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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|February 10, 2012
Homozygous thyroid hormone receptor β-gene mutations in resistance to thyroid hormone: three new cases and review of the literatureAlfonso Massimiliano Ferrara, Kazumichi Onigata, Oya Ercan, et al.
Hormones (Athens, Greece)|February 22, 2017
A new TRβ mutation in resistance to thyroid hormone syndromeCorina Neamţu, Claudiu Ţupea, Diana Păun, et al.
The Journal of Clinical Endocrinology and Metabolism|March 13, 2002
Complete thyroxine-binding globulin (TBG) deficiency in two families without mutations in coding or promoter regions of the TBG genes: in vitro demonstration of exon skippingSirimon Reutrakul, Alexandra Dumitrescu, Paolo E Macchia, et al.
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.
Thyroid : Official Journal of the American Thyroid Association|December 12, 2019
Free Thyroxine Concentrations in Sera of Individuals with Familial Dysalbuminemic Hyperthyroxinemia: A Comparison of Three Methods of MeasurementSamuel Refetoff, Neal H Scherberg, Chao Yuan, et al.
Nature Genetics|May 7, 2024
STR mutations on chromosome 15q cause thyrotropin resistance by activating a primate-specific enhancer of MIR7-2/MIR1179Helmut Grasberger, Alexandra M Dumitrescu, Xiao-Hui Liao, et al.
Thyroid : Official Journal of the American Thyroid Association|May 15, 2004
Familial juvenile autoimmune hypothyroidism, pituitary enlargement, obesity, and insulin resistanceSirimon Reutrakul, Eba H Hathout, Donald Janner, et al.
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