Santostasi T - Search Results

1

Prevalence of atopic symptoms among blood donor carriers of mannose-binding lectin variant alleles.

Cardinale F, Chinellato I, Marseglia GL, Nettis E, Polizzi A, Loffredo MS, Santostasi T, Tesse R, Trerotoli P, Di Monte D, Armenio L. Cardinale F, et al. Among authors: santostasi t. Int J Immunopathol Pharmacol. 2008 Jul-Sep;21(3):735-8. doi: 10.1177/039463200802100329. Int J Immunopathol Pharmacol. 2008. PMID: 18831943 Free article.

2

Association of beta-defensin-1 gene polymorphisms with Pseudomonas aeruginosa airway colonization in cystic fibrosis.

Tesse R, Cardinale F, Santostasi T, Polizzi A, Manca A, Mappa L, Iacoviello G, De Robertis F, Logrillo VP, Armenio L. Tesse R, et al. Among authors: santostasi t. Genes Immun. 2008 Jan;9(1):57-60. doi: 10.1038/sj.gene.6364440. Epub 2007 Oct 25. Genes Immun. 2008. PMID: 17960157

3

Association of interleukin-10 gene haplotypes with Pseudomonas aeruginosa airway colonization in cystic fibrosis.

Tesse R, Cardinale F, Santostasi T, Polizzi A, Mappa L, Manca A, De Robertis F, Silecchia O, Armenio L. Tesse R, et al. Among authors: santostasi t. J Cyst Fibros. 2008 Jul;7(4):329-332. doi: 10.1016/j.jcf.2007.11.004. Epub 2008 Feb 21. J Cyst Fibros. 2008. PMID: 18093884 Free article.

4

Genotype-phenotype correlation in cystic fibrosis patients bearing [H939R;H949L] allele.

Polizzi A, Tesse R, Santostasi T, Diana A, Manca A, Logrillo VP, Cazzato MD, Pantaleo MG, Armenio L. Polizzi A, et al. Among authors: santostasi t. Genet Mol Biol. 2011 Jul;34(3):416-20. doi: 10.1590/S1415-47572011000300008. Epub 2011 Jul 1. Genet Mol Biol. 2011. PMID: 21931512 Free PMC article.

5

A large deletion causes apparent homozygosity for the D1152H mutation in the cystic fibrosis transmembrane regulator (CFTR) gene.

Diana A, Tesse R, Polizzi AM, Santostasi T, Manca A, Leonetti G, Seia M, Porcaro L, Cavallo L. Diana A, et al. Among authors: santostasi t. Gene. 2012 Apr 10;497(1):90-2. doi: 10.1016/j.gene.2012.01.061. Epub 2012 Jan 31. Gene. 2012. PMID: 22310382

6

Comprehensive cystic fibrosis mutation epidemiology and haplotype characterization in a southern Italian population.

Castaldo G, Polizzi A, Tomaiuolo R, Cazeneuve C, Girodon E, Santostasi T, Salvatore D, Raia V, Rigillo N, Goossens M, Salvatore F. Castaldo G, et al. Among authors: santostasi t. Ann Hum Genet. 2005 Jan;69(Pt 1):15-24. doi: 10.1046/j.1529-8817.2004.00130.x. Ann Hum Genet. 2005. PMID: 15638824

7

[The T-lymphocytes in allergic asthmatic children: influence in-vitro of thymostimulin of E rosette forming activity].

Armenio L, Diaferia P, Patano M, Santostasi T, Brunetti L, Spadavecchia F, Mingozzi A, Altavilla P. Armenio L, et al. Among authors: santostasi t. Pediatria (Napoli). 1981 Sep 30;89(3):297-303. Pediatria (Napoli). 1981. PMID: 6981095 Italian. No abstract available.

8

The novel complex allele [A238V;F508del] of the CFTR gene: clinical phenotype and possible implications for cystic fibrosis etiological therapies.

Diana A, Polizzi AM, Santostasi T, Ratclif L, Pantaleo MG, Leonetti G, Iusco DR, Gallo C, Conese M, Manca A. Diana A, et al. Among authors: santostasi t. J Hum Genet. 2016 Jun;61(6):473-81. doi: 10.1038/jhg.2016.15. Epub 2016 Feb 25. J Hum Genet. 2016. PMID: 26911355

9

Retrospective analysis of microorganisms isolated from cystic fibrosis patients in Southern Italy, 2002-2010.

Montagna MT, Barbuti G, Paglionico F, Lovero G, Iatta R, De Giglio O, Cuna T, Coretti C, Santostasi T, Polizzi A, Manca A, Caggiano G, Bouchara JP. Montagna MT, et al. Among authors: santostasi t. J Prev Med Hyg. 2011 Dec;52(4):209-14. J Prev Med Hyg. 2011. PMID: 22442927

10

Phenotypic expression of genotype-phenotype correlation in cystic fibrosis patients carrying the 852del22 mutation.

Polizzi A, Francavilla R, Castaldo G, Santostasi T, Tomaiuolo R, Manca A, De Robertis F, Mappa L, Oliverio FP, Salvatore F, Rigillo N. Polizzi A, et al. Among authors: santostasi t. Am J Med Genet A. 2005 Feb 1;132A(4):434-40. doi: 10.1002/ajmg.a.30493. Am J Med Genet A. 2005. PMID: 15633186

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