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Two diagnostic pitfalls mimicking a prolactin-secreting microadenoma.
D'Ercole M, Della Pepa GM, Carrozza C, Bianchi A, Doglietto F. D'Ercole M, et al. Among authors: carrozza c. J Clin Endocrinol Metab. 2010 Dec;95(12):5171. doi: 10.1210/jc.2010-1913. J Clin Endocrinol Metab. 2010. PMID: 21131538 No abstract available.
CYP21A2 intronic variants causing 21-hydroxylase deficiency.
Concolino P, Rizza R, Costella A, Carrozza C, Zuppi C, Capoluongo E. Concolino P, et al. Among authors: carrozza c. Metabolism. 2017 Jun;71:46-51. doi: 10.1016/j.metabol.2017.03.003. Epub 2017 Mar 9. Metabolism. 2017. PMID: 28521877 Review.
A novel MEN1 frameshift germline mutation in two Italian monozygotic twins.
Concolino P, Rossodivita A, Carrozza C, Raffaelli M, Lombardi CP, Rigante D, Pitocco D, Stabile A, Bellantone R, Zuppi C, Capoluongo E. Concolino P, et al. Among authors: carrozza c. Clin Chem Lab Med. 2008;46(6):824-6. doi: 10.1515/CCLM.2008.165. Clin Chem Lab Med. 2008. PMID: 18601604
72 results