Cicognani A - Search Results

1

A novel PRKAR1A mutation associated with hepatocellular carcinoma in a young patient and a variable Carney complex phenotype in affected subjects in older generations.

Gennari M, Stratakis CA, Hovarth A, Pirazzoli P, Cicognani A. Gennari M, et al. Among authors: cicognani a. Clin Endocrinol (Oxf). 2008 Nov;69(5):751-5. doi: 10.1111/j.1365-2265.2008.03286.x. Epub 2008 Apr 28. Clin Endocrinol (Oxf). 2008. PMID: 18445140 Free PMC article.

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. Among authors: cicognani a. 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

CYP21 genotype, adult height, and pubertal development in 55 patients treated for 21-hydroxylase deficiency.

Balsamo A, Cicognani A, Baldazzi L, Barbaro M, Baronio F, Gennari M, Bal M, Cassio A, Kontaxaki K, Cacciari E. Balsamo A, et al. Among authors: cicognani a. J Clin Endocrinol Metab. 2003 Dec;88(12):5680-8. doi: 10.1210/jc.2003-030123. J Clin Endocrinol Metab. 2003. PMID: 14671153

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: cicognani a. Eur J Endocrinol. 2006 Aug;155(2):201-5. doi: 10.1530/eje.1.02198. Eur J Endocrinol. 2006. PMID: 16868131

5

Effect on adult height of pubertal growth hormone retesting and withdrawal of therapy in patients with previously diagnosed growth hormone deficiency.

Zucchini S, Pirazzoli P, Baronio F, Gennari M, Bal MO, Balsamo A, Gualandi S, Cicognani A. Zucchini S, et al. Among authors: cicognani a. J Clin Endocrinol Metab. 2006 Nov;91(11):4271-6. doi: 10.1210/jc.2006-0383. Epub 2006 Aug 15. J Clin Endocrinol Metab. 2006. PMID: 16912138 Clinical Trial.

6

Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1.

Balsamo A, Cicognani A, Gennari M, Sippell WG, Menabò S, Baronio F, Riepe FG. Balsamo A, et al. Among authors: cicognani a. Eur J Endocrinol. 2007 Feb;156(2):249-56. doi: 10.1530/eje.1.02330. Eur J Endocrinol. 2007. PMID: 17287415

7

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: cicognani a. Horm Res. 2008;70(2):124-8. doi: 10.1159/000137664. Epub 2008 Jun 12. Horm Res. 2008. PMID: 18547961

8

CYP21 analysis and phenotype/genotype relationship in the screened population of the Italian Emilia-Romagna region.

Balsamo A, Cacciari E, Baldazzi L, Tartaglia L, Cassio A, Mantovani V, Piazzi S, Cicognani A, Pirazzoli P, Mainetti B, Zappulla F. Balsamo A, et al. Among authors: cicognani a. Clin Endocrinol (Oxf). 2000 Jul;53(1):117-25. doi: 10.1046/j.1365-2265.2000.01048.x. Clin Endocrinol (Oxf). 2000. PMID: 10931088

9

Active and total ghrelin concentrations in the newborn.

Pirazzoli P, Lanari M, Zucchini S, Gennari M, Pagotto U, De Iasio R, Pasquali R, Cassio A, Cicognani A, Cacciari E. Pirazzoli P, et al. Among authors: cicognani a. J Pediatr Endocrinol Metab. 2005 Apr;18(4):379-84. doi: 10.1515/jpem.2005.18.4.379. J Pediatr Endocrinol Metab. 2005. PMID: 15844472

10

Pitfalls in diagnosing impaired growth hormone (GH) secretion: retesting after replacement therapy of 63 patients defined as GH deficient.

Cacciari E, Tassoni P, Parisi G, Pirazzoli P, Zucchini S, Mandini M, Cicognani A, Balsamo A. Cacciari E, et al. Among authors: cicognani a. J Clin Endocrinol Metab. 1992 Jun;74(6):1284-9. doi: 10.1210/jcem.74.6.1592872. J Clin Endocrinol Metab. 1992. PMID: 1592872

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