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BORSARI, SIMONA Statistiche

BORSARI, SIMONA  

DIPARTIMENTO DI MEDICINA CLINICA E SPERIMENTALE  

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Titolo Data di pubblicazione Autore(i) File
A New MEN2 Syndrome with Clinical Features of Both MEN2A and MEN2B Associated with a New RET Germline Deletion 1-gen-2020 Giani, C.; Ramone, T.; Romei, C.; Ciampi, R.; Tacito, A.; Valerio, L.; Agate, L.; Ugolini, C.; Marino, M.; Basolo, F.; Franchi, A.; Borsari, S.; Michelucci, A.; Selli, C.; Materazzi, G.; Cetani, F.; Elisei, R.
A Novel Mutation in the Calcium Sensing Receptor Gene in an Italian Family Affected by Autosomal Dominant Hypocalcemia 1-gen-2018 Cetani, F; Borsari, S; Saponaro, F; Pardi, E; Banti, C; Mazoni, L; Apicella, M; Marcocci, C
A Prospective Study on Juvenile Primary Hyperparathyroidism Population. 1-gen-2014 Saponaro, F; Cacciato, F; Pardi, E; Borsari, S; Marcocci, C; Cetani, F
A reappraisal of the Rb1 gene abnormalities in the diagnosis of parathyroid cancer 1-gen-2004 Cetani, F; Pardi, E; Viacava, P; Pollina, Gd; Fanelli, G; Picone, Angelo; Borsari, Simona; Gazzerro, E; Miccoli, Paolo; Berti, Piero; Pinchera, A; Marcocci, Claudio
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 1-gen-2020 Brancatella, A.; Mantovani, G.; Elli, F. M.; Borsari, S.; Marcocci, C.; Cetani, F.
Beta-catenin activation is not involved in sporadic parathyroid carcinomas and adenomas 1-gen-2010 Cetani, F; Pardi, E; Banti, C; Collecchi, P; Viacava, P; Borsari, S; Fanelli, G; Naccarato, Ag; Saponaro, F; Berti, P; Miccoli, P; Pinchera, A; Marcocci, C
CDC73 mutational status and loss of parafibromin in the outcome of parathyroid cancer. 1-gen-2013 Cetani, F; Banti, C; Pardi, E; Borsari, S; Viacava, P; Miccoli, P; Torregrossa, L; Basolo, F; Pelizzo, Mr; Rugge, M; Pennelli, G; Gasparri, G; Papotti, M; Volante, M; Vignali, E; Saponaro, F; Marcocci, C
CDC73/HRPT2 mutations and parafibromin immunohistochemistry in a large series of sporadic parathyroid carcinomas and atypical adenomas 1-gen-2013 Cetani, F; Banti, C; Pardi, E; Torregrossa, L; Borsari, S; Saponaro, F; Rugge, M; Pennelli, G; Pelizzo, M; Papotti, M; Volante, M; Gasparri, G; Miccoli, P; Marcocci, C
Clinical profile of juvenile primary hyperparathyroidism: a prospective study 1-gen-2018 Saponaro, Federica; Marcocci, Claudio; Cacciatore, Federica; Miccoli, Mario; Pardi, Elena; Borsari, Simona; Materazzi, Gabriele; Miccoli, Paolo; Cetani, Filomena
Correction to: Whole exome sequencing in familial isolated primary hyperparathyroidism 1-gen-2020 Cetani, F; Pardi, E; Aretini, P; Saponaro, F; Borsari, S; Mazoni, L; Apicella, M; Civita, P; La Ferla, M; Caligo, M A; Lessi, F; Mazzanti, C M; Torregrossa, L; Oppo, A; Marcocci, C
Different somatic alterations of the HRPT2 gene in a patient with recurrent sporadic primary hyperparathyroidism carrying an HRPT2 germline mutation 1-gen-2007 Cetani, F; Pardi, E; Ambrogini, E; Viacava, P; Borsari, Simona; LEMMI GIGLI, Mauro; Cianferotti, Luisella; Miccoli, Paolo; Pinchera, Aldo; Arnold, A; Marcocci, Claudio
Do Patients with Atypical Parathyroid Adenoma Need Close Follow-up? 1-gen-2021 Saponaro, F.; Pardi, E.; Mazoni, L.; Borsari, S.; Torregrossa, L.; Apicella, M.; Frustaci, G.; Materazzi, G.; Miccoli, P.; Basolo, F.; Marcocci, C.; Cetani, F.
Exome analysis of a large family with Familial Isolated Primary Hyperparathyroidism (FIHP) and multiple cancers. 1-gen-2017 Cetani, F; Pardi, E; Borsari, S; Saponaro, F; Torregrossa, L; Mazzanti, C; Aretini, P; La Ferla, M; Franceschi, S; Lessi, F; Civita, P; Marcocci, C
Familial and Hereditary Forms of Primary Hyperparathyroidism 1-gen-2018 Cetani, F.; Saponaro, F.; Borsari, S.; Marcocci, C.
Familial hypocalciuric hypercalcemia associated with a novel homozygous loss-of-function mutation, E671D, of the calcium-sensing receptor gene 1-gen-2014 Cetani, F; Borsari, S; Pardi, E; Bagattini, B; Saponaro, F; Marcocci, C
Familial hypocalciuric hypercalcemia type 1 due to a novel homozygous mutation of the calcium-sensing receptor gene 1-gen-2017 Borsari, Simona; Marcocci, Claudio; Cetani, F.
Fenotipo misto MEN2A/MEN2B da nuova mutazione germinale di RET: prima descrizione clinico-genetica e iconografia 1-gen-2020 Giani, Carlotta; Ramone, Teresa; Romei, Cristina; Ciampi, Raffaele; Valerio, Laura; Tacito, Alessia; Agate, Laura; Ugolini, Clara; Marinò, Michele; Basolo, Fulvio; Franchi, Alessandro; Borsari, Simona; Michelucci, Angela; Selli, Cesare; Materazzi, Gabriele; Cetani, Filomena; Elisei, Rossella
Functional characterization of a CDKN1B mutation in a Sardinian kindred with multiple endocrine neoplasia type 4 (MEN4) 1-gen-2014 Pardi, Elena; Mariotti, Stefano; Pellegata, Natalia S; Benfini, Katiuscia; Borsari, Simona; Saponaro, Federica; Torregrossa, Liborio; Cappai, Antonello; Satta, Chiara; Mastinu, Marco; Marcocci, Claudio; Cetani, Filomena
Functional Characterization of Four Mutations of the Calcium Sensing Receptor Gene Identified in Patients with Familial Hypocalciuric Hypercalcemia Type 1 1-gen-2020 Cetani, Giusy; F, (Cetani; Filomena)(, 1 ); Borsari, Simona; S, (Borsari; Simona)(, 2 ); Pardi, ; E, (Pardi; Elena)(, 2 ); Biagioni, ; T, (Biagioni; Tommaso)(, 2 ); Bagattini, Brunella; B, (Bagattini; Brunella)(, 2 ); Saponaro, Federica; F, (Saponaro; Federica)(, 2 ); Marcocci, Claudio; C, (Marcocci; Claudio)(, 2 )
Gene expression profile in metastatic and non-metastatic parathyroid carcinoma 1-gen-2021 Condello, Vincenzo; Cetani, Filomena; Denaro, Maria; Torregrossa, Liborio; Pardi, Elena; Piaggi, Paolo; Borsari, Simona; Poma, Anello Marcello; Muscarella, Lucia Anna; Graziano, Paolo; Grazia Chiofalo, Maria; Repaci, Andrea; Tallini, Giovanni; Boi, Francesco; Materazzi, Gabriele; Basolo, Fulvio; Marcocci, Claudio