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CHIEFARI, EUSEBIO DOMENICO ANDREA FERNANDO

CHIEFARI, EUSEBIO DOMENICO ANDREA FERNANDO  

Dipartimento di Scienze della Salute  

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Titolo Data di pubblicazione Autore(i) File
2-s2.0-85151325029 1-gen-2022 Greco, M; Chiefari, E; Mirabelli, M; Salatino, A; Tocci, V; Cianfrone, P; Foti, D. P.; Brunetti, A.
A case of metastatic medullary thyroid carcinoma: early identification before surgery of a ret proto-oncogene somatic mutation in fine needle aspirate specimen 1-gen-1997 Russo, D.; Chiefari, E.; Meringolo, D.; Bianchi, D.; Bellanova, B.; Filetti, S.; Arturi, F
A case of metastatic medullary thyroid carcinoma: Early identification before surgery of an RET proto-oncogene somatic mutation in fine-needle aspirate specimens 1-gen-1997 Russo, D.; Arturi, F.; Chiefari, E.; Meringolo, D.; Bianchi, D.; Bellanova, B.; Filetti, S.
A hyperfunctioning Hurtle cell thyroid carcinoma with a mutation in the thyrotropin receptor 1-gen-1997 Russo, D.; Arturi, F; Chiefari, E.; Wong, M. G.; Crocetti, U.; Costante, G.; Clark, O. H.; Filetti, S.
A large family with hereditary MTC: role of RET genetic analysis in differential diagnosis between MEN 2A and FMTC 1-gen-2001 Chiefari, E.; Chiarella, R.; Tardio, B.; Arturi, F; Trischitta, V.; Filetti, S.; Zingrillo, M.; Russo, D.
A modified quantitative EMSA and its application in the study of RNA-protein interactions 1-gen-2008 G., Covello; E., Chiefari; F., Paonessa; A., Nocera; I., LE PERA; S., Iiritano; D., Foti; Brunetti, A
A new predictive tool for the early risk assessment of gestational diabetes mellitus 1-gen-2016 Capula, C; Chiefari, E; Borelli, M; Oliverio, R; Vero, A; Foti, D; Puccio, L; Vero, R; Brunetti, Antonio
A novel mechanism of post-translational modulation of HMGA functions by the histone chaperone nucleophosmin 1-gen-2015 Arnoldo, L; Sgarra, R; Chiefari, E; Iiritano, S; Arcidiacono, B; Pegoraro, S; Pellarin, I; Brunetti, A; Manfioletti, G
A novel mutation in the thyrotropin (TSH) receptor gene causing loss of TSH binding but constitutive receptor activation in a family with resistance to TSH 1-gen-2000 Russo, D.; Betterle, C.; Arturi, F.; Chiefari, E.; Girelli, M. E.; Filetti, S.
A novel mutation in the Thyrotropin receptor gene causing loss of TSH binding but constitutive activation in a family with resistance to TSH 1-gen-2000 Russo, D.; Betterle, C.; Arturi, F.; Chiefari, E.; Girelli, M. E.; Filetti, S.
A novel mutation in the thyrotropin receptor gene causing loss of TSH binding but constitutive receptor activation in a family with resistence to TSH 1-gen-2000 Russo, D.; Betterle, C.; Arturi, F; Chiefari, E.; Girelli, M. E.; Filetti, S.
A nucleoprotein complex containing Sp1, C/EBP beta, and HMGI-Y controls human insulin gene transcription 1-gen-2003 Foti, D.; Iuliano, R; Chiefari, E.; Brunetti, A.
A nucleoprotein complex containing Sp1, C/EBP beta, and HMGI-Y controls human insulin receptor gene transcription 1-gen-2003 Foti, Daniela; Iuliano, Rodolfo; Chiefari, Eusebio; Brunetti, Antonio
A nucleoprotein complex containing Sp1, C/EBPb, and HMGI(Y) controls human insulin receptor gene transcription 1-gen-2003 Foti, D.; Iuliano, R; Chiefari, E; Brunetti, A
A Nucleoprotein Complex Containing Sp1, C/EBPß, and HMGI-Y controls Human Insulin Receptor Gene Transcription 1-gen-2003 Daniela, Foti; Rodolfo, Iuliano; Eusebio, Chiefari; Brunetti, A
A Partial Phenotype of adFNDI Related to the Signal Peptide c.55G>A Variant of the AVP Gene 1-gen-2021 Tocci, Vera; Mirabelli, Maria; Giuliano, Stefania; Chiefari, Eusebio; Hagelskjær Knudsen, Jane; Kvistgaard, Helene; La Torre, Domenico; Aversa, Antonio; Foti, Daniela Patrizia; Hvarregaard Christensen, Jane; Brunetti, Antonio
A Phe 486 thyrotropin receptor mutation in an autonomously functioning follicular carcinoma that was causing hyperthyroidism 1-gen-2000 Camacho, P.; Gordon, D.; Chiefari, E.; Yong, S.; Dejong, S.; Pitale, S.; Russo, D.; Filetti, S.
A Phe 486 TSH receptor mutation in a autonomously functioning follicular carcinoma that was causing hyperthyroidism 1-gen-2000 Camacho, P.; Gordon, D; Chiefari, E.; Yong, S.; Dejong, S.; Pitale, S.; Russo, D.; Filetti, S.
A polymorphism of HMGA1 is associated with increased risk of metabolic syndrome and related components 1-gen-2013 Chiefari, E; Tanyolaç, S; Iiritano, S; Capula, C; Arcidiacono, B; Nocera, A; Possidente, K; Baudi, F; Ventura, V; Brunetti, G; Brunetti, Fs; Vero, R; Maio, R; Hodoglugil, U; Durlach, V; Pullinger, Cr; Goldfine, Id; Foti, D; Pavia, M; Greco, M; Brunetti, A; Perticone, F; Sciacqua, A
A polymorphism of HMGA1 protects against proliferative diabetic retinopathy by impairing HMGA1-induced VEGFA expression 1-gen-2016 Chiefari, E; Ventura, V; Capula, C; Randazzo, G; Scorcia, V; Fedele, M; Arcidiacono, B; Nevolo, Mt; Bilotta, Fl; Vitiello, M; Palmieri, C; Gulletta, E; Fusco, A; Foti, D; Vero, R; Brunetti, A