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Clinical presentation and management of patients with primary hyperparathyroidism in Italy.
Saponaro F, Cetani F, Repaci A, Pagotto U, Cipriani C, Pepe J, Minisola S, Cipri C, Vescini F, Scillitani A, Salcuni A, Palmieri S, Eller-Vainicher C, Chiodini I, Madeo B, Kara E, Castellano E, Borretta G, Gianotti L, Romanelli F, Camozzi V, Faggiano A, Corbetta S, Cianferotti L, Brandi ML, De Feo ML, Palermo A, Vezzoli G, Maino F, Scalese M, Marcocci C. Saponaro F, et al. Among authors: cianferotti l. J Endocrinol Invest. 2018 Nov;41(11):1339-1348. doi: 10.1007/s40618-018-0879-z. Epub 2018 Apr 3. J Endocrinol Invest. 2018. PMID: 29616419
Six novel MEN1 gene mutations in sporadic parathyroid tumors.
Cetani F, Pardi E, Giovannetti A, Cerrai P, Borsari S, Vignali E, Picone A, Cianferotti L, Miccoli P, Pinchera A, Marcocci C. Cetani F, et al. Among authors: cianferotti l. Hum Mutat. 2000 Nov;16(5):445. doi: 10.1002/1098-1004(200011)16:5<445::AID-HUMU12>3.0.CO;2-6. Hum Mutat. 2000. PMID: 11058905
A novel mutation of the autoimmune regulator gene in an Italian kindred with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy, acting in a dominant fashion and strongly cosegregating with hypothyroid autoimmune thyroiditis.
Cetani F, Barbesino G, Borsari S, Pardi E, Cianferotti L, Pinchera A, Marcocci C. Cetani F, et al. Among authors: cianferotti l. J Clin Endocrinol Metab. 2001 Oct;86(10):4747-52. doi: 10.1210/jcem.86.10.7884. J Clin Endocrinol Metab. 2001. PMID: 11600535
Calcium-sensing receptor gene polymorphisms in primary hyperparathyroidism.
Cetani F, Borsari S, Vignali E, Pardi E, Picone A, Cianferotti L, Rossi G, Miccoli P, Pinchera A, Marcocci C. Cetani F, et al. Among authors: cianferotti l. J Endocrinol Invest. 2002 Jul-Aug;25(7):614-9. doi: 10.1007/BF03345085. J Endocrinol Invest. 2002. PMID: 12150336
108 results