Sfoglia per Autore
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
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
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
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
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
A Prospective Study on Juvenile Primary Hyperparathyroidism Population.
2014-01-01 Saponaro, F; Cacciato, F; Pardi, E; Borsari, S; Marcocci, C; Cetani, F
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
Update on parathyroid carcinoma
2016-01-01 Cetani, F; Pardi, Elena; Marcocci, Claudio
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
Parathyroid carcinoma: a clinical and genetic perspective
2017-01-01 Cetani, Filomena; Pardi, Elena; Marcocci, Claudio
Novel association of MEN1 gene mutations with parathyroid carcinoma
2017-01-01 Cinque, Luigia; Sparaneo, Angelo; Cetani, Filomena; Coco, Michelina; Clemente, Celeste; Chetta, Massimiliano; Balsamo, Teresa; Battista, Claudia; Sanpaolo, Eliana; Pardi, Elena; D'Agruma, Leonardo; Marcocci, Claudio; Maiello, Evaristo; Hendy, Geoffrey N.; Cole, David E. C.; Scillitani, Alfredo; Guarnieri, Vito
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
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
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
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
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 | |
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 | |
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 | |
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 | |
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 | |
A Prospective Study on Juvenile Primary Hyperparathyroidism Population. | 1-gen-2014 | Saponaro, F; Cacciato, F; Pardi, E; Borsari, S; Marcocci, C; Cetani, F | |
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 | |
Update on parathyroid carcinoma | 1-gen-2016 | Cetani, F; Pardi, Elena; Marcocci, Claudio | |
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 | |
Parathyroid carcinoma: a clinical and genetic perspective | 1-gen-2017 | Cetani, Filomena; Pardi, Elena; Marcocci, Claudio | |
Novel association of MEN1 gene mutations with parathyroid carcinoma | 1-gen-2017 | Cinque, Luigia; Sparaneo, Angelo; Cetani, Filomena; Coco, Michelina; Clemente, Celeste; Chetta, Massimiliano; Balsamo, Teresa; Battista, Claudia; Sanpaolo, Eliana; Pardi, Elena; D'Agruma, Leonardo; Marcocci, Claudio; Maiello, Evaristo; Hendy, Geoffrey N.; Cole, David E. C.; Scillitani, Alfredo; Guarnieri, Vito | |
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 | |
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 | |
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 | |
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 |
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