Последние публикации
Treatment of congenital hypothyroidism: comparison between L-thyroxine oral solution and tablet formulations up to 3 years of age
(2021) European journal of endocrinology, 186 (1), pp. 45-52. DOI: 10.1530/EJE-20-1444
Vigone, M.C., Ortolano, R., Vincenzi, G., Pozzi, C., Ratti, M., Assirelli, V., Vissani, S., Cavarzere, P., Mussa, A., Gastaldi, R., Di Mase, R., Salerno, M., Street, M.E., Trombatore, J., Weber, G., Cassio, A.
Thyroid nodular disease and PTEN mutation in a multicentre series of children with PTEN hamartoma tumor syndrome (PHTS)
(2021) Endocrine, 74 (3), pp. 632-637. DOI: 10.1007/s12020-021-02805-y
Tuli, G., Munarin, J., Mussa, A., Carli, D., Gastaldi, R., Borgia, P., Vigone, M.C., Abbate, M., Ferrero, G.B., De Sanctis, L.
Congenital Hypothyroidism: A 2020-2021 Consensus Guidelines Update - An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology
(2021) Thyroid, 31 (3), pp. 387-419. DOI: 10.1089/thy.2020.0333
Van Trotsenburg, P., Stoupa, A., Léger, J., Rohrer, T., Peters, C., Fugazzola, L., Cassio, A., Heinrichs, C., Beauloye, V., Pohlenz, J., Rodien, P., Coutant, R., Szinnai, G., Murray, P., Bartés, B., Luton, D., Salerno, M., De Sanctis, L., Vigone, M., Krude, H., Persani, L., Polak, M.
Newborn screening for congenital hypothyroidism: The benefit of using differential TSH cutoffs in a 2-screen program
(2021) Journal of Clinical Endocrinology and Metabolism, 106 (1), pp. E338-E349. DOI: 10.1210/clinem/dgaa789
Caiulo, S., Corbetta, C., Di Frenna, M., Medda, E., De Angelis, S., Rotondi, D., Vincenzi, G., De Filippis, T., Patricelli, M.G., Persani, L., Barera, G., Weber, G., Olivieri, A., Vigone, M.C.
Block-and-replace” treatment in Graves’ disease: experience in a cohort of pediatric patients
(2020) Journal of Endocrinological Investigation, 43 (5), pp. 595-600. DOI: 10.1007/s40618-019-01144-0
Vigone, M.C., Peroni, E., Di Frenna, M., Mora, S., Barera, G., Weber, G.
Neonatal Screening for Congenital Hypothyroidism: What Can We Learn from Discordant Twins
(2019) Journal of Clinical Endocrinology and Metabolism, 104 (12), pp. 5765-5779. DOI: 10.1210/jc.2019-00900
Medda, E., Vigone, M.C., Cassio, A., Calaciura, F., Costa, P., Weber, G., De Filippis, T., Gelmini, G., Di Frenna, M., Caiulo, S., Ortolano, R., Rotondi, D., Bartolucci, M., Gelsomino, R., De Angelis, S., Gabbianelli, M., Persani, L., Olivieri, A.
Influence of Hashimoto thyroiditis on the development of thyroid nodules and cancer in children and adolescents
(2019) Journal of the Endocrine Society, 3 (3), pp. 607-616. DOI: 10.1210/js.2018-00287
Radetti, G., Loche, S., D'Antonio, V., Salerno, M., Guzzetti, C., Aversa, T., Cassio, A., Cappa, M., Gastaldi, R., Deluca, F., Vigone, M.C., Tronconi, G.M., Corrias, A.
Mild TSH resistance: Clinical and hormonal features in childhood and adulthood
(2017) Clinical Endocrinology, 87 (5), pp. 587-596. DOI: 10.1111/cen.13387
Vigone, M.C., Di Frenna, M., Guizzardi, F., Gelmini, G., de Filippis, T., Mora, S., Caiulo, S., Sonnino, M., Bonomi, M., Persani, L., Weber, G.
Ardissino, D., Weber, G., Gentilini, D., Guizzardi, F., Duga, S., Persani, L. A frequent oligogenic involvement in congenital hypothyroidism
(2017) Human Molecular Genetics, 26 (13), pp. 2507-2514. Cited 78 times. DOI: 10.1093/hmg/ddx145
De Filippis, T., Gelmini, G., Paraboschi, E., Vigone, M.C., Frenna, M.D., Marelli, F., Bonomi, M., Cassio, A., Larizza, D., Moro, M., Radetti, G., Salerno, M.,
Evolution of thyroid function in preterm infants detected by screening for congenital hypothyroidism
(2014) Journal of Pediatrics, 164 (6), pp. 1296-1302. Cited 63 times. DOI: 10.1016/j.jpeds.2013.12.048
Vigone, M.C., Caiulo, S., Di Frenna, M., Ghirardello, S., Corbetta, C., Mosca, F., Weber, G.
Congenital hypothyroidism treatment in infants: A comparative study between liquid and tablet formulations of levothyroxine
(2014) Hormone Research in Paediatrics, 81 (1), pp. 50-54. Cited 41 times. DOI: 10.1159/000356047
Peroni, E., Vigone, M.C., Mora, S., Bassi, L.A., Pozzi, C., Passoni, A., Weber, G.
The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defects
(2014) Journal of Clinical Endocrinology and Metabolism, 99 (3), pp. E544-E553. Cited 57 times. DOI: 10.1210/jc.2013-3618
Muzza, M., Rabbiosi, S., Vigone, M.C., Zamproni, I., Cirello, V., Maffini, M.A., Maruca, K., Schoenmakers, N., Beccaria, L., Gallo, F., Park, S.-M., Beck-Peccoz, P., Persani, L., Weber, G., Fugazzola, L.
Congenital hypothyroidism with eutopic thyroid gland: Analysis of clinical and biochemical features at diagnosis and after re-evaluation
(2013) Journal of Clinical Endocrinology and Metabolism, 98 (4), pp. 1395-1402. DOI: 10.1210/jc.2012-3174
Rabbiosi, S., Vigone, M.C., Cortinovis, F., Zamproni, I., Fugazzola, L., Persani, L., Corbetta, C., Chiumello, G., Weber, G.
Surgical management of pediatric Graves' disease: An effective definitive treatment
(2012) Pediatric Surgery International, 28 (6), pp. 609-614. DOI: 10.1007/s00383-012-3095-5
Peroni, E., Angiolini, M.R., Vigone, M.C., Mari, G., Chiumello, G., Beretta, E., Weber, G.
A 7-year experience with low blood TSH cutoff levels for neonatal screening reveals an unsuspected frequency of congenital hypothyroidism (CH)
(2009) Clinical Endocrinology, 71 (5), pp. 739-745. DOI: 10.1111/j.1365-2265.2009.03568.x
Corbetta, C., Weber, G., Cortinovis, F., Calebiro, D., Passoni, A., Vigone, M.C., Beck-Peccoz, P., Chiumello, G., Persani, L.
