Salvatore D - Search Results

1

An overview of international literature from cystic fibrosis registries: 1. Mortality and survival studies in cystic fibrosis.

Buzzetti R, Salvatore D, Baldo E, Forneris MP, Lucidi V, Manunza D, Marinelli I, Messore B, Neri AS, Raia V, Furnari ML, Mastella G. Buzzetti R, et al. Among authors: salvatore d. J Cyst Fibros. 2009 Jul;8(4):229-37. doi: 10.1016/j.jcf.2009.04.001. Epub 2009 May 6. J Cyst Fibros. 2009. PMID: 19419909 Free article. Review.

2

Lung involvement, the delta F508 mutation and DNA haplotype analysis in cystic fibrosis.

Santamaria F, Salvatore D, Castiglione O, Raia V, de Ritis G, Sebastio G. Santamaria F, et al. Among authors: salvatore d. Hum Genet. 1992 Mar;88(6):639-41. doi: 10.1007/BF02265288. Hum Genet. 1992. PMID: 1348048

3

Cisapride and cystic fibrosis.

Santamaria F, Oggero V, Raia V, Salvatore D, Vittoria L, de Ritis G. Santamaria F, et al. Among authors: salvatore d. J Pediatr Gastroenterol Nutr. 1989 Nov;9(4):539. doi: 10.1097/00005176-198911000-00027. J Pediatr Gastroenterol Nutr. 1989. PMID: 2621534 No abstract available.

4

Molecular epidemiology of cystic fibrosis mutations and haplotypes in southern Italy evaluated with an improved semiautomated robotic procedure.

Castaldo G, Rippa E, Sebastio G, Raia V, Ercolini P, de Ritis G, Salvatore D, Salvatore F. Castaldo G, et al. Among authors: salvatore d, salvatore f. J Med Genet. 1996 Jun;33(6):475-9. doi: 10.1136/jmg.33.6.475. J Med Genet. 1996. PMID: 8782047 Free PMC article.

5

Clinical features of cystic fibrosis patients with rare genotypes.

Castaldo G, Rippa E, Raia V, Salvatore D, Massa C, de Ritis G, Salvatore F. Castaldo G, et al. Among authors: salvatore d, salvatore f. J Med Genet. 1996 Jan;33(1):73-6. doi: 10.1136/jmg.33.1.73. J Med Genet. 1996. PMID: 8825054 Free PMC article.

6

Severe liver impairment in a cystic fibrosis-affected child homozygous for the G542X mutation.

Castaldo G, Rippa E, Salvatore D, Sibillo R, Raia V, de Ritis G, Salvatore F. Castaldo G, et al. Among authors: salvatore d, salvatore f. Am J Med Genet. 1997 Mar 17;69(2):155-8. doi: 10.1002/(sici)1096-8628(19970317)69:2<155::aid-ajmg7>3.0.co;2-o. Am J Med Genet. 1997. PMID: 9056552 Review.

7

[Italian Cystic Fibrosis Registry: 10 years of activity].

Bossi A, Battistini F, Braggion C, Magno EC, Cosimi A, de Candussio G, Gagliardini R, Giglio L, Giunta A, Grzincich GL, La Rosa M, Lombardo M, Lucidi V, Manca A, Mastella G, Moretti P, Padoan R, Pardo F, Quattrucci S, Raia V, Romano L, Salvatore D, Taccetti G, Zanda M. Bossi A, et al. Among authors: salvatore d. Epidemiol Prev. 1999 Jan-Mar;23(1):5-16. Epidemiol Prev. 1999. PMID: 10356860 Italian.

8

Detection of five rare cystic fibrosis mutations peculiar to Southern Italy: implications in screening for the disease and phenotype characterization for patients with homozygote mutations.

Castaldo G, Fuccio A, Cazeneuve C, Picci L, Salvatore D, Raia V, Scarpa M, Goossens M, Salvatore F. Castaldo G, et al. Among authors: salvatore d, salvatore f. Clin Chem. 1999 Jul;45(7):957-62. Clin Chem. 1999. PMID: 10388469

9

Phenotype/genotype correlation and cystic fibrosis related diabetes mellitus (Italian Multicenter Study).

Cotellessa M, Minicucci L, Diana MC, Prigione F, Di Febbraro L, Gagliardini R, Manca A, Battistini F, Taccetti G, Magazzù G, Padoan R, Pizzamiglio G, Raia V, Iapichino L, Cardella F, Grinzich G, Lucidi V, Tuccio G, Bignamini E, Salvatore D, Lorini R. Cotellessa M, et al. Among authors: salvatore d. J Pediatr Endocrinol Metab. 2000 Sep-Oct;13(8):1087-93. doi: 10.1515/jpem.2000.13.8.1087. J Pediatr Endocrinol Metab. 2000. PMID: 11085186

10

Liver expression in cystic fibrosis could be modulated by genetic factors different from the cystic fibrosis transmembrane regulator genotype.

Castaldo G, Fuccio A, Salvatore D, Raia V, Santostasi T, Leonardi S, Lizzi N, La Rosa M, Rigillo N, Salvatore F. Castaldo G, et al. Among authors: salvatore d, salvatore f. Am J Med Genet. 2001 Feb 1;98(4):294-7. doi: 10.1002/1096-8628(20010201)98:4<294::aid-ajmg1097>3.0.co;2-k. Am J Med Genet. 2001. PMID: 11170070

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