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Journal of Endocrinological Investigation|August 11, 2023
COVID-19 lockdown and the rate of central precocious pubertyG Goggi, M Moro, A Chilà, et al.Journal of Hepatology|May 1, 1992
Hepatitis C virus testing in primary biliary cirrhosisE Bertolini, P M Battezzati, P Zermiani, et al.The Journal of Clinical Endocrinology and Metabolism|December 17, 1997
Resistance to thyrotropin (TSH) in three families is not associated with mutations in the TSH receptor or TSHJ Xie, S Pannain, J Pohlenz, et al.Journal of Endocrinological Investigation|January 6, 2018
A balanced reciprocal translocation t(10;15)(q22.3;q26.1) interrupting ACAN gene in a family with proportionate short statureM Crippa, S Giangiobbe, R Villa, et al.Human Reproduction (Oxford, England)|January 29, 2019
High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian functionI Bestetti, C Castronovo, A Sironi, et al.Clinical and Experimental Immunology|June 10, 2010
Rituximab treatment in patients with active Graves' orbitopathy: effects on proinflammatory and humoral immune reactionsG Vannucchi, I Campi, M Bonomi, et al.Journal of Endocrinological Investigation|January 4, 2021
Hidden hypercortisolism: a too frequently neglected clinical conditionL Giovanelli, C Aresta, V Favero, et al.Journal of Endocrinological Investigation|September 7, 2022
Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidismD Gentilini, M Muzza, T de Filippis, et al.The Journal of Clinical Endocrinology and Metabolism|January 16, 2014
The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defectsM Muzza, S Rabbiosi, M C Vigone, et al.Panminerva Medica|October 8, 2014
A clinical research integration special program (CRISP) for young women with primary ovarian insufficiencyA Falorni, V Minarelli, C M Eads, et al.Pageof 11