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Page 1
Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency.
Levine LS, Dupont B, Lorenzen F, Pang S, Pollack M, Oberfield SE, Kohn B, Lerner A, Cacciari E, Mantero F, Cassio A, Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R, Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, New MI. Levine LS, et al. Among authors: mantero f. J Clin Endocrinol Metab. 1981 Dec;53(6):1193-8. doi: 10.1210/jcem-53-6-1193. J Clin Endocrinol Metab. 1981. PMID: 6271801
Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasia.
Levine LS, Dupont B, Lorenzen F, Pang S, Pollack M, Oberfield S, Kohn B, Lerner A, Cacciari E, Mantero F, Cassio A, Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R, Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, New MI. Levine LS, et al. Among authors: mantero f. J Clin Endocrinol Metab. 1980 Dec;51(6):1316-24. doi: 10.1210/jcem-51-6-1316. J Clin Endocrinol Metab. 1980. PMID: 6449518
Apparent mineralocorticoid excess type II.
Mantero F, Tedde R, Opocher G, Dessi Fulgheri P, Arnaldi G, Ulick S. Mantero F, et al. Steroids. 1994 Feb;59(2):80-3. doi: 10.1016/0039-128x(94)90080-9. Steroids. 1994. PMID: 8191552
Primary aldosteronism due to a malignant ovarian tumor.
Todesco S, Terribile V, Borsatti A, Mantero F. Todesco S, et al. Among authors: mantero f. J Clin Endocrinol Metab. 1975 Nov;41(5):809-19. doi: 10.1210/jcem-41-5-809. J Clin Endocrinol Metab. 1975. PMID: 171276
439 results