CHIEFARI, EUSEBIO DOMENICO ANDREA FERNANDO
CHIEFARI, EUSEBIO DOMENICO ANDREA FERNANDO
Dipartimento di Scienze della Salute
A case of metastatic medullary thyroid carcinoma: early identification before surgery of a ret proto-oncogene somatic mutation in fine needle aspirate specimen
1997-01-01 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
1997-01-01 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
1997-01-01 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
2001-01-01 E., Chiefari; R., Chiarella; B., Tardio; Arturi, F; V., Trischitta; S., Filetti; M., Zingrillo; Russo, D.
A modified quantitative EMSA and its application in the study of RNA-protein interactions
2008-01-01 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
2016-01-01 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
2015-01-01 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
2000-01-01 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
2000-01-01 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
2000-01-01 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
2003-01-01 Foti, D.; Iuliano, R; Chiefari, E.; Brunetti, A.
A nucleoprotein complex containing Sp1, C/EBPb, and HMGI(Y) controls human insulin receptor gene transcription
2003-01-01 Foti, D.; Iuliano, R; Chiefari, E; Brunetti, A
A Partial Phenotype of adFNDI Related to the Signal Peptide c.55G>A Variant of the AVP Gene
2021-01-01 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
2000-01-01 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
2000-01-01 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
2013-01-01 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
2016-01-01 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
A thyroid follicular cancer presenting as a hot nodule and hyperfunctioning because of an activating mutation of the TSH receptor
1996-01-01 Russo, D.; Belfiore, A.; Tumino, S.; Arturi, F; Pontecorvi, A.; Chiefari, E.; Grasso, G.; Pezzino, V.; Filetti, S.
A Val 677 activating mutation of the Thyrotropin receptor in a Hürthle cell thyroid carcinoma associated with thyrotoxicosis
1999-01-01 Russo, D.; Wong, Mg; Costante, G; Chiefari, E; Treseler, Pa
A Val677 activating mutation of the thyrotropin receptor in a Hurtle cell thyroid carcinoma associated with thyrotossicosis
1999-01-01 Russo, D.; Wong, M. G.; Costante, G.; Chiefari, E.; Treseler, P. A.; Arturi, F; Filetti, S.; Clark, O. H.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
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 | E., Chiefari; R., Chiarella; B., Tardio; Arturi, F; V., Trischitta; S., Filetti; M., Zingrillo; 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/EBPb, and HMGI(Y) controls human insulin receptor gene transcription | 1-gen-2003 | Foti, D.; Iuliano, R; Chiefari, E; 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 | |
A thyroid follicular cancer presenting as a hot nodule and hyperfunctioning because of an activating mutation of the TSH receptor | 1-gen-1996 | Russo, D.; Belfiore, A.; Tumino, S.; Arturi, F; Pontecorvi, A.; Chiefari, E.; Grasso, G.; Pezzino, V.; Filetti, S. | |
A Val 677 activating mutation of the Thyrotropin receptor in a Hürthle cell thyroid carcinoma associated with thyrotoxicosis | 1-gen-1999 | Russo, D.; Wong, Mg; Costante, G; Chiefari, E; Treseler, Pa | |
A Val677 activating mutation of the thyrotropin receptor in a Hurtle cell thyroid carcinoma associated with thyrotossicosis | 1-gen-1999 | Russo, D.; Wong, M. G.; Costante, G.; Chiefari, E.; Treseler, P. A.; Arturi, F; Filetti, S.; Clark, O. H. |