PARDI, ELENA Statistiche
PARDI, ELENA
DIPARTIMENTO DI MEDICINA CLINICA E SPERIMENTALE
A new mutation of the MEN1 gene in an italian kindred with multiple endocrine neoplasia type 1
1999-01-01 Cetani, F; Pardi, Elena; Cianferotti, Luisella; Vignali, E; Picone, Angelo; Miccoli, Paolo; Pinchera, Aldo; Marcocci, Claudio
A Novel Mutation in the Calcium Sensing Receptor Gene in an Italian Family Affected by Autosomal Dominant Hypocalcemia
2018-01-01 Cetani, F; Borsari, S; Saponaro, F; Pardi, E; Banti, C; Mazoni, L; Apicella, M; Marcocci, C
A Prospective Study on Juvenile Primary Hyperparathyroidism Population.
2014-01-01 Saponaro, F; Cacciato, F; Pardi, E; Borsari, S; Marcocci, C; Cetani, F
Atypical parathyroid adenomas: Challenging lesions in the differential diagnosis of endocrine tumors
2019-01-01 Cetani, F.; Marcocci, C.; Torregrossa, L.; Pardi, E.
Beta-catenin activation is not involved in sporadic parathyroid carcinomas and adenomas
2010-01-01 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
2013-01-01 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
2018-01-01 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
2020-01-01 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?
2021-01-01 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.
2017-01-01 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
2014-01-01 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.
2014-01-01 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)
2014-01-01 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
2021-01-01 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?
2019-01-01 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
2017-01-01 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
2014-01-01 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
2020-01-01 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
2016-01-01 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
2002-01-01 Cetani, F.; Pardi, Elena; Vignali, E.; Borsari, Simona; Picone, Angelo; Cianferotti, Luisella; Ambrogini, E.; Miccoli, Paolo; Pinchera, Aldo; Marcocci, Claudio
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
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 | |
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 | |
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 |