Sfoglia per Autore
Ghrelin and adiponectin in patients with Cushing's disease before and after successful transsphenoidal surgery
2005 R. Libè, P.S. Morpurgo, V. Cappiello, A. Maffini, S. Bondioni, M. Locatelli, M. Zavanone, P. Beck-Peccoz, A. Spada
The limited role of midnight salivary cortisol levels in the diagnosis of subclinical hypercortisolism in patients with adrenal incidentaloma
2009 B. Masserini, V. Morelli, S. Bergamaschi, F. Ermetici, C. Eller-Vainicher, A.M. Barbieri, M.A. Maffini, A. Scillitani, B. Ambrosi, P. Beck Peccoz, I. Chiodini
Serum BAFF concentrations in patients with Graves' disease and orbitopathy before and after immunosuppressive therapy
2012 G. Vannucchi, D. Covelli, N. Currò, D. Dazzi, A. Maffini, I. Campi, P. Bonara, C. Guastella, L. Pignataro, R. Ratiglia, P. Beck Peccoz, M. Salvi
The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defects
2014 M. Muzza, S. Rabbiosi, M.C. Vigone, I. Zamproni, V. Cirello, M.A. Maffini, K. Maruca, N. Schoenmakers, L. Beccaria, F. Gallo, S.M. Park, P. Beck-Peccoz, L. Persani, G. Weber, L. Fugazzola
Fetal cell microchimerism in papillary thyroid cancer : a role in the outcome of the disease
2015 V. Cirello, C. Colombo, M. Perrino, S. De Leo, M. Muzza, M.A. Maffini, L. Fugazzola
Retinal photoreceptor functions are compromised in patients with resistance to thyroid hormone syndrome (RTHβ)
2017 I. Campi, G. Cammarata, S. Bianchi Marzoli, P. Beck-Peccoz, D. Santarsiero, D. Dazzi, A. Bottari de Castello, E.G. Taroni, F. Viola, C. Mian, S. Watuntantrige Fernando, C. Pelusi, M. Muzza, M.A. Maffini, L. Persani
Association of GNAS Imprinting Defects and Deletions of Chromosome 2 in Two Patients : Clues Explaining Phenotypic Heterogeneity in Pseudohypoparathyroidism Type 1B/iPPSD3
2019 F.M. Elli, L. Desanctis, M.A. Maffini, P. Bordogna, D. Tessaris, A. Pirelli, M. Arosio, A. Linglart, G. Mantovani
2q37 Deletions in Patients With an Albright Hereditary Osteodystrophy Phenotype and PTH Resistance
2019 F.M. Elli, L. de Sanctis, B. Madeo, M.A. Maffini, P. Bordogna, A. Pirelli, M. Arosio, G. Mantovani
Improved Molecular Diagnosis of McCune-Albright Syndrome and Bone Fibrous Dysplasia by Digital PCR
2019 F.M. Elli, L. de Sanctis, M. Bergallo, M.A. Maffini, A. Pirelli, I. Galliano, P. Bordogna, M. Arosio, G. Mantovani
Case Report: A Novel ARMC5 Germline Mutation in a Patient with Primary Bilateral Macronodular Adrenal Hyperplasia and Hypogammaglobulinemia
2022 W. Vena, V. Morelli, M. Carrabba, F. Elli, G. Fabio, I. Muller, C. Lucca, M.A. Maffini, A.G. Lania, G. Mantovani, M. Arosio
Targeted silencing of GNAS in a human model of osteoprogenitor cells results in the deregulation of the osteogenic differentiation program
2024 F.M. Elli, D. Mattinzoli, M. Ikehata, F. Bagnaresi, M.A. Maffini, G. Del Sindaco, A. Pagnano, C. Lucca, P. Messa, M. Arosio, G. Castellano, C.M. Alfieri, G. Mantovani
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