MANTOVANI, GIOVANNA
MANTOVANI, GIOVANNA
Dipartimento di Scienze Cliniche e di Comunità
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
A Case Report of Severe Hypotonic Hyponatremia Secondary to Concomitant Intake of Desmopressin Replacement Therapy and Non-Steroidal Anti-Inflammatory Drugs
2012 E. Ferrante, E. Verrua, G. Mantovani, A. Noto, E. Sala, E. Malchiodi, G. Iapichino, P. Beck-Peccoz, A. Spada
A novel mechanism regulating dopamine receptor type 2 (DRD2) signal transduction in pituitary tumoral cells: the role of cAMP/PKA-induced filamin A (FLNA) phosphorylation
2021 F. Mangili, D. Treppiedi, R. Catalano, G. Marra, G. DI MURO, A. Spada, M. Arosio, E.M. Peverelli, G. Mantovani
A novel pathway activated by somatostatin receptor type 2 (SST2): Inhibition of pituitary tumor cell migration and invasion through cytoskeleton protein recruitment
2018 E. Peverelli, E. Giardino, D. Treppiedi, R. Catalano, F. Mangili, M. Locatelli, A.G. Lania, M. Arosio, A. Spada, G. Mantovani
A Rare SPRY4 Gene Mutation Is Associated With Anosmia and Adult-Onset Isolated Hypogonadotropic Hypogonadism
2019 R. Indirli, B. Cangiano, E. Profka, G. Mantovani, L. Persani, M. Arosio, M. Bonomi, E. Ferrante
A Severe Inactivating PTH/PTHrP Signaling Disorder Type 2 in a Patient Carrying a Novel Large Deletion of the GNAS Gene : A Case Report and Review of the Literature
2020 A. Brancatella, G. Mantovani, F.M. Elli, S. Borsari, C. Marcocci, F. Cetani
Absence of thyroid transcription factor-1 expression in human parathyroid and pituitary glands
2001 G. Mantovani, S. Corbetta, R. Romoli, L. Alberti, P. Beck-Peccoz, A. Spada
Activation of the dopamine receptor type-2 (DRD2) promoter by 9-cis retinoic acid in a cellular model of cushing's disease mediates the inhibition of cell proliferation and ACTH secretion without a complete corticotroph-to-melanotroph transdifferentiation
2014 G. Occhi, D. Regazzo, N.M. Albiger, F. Ceccato, S. Ferasin, M. Scanarini, L. Denaro, C. Cosma, M. Plebani, M.F. Cassarino, G. Mantovani, G.K. Stalla, F. Pecori Giraldi, M. Paez Pareda, C. Scaroni
Activity and function of the nuclear factor kappaB pathway in human parathyroid tumors
2005 S. Corbetta, L. Vicentini, S. Ferrero, A. Lania, G. Mantovani, D. Cordella, P. Beck-Peccoz, A. Spada
Adiponectin expression in human fetal tissues during mid- and late gestation
2005 S.L. Corbetta, G.P. Bulfamante, D. Cortelazzi, V. Barresi, I. Cetin, G. Mantovani, S. Bondioni, P.L.M. Beck-Peccoz, A. Spada
Adrenal insufficiency at the time of COVID-19: a retrospective study in patients referring to a tertiary centre
2021 G. Carosi, V. Morelli, G. Del Sindaco, A.L. Serban, A. Cremaschi, S. Frigerio, G. Rodari, E. Profka, R. Indirli, R. Mungari, V. Resi, E. Orsi, E. Ferrante, A. Dolci, C. Giavoli, M. Arosio, G. Mantovani
Albright Hereditary Osteodystrophy and Pseudohypoparathyroidism Type
2014 G. Mantovani, F. Elli
An alternate translation initiation site circumvents an amino-terminal DAX1 nonsense mutation leading to a mild form of X-linked adrenal hypoplasia congenita
2003 G. Ozisik, G. Mantovani, J.C. Achermann, L. Persani, A. Spada, J. Weiss, P. Beck-Peccoz, J.L. Jameson
Analysis of genetic variants of phosphodiesterase 11A (PDE11A) in acromegalic patients
2009 E. Peverelli, F. Ermetici, M. Filopanti, F. Elli, C. Ronchi, G. Mantovani, S. Ferrero, S. Bosari, P. Beck-Peccoz, A. Lania, A. Spada
Analysis of GNAS1 and PRKAR1A gene mutations in human cardiac myxomas not associated with multiple endocrine disorders
2009 G. Mantovani, S. Bondioni, S. Corbetta, L. Menicanti, B. Rubino, E. Peverelli, P. Labarile, C. Dall'Asta, B. Ambrosi, P. Beck Peccoz, A.G. Lania, A. Spada
Approach to hyponatremia according to the clinical setting: Consensus statement from the Italian Society of Endocrinology (SIE), Italian Society of Nephrology (SIN), and Italian Association of Medical Oncology (AIOM)
2018 E. Sbardella, A..M. Isidori, G. Arnaldi, M. Arosio, C. Barone, A. Benso, R. Berardi, G. Capasso, M. Caprio, F. Ceccato, G. Corona, S. della Casa, L. de Nicola, M. Faustini-Fustini, E. Fiaccadori, L. Gesualdo, S. Gori, A. Lania, G. Mantovani, P. Menã, G. Parenti, C. Pinto, R. Pivonello, P. Razzore, G. Regolisti, C. Scaroni, F. Trepiccione, A. Lenzi, A. Peri
Arterial Embolization and Second-Look in Spindle Cell Oncocytoma of the Pituitary Gland : Case Report and Review of Literature
2020 L. Tariciotti, A. Arrichiello, G. Fiore, G.A. Bertani, G. Conte, A. Paolucci, E. Ferrante, G. Mantovani, M. Locatelli
Arthropathy in acromegaly : a questionnaire-based estimation of motor disability and its relation with quality of life and work productivity
2019 L.M. Fatti, B. Cangiano, G. Vitale, L. Persani, G. Mantovani, E. Sala, M. Arosio, P. Maffei, F. Dassie, M. Mormando, A. Giampietro, L. Tanda, E.R. Masiello, E. Nazzari, D. Ferone, S. Corbetta, E. Passeri, F. Guaraldi, S. Grottoli, S. Cannavo, M.L.T. Torre, D. Soranna, A. Zambon, F. Cavagnini, M. Scacchi
Assessing the presence of abnormal regulation of cortisol secretion by membrane hormone receptors : in vivo and in vitro studies in patients with functioning and non-functioning adrenal adenoma
2004 C.G. Dall'Asta, E. Ballarè, G. Mantovani, B.E. Ambrosi, A. Spada, L. Barbetta, P. Colombo, P. Travaglini, P. Loli, P.L.M. Beck-Peccoz
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