Sfoglia per Autore
Six novel MEN1 gene mutations in sporadic parathyroid tumors
2000-01-01 Cetani, F; Pardi, E; Giovannetti, A; Cerrai, P; Borsari, Simona; Vignali, E; Picone, Angelo; Cianferotti, Luisella; Miccoli, Paolo; Pinchera, Aldo; Marcocci, Claudio
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
A reappraisal of the Rb1 gene abnormalities in the diagnosis of parathyroid cancer
2004-01-01 Cetani, F; Pardi, E; Viacava, P; Pollina, Gd; Fanelli, G; Picone, Angelo; Borsari, Simona; Gazzerro, E; Miccoli, Paolo; Berti, Piero; Pinchera, A; Marcocci, Claudio
Different somatic alterations of the HRPT2 gene in a patient with recurrent sporadic primary hyperparathyroidism carrying an HRPT2 germline mutation
2007-01-01 Cetani, F; Pardi, E; Ambrogini, E; Viacava, P; Borsari, Simona; LEMMI GIGLI, Mauro; Cianferotti, Luisella; Miccoli, Paolo; Pinchera, Aldo; Arnold, A; Marcocci, Claudio
Mutational Analysis of Beta-catenin Exon 3 in Benign and Malignant Parathyroid Tumors.
2008-01-01 Banti, C; Cetani, F; Pardi, E; Borsari, S; Saponaro, F; Vignali, E; Viccica, G; Cianferotti, L; Ambrogini, E; Pinchera, A; Marcocci, C
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
CDC73 mutational status and loss of parafibromin in the outcome of parathyroid cancer.
2013-01-01 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
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
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
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
A Prospective Study on Juvenile Primary Hyperparathyroidism Population.
2014-01-01 Saponaro, F; Cacciato, F; Pardi, E; Borsari, S; 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
Primary hyperparathyroidism due to atypical adenoma: clinical, biochemical and histological features of an Italian cohort
2017-01-01 Cetani, F; Saponaro, F; Di Giulio, M; Pardi, E; Borsari, S; Marcocci, C
Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features
2017-01-01 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
Familial hypocalciuric hypercalcemia type 1 due to a novel homozygous mutation of the calcium-sensing receptor gene
2017-01-01 Borsari, Simona; Marcocci, Claudio; Cetani, F.
Loss of p27 expression is associated with MEN1 gene mutations in sporadic parathyroid adenomas
2017-01-01 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
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
Vitamin D measurement and effect on outcome in a cohort of patients with heart failure
2018-01-01 Saponaro, Federica; Saba, Alessandro; Frascarelli, Sabina; Prontera, Concetta; Clerico, Aldo; SCALESE URCIUOLI, Marco; Sessa, Maria Rita; Cetani, Filomena; Borsari, Simona; Pardi, Elena; Marvelli, Antonella; Marcocci, Claudio; Passino, Claudio; Zucchi, Riccardo
Familial and Hereditary Forms of Primary Hyperparathyroidism
2018-01-01 Cetani, F.; Saponaro, F.; Borsari, S.; Marcocci, C.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Six novel MEN1 gene mutations in sporadic parathyroid tumors | 1-gen-2000 | Cetani, F; Pardi, E; Giovannetti, A; Cerrai, P; Borsari, Simona; Vignali, E; Picone, Angelo; Cianferotti, Luisella; Miccoli, Paolo; Pinchera, Aldo; Marcocci, Claudio | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| A Prospective Study on Juvenile Primary Hyperparathyroidism Population. | 1-gen-2014 | Saponaro, F; Cacciato, F; Pardi, E; Borsari, S; 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 | |
| Primary hyperparathyroidism due to atypical adenoma: clinical, biochemical and histological features of an Italian cohort | 1-gen-2017 | Cetani, F; Saponaro, F; Di Giulio, M; Pardi, E; Borsari, S; 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 | |
| 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. | |
| Loss of p27 expression is associated with MEN1 gene mutations in sporadic parathyroid adenomas | 1-gen-2017 | 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 | |
| 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 | |
| Vitamin D measurement and effect on outcome in a cohort of patients with heart failure | 1-gen-2018 | Saponaro, Federica; Saba, Alessandro; Frascarelli, Sabina; Prontera, Concetta; Clerico, Aldo; SCALESE URCIUOLI, Marco; Sessa, Maria Rita; Cetani, Filomena; Borsari, Simona; Pardi, Elena; Marvelli, Antonella; Marcocci, Claudio; Passino, Claudio; Zucchi, Riccardo | |
| Familial and Hereditary Forms of Primary Hyperparathyroidism | 1-gen-2018 | Cetani, F.; Saponaro, F.; Borsari, S.; Marcocci, C. |
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