PARDI, ELENA Statistiche

PARDI, ELENA  

DIPARTIMENTO DI MEDICINA CLINICA E SPERIMENTALE  

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Risultati 1 - 20 di 34 (tempo di esecuzione: 0.044 secondi).
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A new mutation of the MEN1 gene in an italian kindred with multiple endocrine neoplasia type 1 1-gen-1999 Cetani, F; Pardi, Elena; Cianferotti, Luisella; Vignali, E; Picone, Angelo; Miccoli, Paolo; Pinchera, Aldo; Marcocci, Claudio
Atypical parathyroid adenomas: Challenging lesions in the differential diagnosis of endocrine tumors 1-gen-2019 Cetani, F.; Marcocci, C.; Torregrossa, L.; Pardi, E.
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/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
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 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
First evidence of TRPV5 and TRPV6 channels in human parathyroid glands: possible involvement in neoplastic transformation. 1-gen-2014 Giusti, Laura; Cetani, F; DA VALLE, Ylenia; Pardi, Elena; Ciregia, Federica; Donadio, Elena; Gargini, MARIA CLAUDIA; Piano, Ilaria; Borsari, S; Jaber, Ali; Caputo, Antonella; Basolo, Fulvio; Giannaccini, Gino; Marcocci, Claudio; Lucacchini, Antonio
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
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
Hypercalciuria: its value as a predictive risk factor for nephrolithiasis in asymptomatic primary hyperparathyroidism? 1-gen-2019 Saponaro, F; Cetani, F; Mazoni, L; Apicella, M; Di Giulio, M; Carlucci, F; Scalese, M; Pardi, E; Borsari, S; Bilezikian, J P; Marcocci, C
Incidental occurrence of metastatic medullary thyroid carcinoma in a patient with multiple endocrine neoplasia type 1 carrying germline MEN1 and somatic RET mutations 1-gen-2017 Cetani, Filomena; Pardi, Elena; Berardi, Valentina; Romei, Cristina; Marcocci, Claudio; Elisei, Rossella
Large genomic deletions inactivate the MEN1 gene in Multiple Endocrine Neoplasia (MEN1) families 1-gen-2014 Cetani, F; Pardi, E; Borsari, S; Saponaro, F; Banti, C; Vignali, E; Picone, A; Meola, A; Marcocci, C
Late-onset postsurgical hypoparathyroidism following parathyroidectomy for recurrent primary hyperparathyroidism: a case report and literature review 1-gen-2020 Semeraro, A.; Kemp, E. H.; Pardi, E.; Di Certo, A.; Marcocci, C.; Cetani, F.
Loss of p27 expression is associated with MEN1 gene mutations in sporadic parathyroid adenomas 1-gen-2016 Borsari, Simona; Pardi, Elena; Pellegata, Natalia S.; Lee, Misu; Saponaro, Federica; Torregrossa, Liborio; Basolo, Fulvio; Paltrinieri, Elena; Zatelli, Maria Chiara; Materazzi, Gabriele; Miccoli, Paolo; Marcocci, Claudio; Cetani, Filomena
MEN1 gene alterations do not correlated with the pèhenotype of sporadic primary hyperparathyroidism 1-gen-2002 Cetani, F.; Pardi, Elena; Vignali, E.; Borsari, Simona; Picone, Angelo; Cianferotti, Luisella; Ambrogini, E.; Miccoli, Paolo; Pinchera, Aldo; Marcocci, Claudio
Mutational Analysis of Beta-catenin Exon 3 in Benign and Malignant Parathyroid Tumors. 1-gen-2008 Banti, C; Cetani, F; Pardi, E; Borsari, S; Saponaro, F; Vignali, E; Viccica, G; Cianferotti, L; Ambrogini, E; Pinchera, A; Marcocci, C
Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features 1-gen-2017 Pardi, Elena; Borsari, Simona; Saponaro, Federica; Bogazzi, Fausto; Urbani, Claudio; Mariotti, Stefano; Pigliaru, Francesca; Satta, Chiara; Pani, Fabiana; Materazzi, Gabriele; Miccoli, Paolo; Grantaliano, Lorena; Marcocci, Claudio; Cetani, Filomena