Search Results - "Giglio, Luisella"

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  1. 1

    Splicing Factors Induce Cystic Fibrosis Transmembrane Regulator Exon 9 Skipping through a Nonevolutionary Conserved Intronic Element by Pagani, Franco, Buratti, Emanuele, Stuani, Cristiana, Romano, Maurizio, Zuccato, Elisabetta, Niksic, Martina, Giglio, Luisella, Faraguna, Dino, Baralle, Francisco E.

    Published in The Journal of biological chemistry (14-07-2000)
    “…In monosymptomatic forms of cystic fibrosis such as congenital bilateral absence of vas deferens, variations in the TGm and Tn polymorphic repeats at the 3′…”
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    MBL2 polymorphisms screening in a regional Italian CF Center by Trevisiol, Chiara, Boniotto, Michele, Giglio, Luisella, Poli, Furio, Morgutti, Marcello, Crovella, Sergio

    Published in Journal of cystic fibrosis (01-09-2005)
    “…We performed MBL2 genotyping in 47 CF patients—cared of at the regional CF Centre of Trieste—trying to establish a correlation within allelic variants of MBL2…”
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    Early antibiotic treatment of pseudomonas aeruginosa colonisation in cystic fibrosis: a critical review of the literature by MARCHETTI, Federico, GIGLIO, Luisella, CANDUSSO, Manila, FARAGUNA, Dino, ASSAEL, Baroukh M

    Published in European journal of clinical pharmacology (01-04-2004)
    “…To assess the evidence supporting early antibiotic treatment in asymptomatic cystic fibrosis (CF) patients colonised by Pseudomonas aeruginosa (PA). We carried…”
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  6. 6

    Microbiological characterisation of Burkholderia cepacia isolates from cystic fibrosis patients: investigation of the exopolysaccharides produced by Lagatolla, Cristina, Skerlavaj, Silvia, Dolzani, Lucilla, Tonin, Enrico A., Monti Bragadin, Carlo, Bosco, Marco, Rizzo, Roberto, Giglio, Luisella, Cescutti, Paola

    Published in FEMS microbiology letters (19-03-2002)
    “…Abstract Eleven strains of Burkholderia cepacia were isolated directly from clinical specimens: 10 from sputum of cystic fibrosis patients, and one from a…”
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  7. 7

    The Italian registry for cystic fibrosis: what has changed in the last decade by Viviani, Laura, Padoan, Rita, Giglio, Luisella, Bossi, Anna

    Published in Epidemiologia e prevenzione (01-03-2003)
    “…Cystic Fibrosis is the most common life-shortening autosomal recessive disease of Caucasian population. The clinical expression of the disease is heterogeneous…”
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  8. 8

    Microbiological characterisation of Burkholderia cepacia isolates from cystic fibrosis patients: investigation of the exopolysaccharides produced by Lagatolla, Cristina, Skerlavaj, Silvia, Dolzani, Lucilla, Tonin, Enrico A., Monti Bragadin, Carlo, Bosco, Marco, Rizzo, Roberto, Giglio, Luisella, Cescutti, Paola

    Published in FEMS microbiology letters (19-03-2002)
    “…Eleven strains of Burkholderia cepacia were isolated directly from clinical specimens: 10 from sputum of cystic fibrosis patients, and one from a vaginal swab…”
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    Journal Article
  9. 9

    Clinical outcome of fetal uropathy. I. Predictive value of prenatal echography positive for obstructive uropathy by Paduano, L, Giglio, L, Bembi, B, Peratoner, L, D'Ottavio, G, Benussi, G

    Published in The Journal of urology (01-10-1991)
    “…Clinical followup was performed in 73 neonates with a prenatal echographic suspicion of uropathy. Of 42 patients with a prenatal suspicion of unilateral…”
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  10. 10

    Clinical outcome of fetal uropathy. II. Sensitivity of echography for prenatal detection of obstructive pathology by Paduano, L, Giglio, L, Bembi, B, Peratoner, L, Benussi, G

    Published in The Journal of urology (01-10-1991)
    “…Among 8,579 neonates born between February 1, 1981 and March 31, 1987, and cleared by prenatal sonography for significant urinary tract abnormality 158…”
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