel Refetoff, et al.Journal of Neurology|April 19, 2005
X-linked paroxysmal dyskinesia and severe global retardation caused by defective MCT8 geneKnut Brockmann, Alexandra M Dumitrescu, Thomas T Best, et al.Endocrinology|October 14, 2017
Thyroid Hormone Metabolism Defects in a Mouse Model of SBP2 DeficiencyJiao Fu, Haruki Fujisawa, Benjamin Follman, et al.Thyroid : Official Journal of the American Thyroid Association|April 21, 2018
Homozygous Mutation in Human Serum Albumin and Its Implication on Thyroid TestsMizuho S Mimoto, Anara Karaca, Neal Scherberg, et al.Nuclear Receptor Signaling|July 25, 2006
Thyroid hormone mediated changes in gene expression can be initiated by cytosolic action of the thyroid hormone receptor beta through the phosphatidylinositol 3-kinase pathwayLars C Moeller, Xia Cao, Alexandra M Dumitrescu, et al.Endocrinology|December 12, 2019
Role of the Thyroid Gland in Expression of the Thyroid Phenotype of Sbp2-Deficient MiceHaruki Fujisawa, Manassawee Korwutthikulrangsri, Jiao Fu, et al.Endocrinology|May 20, 2006
Tissue-specific thyroid hormone deprivation and excess in monocarboxylate transporter (mct) 8-deficient miceAlexandra M Dumitrescu, Xiao-Hui Liao, Roy E Weiss, et al.American Journal of Human Genetics|December 9, 2003
A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter geneAlexandra M Dumitrescu, Xiao-Hui Liao, Thomas B Best, et al.Thyroid : Official Journal of the American Thyroid Association|May 25, 2022
A Novel Pathogenic Variant in PAX8 Leads to Familial Congenital HypothyroidismMonica Malheiros França, Lucy Reeve, Alexandra M Dumitrescu, et al.Pageof 7