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TOSCO, ANTONELLA

TOSCO, ANTONELLA  

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Intestinal deposits of IgA anti tissue transglutaminase antibodies in celiac children under two years of age. 4.1 Articoli in Atti di convegno 2007 Tosco, Antonella; Maglio, Mariantonia; Paparo, Francesco; Colicchio, B; Sannino, A; Granata, V; Rapacciuolo, L; Troncone, Riccardo
Serum and intestinal IGA anti-tissue transglutaminase antibodies in celiac children under 2 years of age. 4.1 Articoli in Atti di convegno 2007 Tosco, Antonella; Maglio, Mariantonia; Paparo, Francesco; Colicchio, B; Sannino, A; Granata, V; Agnese, Maura; Rapacciuolo, L; Troncone, Riccardo
Potential celiac patients: a model of celiac disease pathogenesis. 1.1 Articolo in rivista 2011 Sperandeo, Mp; Tosco, Antonella; Izzo, Valentina; Tucci, Francesca; Troncone, Riccardo; Auricchio, Renata; Romanos, J; Trynka, G; Auricchio, Salvatore; Jabri, B; Greco, Luigi
Intestinal anti-tissue transglutaminase antibodies in potential coeliac disease. 1.1 Articolo in rivista 2013 Tosco, Antonella; Aitoro, Rosita; Auricchio, Renata; Ponticelli, D; Miele, Erasmo; Paparo, F; Greco, Luigi; Troncone, Riccardo; Maglio, Mariantonia
Clinical, HLA and small bowel immunohistochemical features of children with positive serum antiendomysium antibodies and architecturally normal small intestinal mucosa. 1.1 Articolo in rivista 2005 Paparo, F; Petrone, E; Tosco, Antonella; Maglio, Mariantonia; Borrelli, M; Salvati, Mv; Miele, Erasmo; Greco, Luigi; Auricchio, Salvatore; Troncone, Riccardo
Manipulating proteostasis to repair the F508del-CFTR defect in cystic fibrosis 1.1 Articolo in rivista 2016 Esposito, Speranza; Tosco, Antonella; Villella, Valeria R; Raia, Valeria; Kroemer, Guido; Maiuri, Luigi
Lung structure and function similarities between primary ciliary dyskinesia and mild cystic fibrosis: a pilot study 1.1 Articolo in rivista 2017 Maglione, Marco; Montella, Silvia; Mollica, Carmine; Carnovale, Vincenzo; Iacotucci, Paola; DE GREGORIO, Fabiola; Tosco, Antonella; Cervasio, Mariarosaria; Raia, Valeria; Santamaria, Francesca
Cysteamine re-establishes the clearance of Pseudomonas aeruginosa by macrophages bearing the cystic fibrosis-relevant F508del-CFTR mutation 1.1 Articolo in rivista 2017 Ferrari, Eleonora; Monzani, Romina; Villella, VALERIA RACHELA; Esposito, Speranza; Saluzzo, Francesca; Rossin, Federica; D'Eletto, Manuela; Tosco, Antonella; DE GREGORIO, Fabiola; Izzo, Valentina; Maiuri, MARIA CHIARA; Kroemer, Guido; Raia, Valeria; Maiuri, Luigi
Intra-individual biological variation in sweat chloride concentrations in CF, CFTR dysfunction, and healthy pediatric subjects 1.1 Articolo in rivista 2018 Cirilli, Natalia; Raia, Valeria; Rocco, Ilaria; De Gregorio, Fabiola; Tosco, Antonella; Salvadori, Laura; Sepe, Angela Ornella; Buzzetti, Roberto; Minicuci, Nadia; Castaldo, Giuseppe
Intestinal titres of anti-tissue transglutaminase 2 antibodies correlate positively with mucosal damage degree and inversely with gluten-free diet duration in celiac disease. 1.1 Articolo in rivista 2014 Tosco, A; Auricchio, Renata; Aitoro, R; Ponticelli, D; Primario, M; Miele, Erasmo; Rotondi Aufiero, V; Discepolo, V; Greco, Luigi; Troncone, Riccardo; Maglio, Mariantonia
Methicillin-resistant Staphylococcus aureus eradication in cystic fibrosis patients: A randomized multicenter study 1.1 Articolo in rivista 2019 Dolce, Daniela; Stella, Neri; Grisotto, Laura; Campana, Silvia; Ravenni, Novella; Miselli, Francesca; Camera, Erica; Zavataro, Lucia; Braggion, Cesare; Fiscarelli, Ersilia V.; Lucidi, Vincenzina; Cariani, Lisa; Girelli, Daniela; Faelli, Nadia; Colombo, Carla; Lucanto, Cristina; Lombardo, Mariangela; Magazzù, Giuseppe; Tosco, Antonella; Raia, Valeria; Manara, Serena; Pasolli, Edoardo; Armanini, Federica; Segata, Nicola; Biggeri, Annibale; Taccetti, Giovanni
Immunoglobulin A anti-tissue transglutaminase antibody deposits in the small intestinal mucosa of children with no villous atrophy. 1.1 Articolo in rivista 2008 Tosco, Antonella; Maglio, Mariantonia; Paparo, Francesco; Rapacciuolo, L; Sannino, A; Miele, Erasmo; Barone, MARIA VITTORIA; Auricchio, Renata; Troncone, Riccardo
Discriminant score for celiac disease based on immunohistochemical analysis of duodenal biopsies 1.1 Articolo in rivista 2015 Tosco, Antonella; Maglio, Mariantonia; Paparo, F; Greco, Luigi; Troncone, Riccardo; Auricchio, Renata
NMR for screening and a biochemical assay: Identification of new FPPS inhibitors exerting anticancer activity 1.1 Articolo in rivista 2020 Grimaldi, M.; Randino, R.; Ciaglia, E.; Scrima, M.; Buonocore, M.; Stillitano, I.; Abate, M.; Covelli, V.; Tosco, A.; Gazzerro, P.; Bifulco, M.; Rodriquez, M.; D'Ursi, A. M.
A novel treatment of cystic fibrosis acting on-target: cysteamine plus epigallocatechin gallate for the autophagy-dependent rescue of class II-mutated CFTR 1.1 Articolo in rivista 2016 Tosco, Antonella; de Gregorio, F.; Esposito, S.; de Stefano, D.; Sana, I.; Ferrari, E.; Sepe, A.; Salvadori, L.; Buonpensiero, Paolo; Di Pasqua, A.; Grassia, R.; Leone, C. A.; Guido, Stefano; DE ROSA, Giuseppe; Lusa, Sara; Bona, G.; Stoll, G.; Maiuri, MARIA CHIARA; Mehta, A.; Kroemer, G.; Maiuri, L.; Raia, Valeria
Elevated sweat chloride test: is it always cystic fibrosis 1.1 Articolo in rivista 2021 Cimbalo, C; Tosco, A; Terlizzi, V; Sepe, A; Castaldo, A; Salvadori, L; Raia, V.
Non-invasive tools for detection of liver disease in children and adolescents with cystic fibrosis. 1.1 Articolo in rivista 2021 Tosco, A; Sepe, A; Castaldo, A; Catzola, A; Cimbalo, C; Angelini, V; Vallone, G; Buzzetti, R; Raia, V; Caprio, Mg.
Long-term benefits of nusinersen in a child affected by cystic fibrosis and spinal muscular atrophy type 1. 1.1 Articolo in rivista 2021 Bruno, G; Donnarumma, B; Inverardi, A; Buonpensiero, P; Sepe, A; Tosco, A; Raia, V; Varone, A
A survey of the prevalence, management and outcome of infants with an inconclusive diagnosis following newborn bloodspot screening for cystic fibrosis (CRMS/CFSPID) in six Italian centres. 1.1 Articolo in rivista 2021 Terlizzi, V; Claut, L; Tosco, A; Colombo, C; Raia, V; Fabrizzi, B; Lucarelli, M; Angeloni, A; Cimino, G; Castaldo, A; Marsiglio, L; Timpano, S; Cirilli, N; Moroni, L; Festini, F; Piccinini, P; Zavataro, L; Bonomi, P; Taccetti, G; Southern, Kw; Padoan, R.
Glucose Tolerance Stages in Cystic Fibrosis Are Identified by a Unique Pattern of Defects of Beta-Cell Function. 1.1 Articolo in rivista 2021 Piona, C; Volpi, S; Zusi, C; Mozzillo, E; Tosco, A; Franzese, A; Raia, V; Boselli, Ml; Trombetta, M; Cipolli, M; Bonadonna, Rc; Maffeis, C.