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Page 1
Increased prevalence of the GCM2 polymorphism, Y282D, in primary hyperparathyroidism: analysis of three Italian cohorts.
D'Agruma L, Coco M, Guarnieri V, Battista C, Canaff L, Salcuni AS, Corbetta S, Cetani F, Minisola S, Chiodini I, Eller-Vainicher C, Spada A, Marcocci C, Guglielmi G, Zini M, Clemente R, Wong BY, de Martino D, Scillitani A, Hendy GN, Cole DE. D'Agruma L, et al. Among authors: marcocci c. J Clin Endocrinol Metab. 2014 Dec;99(12):E2794-8. doi: 10.1210/jc.2014-2857. J Clin Endocrinol Metab. 2014. PMID: 25279501
Two Italian kindreds with familial hypocalciuric hypercalcaemia caused by loss-of-function mutations in the calcium-sensing receptor (CaR) gene: functional characterization of a novel CaR missense mutation.
Cetani F, Pardi E, Borsari S, Tonacchera M, Morabito E, Pinchera A, Marcocci C, Dipollina G. Cetani F, et al. Among authors: marcocci c. Clin Endocrinol (Oxf). 2003 Feb;58(2):199-206. doi: 10.1046/j.1365-2265.2003.01696.x. Clin Endocrinol (Oxf). 2003. PMID: 12580936
A reappraisal of the Rb1 gene abnormalities in the diagnosis of parathyroid cancer.
Cetani F, Pardi E, Viacava P, Pollina GD, Fanelli G, Picone A, Borsari S, Gazzerro E, Miccoli P, Berti P, Pinchera A, Marcocci C. Cetani F, et al. Among authors: marcocci c. Clin Endocrinol (Oxf). 2004 Jan;60(1):99-106. doi: 10.1111/j.1365-2265.2004.01954.x. Clin Endocrinol (Oxf). 2004. PMID: 14678295
Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumors.
Cetani F, Pardi E, Borsari S, Viacava P, Dipollina G, Cianferotti L, Ambrogini E, Gazzerro E, Colussi G, Berti P, Miccoli P, Pinchera A, Marcocci C. Cetani F, et al. Among authors: marcocci c. J Clin Endocrinol Metab. 2004 Nov;89(11):5583-91. doi: 10.1210/jc.2004-0294. J Clin Endocrinol Metab. 2004. PMID: 15531515
406 results