Mantero F - Search Results

1

Deletion within the CYP17 gene together with insertion of foreign DNA is the cause of combined complete 17 alpha-hydroxylase/17,20-lyase deficiency in an Italian patient.

Biason A, Mantero F, Scaroni C, Simpson ER, Waterman MR. Biason A, et al. Among authors: mantero f. Mol Endocrinol. 1991 Dec;5(12):2037-45. doi: 10.1210/mend-5-12-2037. Mol Endocrinol. 1991. PMID: 1665206

2

17-alpha-hydroxylase deficiency in three siblings: short- and long-term studies.

Scaroni C, Biason A, Carpenè G, Opocher G, Mantero F. Scaroni C, et al. Among authors: mantero f. J Endocrinol Invest. 1991 Feb;14(2):99-108. doi: 10.1007/BF03350278. J Endocrinol Invest. 1991. PMID: 1648117

3

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

4

No linkage between HLA and congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency.

Mantero F, Scaroni C, Pasini CV, Fagiolo U. Mantero F, et al. N Engl J Med. 1980 Aug 28;303(9):530. doi: 10.1056/nejm198008283030923. N Engl J Med. 1980. PMID: 6967187 No abstract available.

5

HLA and hormonal data for identification of heterozygotes in 11 beta- and 17 alpha-hydroxylase deficiency syndromes.

Mantero F, Scaroni C, Masarotto P, Pasini CV. Mantero F, et al. Clin Exp Pharmacol Physiol. 1982 May-Jun;9(3):265-9. doi: 10.1111/j.1440-1681.1982.tb00805.x. Clin Exp Pharmacol Physiol. 1982. PMID: 6291824

6

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

7

Renin-angiotensin-aldosterone system: a long-term follow-up study in 17 alpha-hydroxylase deficiency syndrome (17OHDS).

Scaroni C, Opocher G, Mantero F. Scaroni C, et al. Among authors: mantero f. Clin Exp Hypertens A. 1986;8(4-5):773-80. doi: 10.3109/10641968609046593. Clin Exp Hypertens A. 1986. PMID: 3530552

8

HLA and hormonal studies in 5 patients with late-onset 21-hydroxylase deficiency syndrome (21OHDS).

Scaroni C, Orlandini E, Venturi Pasini C, Gangemi M, Mantero F. Scaroni C, et al. Among authors: mantero f. J Endocrinol Invest. 1986 Feb;9(1):65-70. doi: 10.1007/BF03348067. J Endocrinol Invest. 1986. PMID: 3009598

9

HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiency.

Pollack MS, New MI, O'Neill GJ, Levine LS, Callaway C, Pang S, 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, Dupont B. Pollack MS, et al. Among authors: mantero f. Hum Genet. 1981;58(3):331-7. doi: 10.1007/BF00294933. Hum Genet. 1981. PMID: 6948766

10

Low-dose ketoconazole treatment in hirsute women.

Sonino N, Scaroni C, Biason A, Boscaro M, Mantero F. Sonino N, et al. Among authors: mantero f. J Endocrinol Invest. 1990 Jan;13(1):35-40. doi: 10.1007/BF03348578. J Endocrinol Invest. 1990. PMID: 2138647

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