European thyroid journal: passing on the baton

por Pearce, S H S, Persani, L
Publicado 2023

Switch to restoration therapy in a testosterone treated central hypogonadism with erythrocytosis

por Cangiano, B, Cacciatore, C, Persani, L, Bonomi, M
Publicado 2017

Non-autoimmune hyperthyroidism caused by thyroid-stimulating hormone receptor germline mutations - 2012 European Thyroid Association Guidelines

por Paschke, R, Niedziela, M, Vaidya, B, Persani, L, Rapoport, B, Leclere, J
Publicado 2013

Long-term effects of somatostatin analogues in rat GH-secreting pituitary tumor cell lines

por Dicitore, A., Saronni, D., Gaudenzi, G., Carra, S., Cantone, M. C., Borghi, M. O., Persani, L., Vitale, G.
Publicado 2021

Predictors of reproductive and non-reproductive outcomes of gonadotropin mediated pubertal induction in male patients with congenital hypogonadotropic hypogonadism (CHH)

por Cangiano, B., Goggi, G., Federici, S., Bresesti, C., Cotellessa, L., Guizzardi, F., Vezzoli, V., Duminuco, P., Persani, L., Bonomi, M.
Publicado 2021

Basal and stimulated calcitonin for the diagnosis of medullary thyroid cancer: updated thresholds and safety assessment

por Fugazzola, L., Di Stefano, M., Censi, S., Repaci, A., Colombo, C., Grimaldi, F., Magri, F., Pagotto, U., Iacobone, M., Persani, L., Mian, C.
Publicado 2020

High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian function

por Bestetti, I, Castronovo, C, Sironi, A, Caslini, C, Sala, C, Rossetti, R, Crippa, M, Ferrari, I, Pistocchi, A, Toniolo, D, Persani, L, Marozzi, A, Finelli, P
Publicado 2019

Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidism

por Gentilini, D., Muzza, M., de Filippis, T., Vigone, M. C., Weber, G., Calzari, L., Cassio, A., Di Frenna, M., Bartolucci, M., Grassi, E. S., Carbone, E., Olivieri, A., Persani, L.
Publicado 2022

The physiological sonographic features of the ovary in healthy subjects: a joint systematic review and meta-analysis by the Italian Society of Gynecology and Obstetrics (SIGO) and...

por Moro, F., Scavello, I., Maseroli, E., Rastrelli, G., Baima Poma, C., Bonin, C., Dassie, F., Federici, S., Fiengo, S., Guccione, L., Villani, M., Gambineri, A., Mioni, R., Moghetti, P., Moretti, C., Persani, L., Scambia, G., Giorgino, F., Vignozzi, L.
Publicado 2022

IGSF1 Deficiency: Lessons From an Extensive Case Series and Recommendations for Clinical Management

por Joustra, S. D., Heinen, C. A., Schoenmakers, N., Bonomi, M., Ballieux, B. E. P. B., Turgeon, M.-O., Bernard, D. J., Fliers, E., van Trotsenburg, A. S. P., Losekoot, M., Persani, L., Wit, J. M., Biermasz, N. R., Pereira, A. M., Oostdijk, W.
Publicado 2016

The current landscape of European registries for rare endocrine conditions

por Ali, S R, Bryce, J, Cools, M, Korbonits, M, Beun, J G, Taruscio, D, Danne, T, Dattani, M, Dekkers, O M, Linglart, A, Netchine, I, Nordenstrom, A, Patocs, A, Persani, L, Reisch, N, Smyth, A, Sumnik, Z, Visser, W E, Hiort, O, Pereira, A M, Ahmed, S F
Publicado 2018

Electronic reporting of rare endocrine conditions within a clinical network: results from the EuRRECa project

por Ali, S R, Bryce, J, Priego-Zurita, A L, Cherenko, M, Smythe, C, de Rooij, T M, Cools, M, Danne, T, Katugampola, H, Dekkers, O M, Hiort, O, Linglart, A, Netchine, I, Nordenstrom, A, Attila, P, Persani, L, Reisch, N, Smyth, A, Sumnik, Z, Taruscio, D, Visser, W E, Pereira, A M, Appelman-Dijkstra, N M, Ahmed, S F
Publicado 2023