VIGONE, MARIA CRISTINA EUGENIA
VIGONE, MARIA CRISTINA EUGENIA
Universita' degli Studi di MILANO
Congenital hypothyroidism with gland in situ: diagnostic re-evaluation
2005 G. Weber, M.C. Vigone, A. Passoni, M. Odoni, P.L. Paesano, F. Dosio, M.C. Proverbio, C. Corbetta, L. Persani, G. Chiumello
Congenital hypothyroidism: a 2020 consensus guidelines update An ENDO-EUROPEAN REFERENCE NETWORK (ERN) initiative endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology
2020 A.S. van Trotsenburg, A. Stoupa, J. Léger, T.R. Rohrer, C. Peters, L. Fugazzola, A. Cassio, C. Heinrichs, V. Beauloye, J. Pohlenz, P. Rodien, R. Coutant, G. Szinnai, P. Murray, B. Bartès, D. Luton, M. Salerno, L. De Sanctis, M.C. Vigone, H. Krude, L. Persani, M. Polak
Evolution of thyroid function in preterm infants detected by screening for congenital hypothyroidism
2014 M.C. Vigone, S. Caiulo, M. Di Frenna, S. Ghirardello, C. Corbetta, F. Mosca, G. Weber
Frequent TSH Receptor Genetic Alterations with Variable Signaling Impairment in a Large Series of Children with Nonautoimmune Isolated Hyperthyrotropinemia
2012 D. Calebiro, G. Gelmini, D. Cordella, M. Bonomi, F. Winkler, H. Biebermann, A. De Marco, F. Marelli, D.V. Libri, F. Antonica, M.C. Vigone, M. Cappa, C. Mian, A. Sartorio, P. Beck Peccoz, G. Radetti, G. Weber, L. Persani
Neonatal Screening for Congenital Hypothyroidism: What Can We Learn from Discordant Twins
2019 E. Medda, M.C. Vigone, A. Cassio, F. Calaciura, P. Costa, G. Weber, T. De Filippis, G. Gelmini, M. Di Frenna, S. Caiulo, R. Ortolano, D. Rotondi, M. Bartolucci, R. Gelsomino, S. De Angelis, M. Gabbianelli, L. Persani, A. Olivieri
Thyroid scintigraphy and perchlorate test after recombinant human TSH: a new tool for the differential diagnosis of congenital hypothyroidism during infancy
2007 L. Fugazzola, L. Persani, G. Vannucchi, M. Carletto, D. Mannavola, M.C. Vigone, F. Cortinovis, L. Beccaria, V. Longari,G. Weber, P. Beck-Peccoz