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Endocrinology|January 29, 2000
The 3',5'-cyclic adenosine monophosphate response element binding protein (CREB) is functionally reduced in human toxic thyroid adenomasA Brunetti, E Chiefari, S Filetti, et al.
Forum (Genoa, Italy)|July 1, 1999
Thyrotropin receptor: a role for thyroid tumourigenesis?D Russo, F Arturi, E Chiefari, et al.
Journal of Endocrinological Investigation|March 12, 2017
Gestational diabetes mellitus: an updated overviewE Chiefari, B Arcidiacono, D Foti, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|August 26, 1998
Thyroid hyperfunctioning adenomas with and without Gsp/TSH receptor mutations show similar clinical featuresF Arturi, C Capula, E Chiefari, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 7, 2001
Transcriptional regulation of human insulin receptor gene by the high-mobility group protein HMGI(Y)A Brunetti, G Manfioletti, E Chiefari, et al.
The Journal of Clinical Endocrinology and Metabolism|November 30, 2000
A novel mutation in the thyrotropin (TSH) receptor gene causing loss of TSH binding but constitutive receptor activation in a family with resistance to TSHD Russo, C Betterle, F Arturi, et al.
The Journal of Clinical Endocrinology and Metabolism|November 5, 1997
A case of metastatic medullary thyroid carcinoma: early identification before surgery of an RET proto-oncogene somatic mutation in fine-needle aspirate specimensD Russo, F Arturi, E Chiefari, et al.
European Journal of Endocrinology|May 7, 1999
Iodide symporter gene expression in normal and transformed rat thyroid cellsF Trapasso, R Iuliano, E Chiefari, et al.
Thyroid : Official Journal of the American Thyroid Association|December 29, 2000
A Phe 486 thyrotropin receptor mutation in an autonomously functioning follicular carcinoma that was causing hyperthyroidismP Camacho, D Gordon, E Chiefari, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|March 31, 2001
A large family with hereditary MTC: role of RET genetic analysis in differential diagnosis between MEN 2A and FMTCE Chiefari, R Chiarella, U Crocetti, et al.
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