Pirazzoli P - Search Results

1

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: pirazzoli p. Clin Endocrinol (Oxf). 2000 Jul;53(1):117-25. doi: 10.1046/j.1365-2265.2000.01048.x. Clin Endocrinol (Oxf). 2000. PMID: 10931088

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: pirazzoli p. 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

Congenital adrenal hyperplasia: neonatal mass screening compared with clinical diagnosis only in the Emilia-Romagna region of Italy, 1980-1995.

Balsamo A, Cacciari E, Piazzi S, Cassio A, Bozza D, Pirazzoli P, Zappulla F. Balsamo A, et al. Among authors: pirazzoli p. Pediatrics. 1996 Sep;98(3 Pt 1):362-7. Pediatrics. 1996. PMID: 8784357

4

Birth weight affects final height in patients treated for growth hormone deficiency.

Cacciari E, Zucchini S, Cicognani A, Pirazzoli P, Balsamo A, Salardi S, Cassio A, Pasini A, Gualandi S. Cacciari E, et al. Among authors: pirazzoli p. Clin Endocrinol (Oxf). 1999 Dec;51(6):733-9. doi: 10.1046/j.1365-2265.1999.00875.x. Clin Endocrinol (Oxf). 1999. PMID: 10619978

5

Functional analysis of two recurrent amino acid substitutions in the CYP21 gene from Italian patients with congenital adrenal hyperplasia.

Barbaro M, Lajic S, Baldazzi L, Balsamo A, Pirazzoli P, Cicognani A, Wedell A, Cacciari E. Barbaro M, et al. Among authors: pirazzoli p. J Clin Endocrinol Metab. 2004 May;89(5):2402-7. doi: 10.1210/jc.2003-031630. J Clin Endocrinol Metab. 2004. PMID: 15126570

6

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

7

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: pirazzoli p. 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.

8

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: pirazzoli p. 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.

9

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: pirazzoli p. J Clin Endocrinol Metab. 1992 Jun;74(6):1284-9. doi: 10.1210/jcem.74.6.1592872. J Clin Endocrinol Metab. 1992. PMID: 1592872

10

Variability of growth hormone response to pharmacological and sleep tests performed twice in short children.

Tassoni P, Cacciari E, Cau M, Colli C, Tosi M, Zucchini S, Cicognani A, Pirazzoli P, Salardi S, Balsamo A, et al. Tassoni P, et al. Among authors: pirazzoli p. J Clin Endocrinol Metab. 1990 Jul;71(1):230-4. doi: 10.1210/jcem-71-1-230. J Clin Endocrinol Metab. 1990. PMID: 2370294

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