Nicoletti A - Search Results

1

Gonadoblastoma in Turner syndrome and Y-chromosome-derived material.

Mazzanti L, Cicognani A, Baldazzi L, Bergamaschi R, Scarano E, Strocchi S, Nicoletti A, Mencarelli F, Pittalis M, Forabosco A, Cacciari E. Mazzanti L, et al. Among authors: nicoletti a. Am J Med Genet A. 2005 Jun 1;135(2):150-4. doi: 10.1002/ajmg.a.30569. Am J Med Genet A. 2005. PMID: 15880570

2

SRD5A2 gene analysis in an Italian population of under-masculinized 46,XY subjects.

Nicoletti A, Baldazzi L, Balsamo A, Barp L, Pirazzoli P, Gennari M, Radetti G, Cacciari E, Cicognani A. Nicoletti A, et al. Clin Endocrinol (Oxf). 2005 Oct;63(4):375-80. doi: 10.1111/j.1365-2265.2005.02348.x. Clin Endocrinol (Oxf). 2005. PMID: 16181229

3

Three novel AMH gene mutations in a patient with persistent mullerian duct syndrome and normal AMH serum dosage.

Menabò S, Balsamo A, Nicoletti A, Gennari M, Pirazzoli P, Cicognani A, Baldazzi L. Menabò S, et al. Among authors: nicoletti a. Horm Res. 2008;70(2):124-8. doi: 10.1159/000137664. Epub 2008 Jun 12. Horm Res. 2008. PMID: 18547961

4

Two novel GnRHR gene mutations in two siblings with hypogonadotropic hypogonadism.

Antelli A, Baldazzi L, Balsamo A, Pirazzoli P, Nicoletti A, Gennari M, Cicognani A. Antelli A, et al. Among authors: nicoletti a. Eur J Endocrinol. 2006 Aug;155(2):201-5. doi: 10.1530/eje.1.02198. Eur J Endocrinol. 2006. PMID: 16868131

5

Thyrotropin-stimulating hormone receptor gene analysis in pediatric patients with non-autoimmune subclinical hypothyroidism.

Nicoletti A, Bal M, De Marco G, Baldazzi L, Agretti P, Menabò S, Ballarini E, Cicognani A, Tonacchera M, Cassio A. Nicoletti A, et al. J Clin Endocrinol Metab. 2009 Nov;94(11):4187-94. doi: 10.1210/jc.2009-0618. Epub 2009 Oct 9. J Clin Endocrinol Metab. 2009. PMID: 19820021

6

Two new point mutations of the SRY gene identified in two Italian 46,XY females with gonadal dysgenesis.

Baldazzi L, Nicoletti A, Gennari M, Barbaro M, Pirazzoli P, Cicognani A, Cacciari E. Baldazzi L, et al. Among authors: nicoletti a. Clin Genet. 2003 Sep;64(3):258-60. doi: 10.1034/j.1399-0004.2003.00125.x. Clin Genet. 2003. PMID: 12919143 No abstract available.

7

A sequence variation in 3'UTR of CYP21A2 gene correlates with a mild form of congenital adrenal hyperplasia.

Menabò S, Balsamo A, Baldazzi L, Barbaro M, Nicoletti A, Conti V, Pirazzoli P, Wedell A, Cicognani A. Menabò S, et al. Among authors: nicoletti a. J Endocrinol Invest. 2012 Mar;35(3):298-305. doi: 10.3275/7680. Epub 2011 Apr 26. J Endocrinol Invest. 2012. PMID: 21521936

8

Current loss-of-function mutations in the thyrotropin receptor gene: when to investigate, clinical effects, and treatment.

Cassio A, Nicoletti A, Rizzello A, Zazzetta E, Bal M, Baldazzi L. Cassio A, et al. Among authors: nicoletti a. J Clin Res Pediatr Endocrinol. 2013;5 Suppl 1(Suppl 1):29-39. doi: 10.4274/jcrpe.864. Epub 2012 Nov 15. J Clin Res Pediatr Endocrinol. 2013. PMID: 23154162 Free PMC article. Review.

9

The SHOX gene: a new indication for GH treatment.

Cicognani A, Pirazzoli P, Nicoletti A, Baronio F, Conti V, Bonetti S. Cicognani A, et al. Among authors: nicoletti a. J Endocrinol Invest. 2010 Jun;33(6 Suppl):15-8. J Endocrinol Invest. 2010. PMID: 21057180

10

17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence.

Bertelloni S, Balsamo A, Giordani L, Fischetto R, Russo G, Delvecchio M, Gennari M, Nicoletti A, Maggio MC, Concolino D, Cavallo L, Cicognani A, Chiumello G, Hiort O, Baroncelli GI, Faienza MF. Bertelloni S, et al. Among authors: nicoletti a. J Endocrinol Invest. 2009 Sep;32(8):666-70. doi: 10.1007/BF03345738. Epub 2009 May 12. J Endocrinol Invest. 2009. PMID: 19498320

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