Genetics of primary ovarian insufficiency von Rossetti, R., Ferrari, I., Bonomi, M., Persani, L.

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Role of Jagged1-Notch pathway in thyroid development von Marelli, F., Persani, L.

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

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Thyroid gland development and function in the zebrafish model von Porazzi, P., Calebiro, D., Benato, F., Tiso, N., Persani, L.

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

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European thyroid journal: passing on the baton von Pearce, S H S, Persani, L

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Predictors of reproductive and non-reproductive outcomes of gonadotropin mediated pubertal induction in male patients with congenital hypogonadotropic hypogonadism (CHH) von Cangiano, B., Goggi, G., Federici, S., Bresesti, C., Cotellessa, L., Guizzardi, F., Vezzoli, V., Duminuco, P., Persani, L., Bonomi, M.

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Basal and stimulated calcitonin for the diagnosis of medullary thyroid cancer: updated thresholds and safety assessment von Fugazzola, L., Di Stefano, M., Censi, S., Repaci, A., Colombo, C., Grimaldi, F., Magri, F., Pagotto, U., Iacobone, M., Persani, L., Mian, C.

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ACROMORFO study: gait analysis in a cohort of acromegalic patients von Cimolin, V., Premoli, C., Bernardelli, G., Amenta, E., Galli, M., Donno, L., Lucini, D., Fatti, L. M., Cangiano, B., Persani, L., Vitale, G.

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Long-term effects of somatostatin analogues in rat GH-secreting pituitary tumor cell lines von Dicitore, A., Saronni, D., Gaudenzi, G., Carra, S., Cantone, M. C., Borghi, M. O., Persani, L., Vitale, G.

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Hidden hypercortisolism: a too frequently neglected clinical condition von Giovanelli, L., Aresta, C., Favero, V., Bonomi, M., Cangiano, B., Eller-Vainicher, C., Grassi, G., Morelli, V., Pugliese, F., Falchetti, A., Gennari, L., Scillitani, A., Persani, L., Chiodini, I.

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COVID-19 lockdown and the rate of central precocious puberty von Goggi, G., Moro, M., Chilà, A., Fatti, L., Cangiano, B., Federici, S., Galazzi, E., Carbone, E., Soranna, D., Vezzoli, V., Persani, L., Bonomi, M.

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Body weight variation is not an independent factor in the determination of functional hypothalamic amenorrhea in anorexia nervosa von Cacciatore, C., Cangiano, B., Carbone, E., Spagnoli, S., Cid Ramirez, M. P., Polli, N., Bonomi, M., Persani, L.

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The Clinical and Molecular Characterization of Patients With Dyshormonogenic Congenital Hypothyroidism Reveals Specific Diagnostic Clues for DUOX2 Defects von 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

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

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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... von 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.

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The current landscape of European registries for rare endocrine conditions von 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

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The IGSF1 Deficiency Syndrome: Characteristics of Male and Female Patients von Joustra, S. D, Schoenmakers, N, Persani, L, Campi, I, Bonomi, M, Radetti, G, Beck-Peccoz, P, Zhu, H, Davis, T. M. E, Sun, Y, Corssmit, E. P, Appelman-Dijkstra, N. M, Heinen, C. A, Pereira, A. M, Varewijck, A. J, Janssen, J. A. M. J. L, Endert, E, Hennekam, R. C, Lombardi, M. P, Mannens, M. M. A. M, Bak, B, Bernard, D. J, Breuning, M. H, Chatterjee, K, Dattani, M. T, Oostdijk, W, Biermasz, N. R, Wit, J. M, van Trotsenburg, A. S. P

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Two novel truncating variants of the AAAS gene causative of the triple A syndrome von Vezzoli, V., Duminuco, P., Pogliaghi, G., Saccone, M., Cangiano, B., Rosatelli, M. C., Meloni, A., Persani, L., Bonomi, M.

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Arthropathy in acromegaly: a questionnaire-based estimation of motor disability and its relation with quality of life and work productivity von Fatti, L. M., Cangiano, B., Vitale, G., Persani, L., Mantovani, G., Sala, E., Arosio, M., Maffei, P., Dassie, F., Mormando, M., Giampietro, A., Tanda, L., Masiello, E. R., Nazzari, E., Ferone, D., Corbetta, S., Passeri, E., Guaraldi, F., Grottoli, S., Cannavò, S., Torre, M. L. T., Soranna, D., Zambon, A., Cavagnini, F., Scacchi, M.

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