Piazzi S - 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: piazzi s. 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

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: piazzi s. Pediatrics. 1996 Sep;98(3 Pt 1):362-7. Pediatrics. 1996. PMID: 8784357

3

[Models of the organization of neonatal screening].

Cassio A, Piazzi S, Colli C, Balsamo A, Bozza D, Salardi S, Sprovieri G, Cacciari E. Cassio A, et al. Among authors: piazzi s. Ann Ist Super Sanita. 1994;30(3):269-73. Ann Ist Super Sanita. 1994. PMID: 7879992 Italian.

4

[Results of screening of congenital hypothyroidism and iodine excess in neonatal age].

Cassio A, Colli C, Piazzi S, Bozza D, Zappulla F, Balsamo A, Salardi S, Cacciari E. Cassio A, et al. Among authors: piazzi s. Ann Ist Super Sanita. 1998;34(3):337-41. Ann Ist Super Sanita. 1998. PMID: 10052171 Italian.

5

Neonatal screening for congenital adrenal hyperplasia.

Cacciari E, Balsamo A, Cassio A, Piazzi S, Bernardi F, Salardi S, Cicognani A, Pirazzoli P, Zappulla F, Capelli M, et al. Cacciari E, et al. Among authors: piazzi s. Arch Dis Child. 1983 Oct;58(10):803-6. doi: 10.1136/adc.58.10.803. Arch Dis Child. 1983. PMID: 6639129 Free PMC article.

6

Neonatal screening for congenital adrenal hyperplasia using a microfilter paper method for 17-alpha-hydroxyprogesterone radioimmunoassay. Experience gained from the study of 22,233 cases.

Cacciari E, Balsamo A, Cassio A, Piazzi S, Bernardi F, Salardi S, Cicognani A, Pirazzoli P, Zappulla F, Capelli M, Paolini M. Cacciari E, et al. Among authors: piazzi s. Horm Res. 1982;16(1):4-9. doi: 10.1159/000179479. Horm Res. 1982. PMID: 7068111

7

[Neuropsychological follow-up of children with phenylketonuria treated early].

Salardi S, Missiroli G, Piazzi S, Mandini M, Cassio A, Colli C, Tacconi M, Tolomelli M, Cacciari E. Salardi S, et al. Among authors: piazzi s. Pediatr Med Chir. 1992 Jul-Aug;14(4):409-13. Pediatr Med Chir. 1992. PMID: 1461780 Italian.

8

Neonatal screening for 21-hydroxylase deficiency: a microfilter paper method for 17-alpha-hydroxyprogesterone assay.

Piazzi S, Capelli M, Paolini M, Perugini D, Grossi G, Balsamo A, Salomoni P, Cassio A, Bugiardini G, Cacciari E. Piazzi S, et al. J Endocrinol Invest. 1982 Mar-Apr;5(2):87-90. doi: 10.1007/BF03350496. J Endocrinol Invest. 1982. PMID: 6980238

9

Neonatal screening programme for congenital adrenal hyperplasia in a homogeneous Caucasian population.

Cacciari E, Balsamo A, Cassio A, Piazzi S, Bernardi F, Salardi S, Cicognani A, Pirazzoli P, Zappulla F, Capelli M, et al. Cacciari E, et al. Among authors: piazzi s. J Inherit Metab Dis. 1986;9 Suppl 1:142-6. doi: 10.1007/BF01800868. J Inherit Metab Dis. 1986. PMID: 3097413 No abstract available.

10

Neonatal screening program for congenital adrenal hyperplasia in a homogeneous Caucasian population.

Cacciari E, Balsamo A, Cassio A, Piazzi S, Bernardi F, Salardi S, Cicognani A, Pirazzoli P, Zappulla F, Capelli M, et al. Cacciari E, et al. Among authors: piazzi s. Ann N Y Acad Sci. 1985;458:85-9. doi: 10.1111/j.1749-6632.1985.tb14594.x. Ann N Y Acad Sci. 1985. PMID: 3879135 No abstract available.

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