Search Results - "Sonia Volpi"

Does cystic fibrosis constitute an advantage in COVID-19 infection? by Bezzerri, Valentino, Lucca, Francesca, Volpi, Sonia, Cipolli, Marco

“…The Veneto region is one of the most affected Italian regions by COVID-19. Chronic lung diseases, such as chronic obstructive pulmonary disease (COPD), may…”
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SARS-CoV-2 viral entry and replication is impaired in Cystic Fibrosis airways due to ACE2 downregulation by Bezzerri, Valentino, Gentili, Valentina, Api, Martina, Finotti, Alessia, Papi, Chiara, Tamanini, Anna, Boni, Christian, Baldisseri, Elena, Olioso, Debora, Duca, Martina, Tedesco, Erika, Leo, Sara, Borgatti, Monica, Volpi, Sonia, Pinton, Paolo, Cabrini, Giulio, Gambari, Roberto, Blasi, Francesco, Lippi, Giuseppe, Rimessi, Alessandro, Rizzo, Roberta, Cipolli, Marco

“…As an inherited disorder characterized by severe pulmonary disease, cystic fibrosis could be considered a comorbidity for coronavirus disease 2019. Instead,…”
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Use of mucoactive agents in cystic fibrosis: A consensus survey of Italian specialists by Volpi, Sonia, Carnovale, Vincenzo, Colombo, Carla, Raia, Valeria, Blasi, Francesco, Pappagallo, Giovanni

“…Background The goal of mucoactive therapies in cystic fibrosis (CF) is to enhance sputum clearance and to reduce a progressive decline in lung function over…”
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Toothbrushes may convey bacteria to the cystic fibrosis lower airways by Passarelli Mantovani, Rebeca, Sandri, Angela, Boaretti, Marzia, Grilli, Alessandra, Volpi, Sonia, Melotti, Paola, Burlacchini, Gloria, Lleò, Maria M., Signoretto, Caterina

“…Recent findings indicate that the oral cavity acts as a bacterial reservoir and might contribute to the transmission of bacteria to the lower airways. Control…”
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Relationship Between Lung Volumes and Heterogeneity in the Response to Elexacaftor/Tezacaftor/Ivacaftor in Patients With Cystic Fibrosis and Advanced Lung Disease by Gramegna, Andrea, Alicandro, Gianfranco, Premuda, Chiara, Lucca, Francesca, Pinali, Lucia, Retucci, Mariangela, Vespro, Valentina, Andrisani, Maria Carmela, Carraffiello, Gianpaolo, Amati, Francesco, Volpi, Sonia, Aliberti, Stefano, Cipolli, Marco, Blasi, Francesco

“…The effects of elexacaftor/tezacaftor/ivacaftor (ETI) on respiratory outcomes for people with cystic fibrosis (CF) were demonstrated by several clinical…”
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A longitudinal study of glucose tolerance in cystic fibrosis: the central role of beta cell functional mass by Piona, Claudia, Mozzillo, Enza, Tosco, Antonella, Zusi, Chiara, Emiliani, Federica, Volpi, Sonia, Di Candia, Francesca, Raia, Valeria, Boselli, Maria Linda, Trombetta, Maddalena, Cipolli, Marco, Bonadonna, Riccardo C, Maffeis, Claudio

“…The pathophysiological mechanisms underlying the natural history of glucose intolerance and its fluctuations in subjects with cystic fibrosis (CF) are still…”
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Delayed age at menarche in chronic respiratory diseases by Gaudino, Rossella, Dal Ben, Sarah, Cavarzere, Paolo, Volpi, Sonia, Piona, Claudia, Boner, Attilio, Antoniazzi, Franco, Piacentini, Giorgio

“…Objective Age at menarche (AAM) is an important indicator of physiological development in women, and delayed AAM has been associated with chronic illnesses. We…”
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Long-term clinical outcomes of elexacaftor/tezacaftor/ivacaftor therapy in adults with cystic fibrosis and advanced pulmonary disease by Savi, Daniela, Lucca, Francesca, Tridello, Gloria, Meneghelli, Ilaria, Comello, Isabella, Tomezzoli, Sara, Signorini, Monica, Proietti, Elena, Cucchetto, Giulia, Volpi, Sonia, Cipolli, Marco

“…The combination of cystic fibrosis transmembrane conductance regulator (CFTR) modulators elexacaftor, tezacaftor and ivacaftor (ELX/TEZ/IVA) has been approved…”
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Glucose Tolerance Stages in Cystic Fibrosis Are Identified by a Unique Pattern of Defects of Beta-Cell Function by Piona, Claudia, Volpi, Sonia, Zusi, Chiara, Mozzillo, Enza, Tosco, Antonella, Franzese, Adriana, Raia, Valeria, Boselli, Maria Linda, Trombetta, Maddalena, Cipolli, Marco, Bonadonna, Riccardo C, Maffeis, Claudio

“…Abstract Objective We aimed to assess the order of severity of the defects of 3 direct determinants of glucose regulation—beta-cell function, insulin…”
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The non-invasive evaluation of vascular liver disease in patients with cystic fibrosis: a prospective cross-sectional study by Dajti, Elton, Ravaioli, Federico, Paiola, Giulia, Volpi, Sonia, Colecchia, Luigi, Ferrarese, Alberto, Alemanni, Luigina Vanessa, Cusumano, Caterina, Di Biase, Annarita, Marasco, Giovanni, Vestito, Amanda, Festi, Davide, Rautou, Pierre-Emmanuel, Cipolli, Marco, Colecchia, Antonio

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THU-293 - The non-invasive evaluation of vascular liver disease in patients with cystic fibrosis: a prospective cross-sectional study by Dajti, Elton, Ravaioli, Federico, Paiola, Giulia, Volpi, Sonia, Colecchia, Luigi, Ferrarese, Alberto, Alemanni, Luigina Vanessa, Cusumano, Caterina, Di Biase, Annarita, Marasco, Giovanni, Vestito, Amanda, Festi, Davide, Rautou, Pierre-Emmanuel, Cipolli, Marco, Colecchia, Antonio

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Inconclusive diagnosis of cystic fibrosis after newborn screening by Ooi, Chee Y, Castellani, Carlo, Keenan, Katherine, Avolio, Julie, Volpi, Sonia, Boland, Margaret, Kovesi, Tom, Bjornson, Candice, Chilvers, Mark A, Morgan, Lenna, van Wylick, Richard, Kent, Steven, Price, April, Solomon, Melinda, Tam, Karen, Taylor, Louise, Malitt, Kylie-Ann, Ratjen, Felix, Durie, Peter R, Gonska, Tanja

“…To prospectively study infants with an inconclusive diagnosis of cystic fibrosis (CF) identified by newborn screening (NBS; "CF screen positive, inconclusive…”
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The non‐invasive evaluation of liver involvement in patients with cystic fibrosis: A prospective study by Dajti, Elton, Ravaioli, Federico, Paiola, Giulia, Volpi, Sonia, Colecchia, Luigi, Ferrarese, Alberto, Alemanni, Luigina Vanessa, Cusumano, Caterina, Di Biase, Anna Rita, Marasco, Giovanni, Vestito, Amanda, Festi, Davide, Rautou, Pierre‐Emmanuel, Cipolli, Marco, Colecchia, Antonio

“…Background and AimsPorto‐sinusoidal vascular disease (PSVD) has been described as the prominent pathology in liver explants of patients with cystic fibrosis…”
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Age at menarche in girls with cystic fibrosis and asthma by Dal Ben, Sarah, Gaudino, Rossella, Cavarzere, Paolo, Volpi, Sonia, Antoniazzi, Franco, Boner, Attilio, Piacentini, Giorgio

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The effect of inhaled hypertonic saline on lung structure in children aged 3–6 years with cystic fibrosis (SHIP-CT): a multicentre, randomised, double-blind, controlled trial by Tiddens, Harm A W M, Chen, Yuxin, Andrinopoulou, Eleni-Rosalina, Davis, Stephanie D, Rosenfeld, Margaret, Ratjen, Felix, Kronmal, Richard A, Hinckley Stukovsky, Karen D, Dasiewicz, Alison, Stick, Stephen Michael, Andrinopoulou, Eleni-Rosalina, Anthony, Margaret M., Au, Jacky, Belessis, Yvonne, Bonte, Merlijn, Chen, Yuxin, Cheney, Joyce, Clem, Charles, Clements, Barry, Cooper, Peter, Dasiewicz, Alison, Davis, Stephanie D., Davis, Miriam, de Boeck, Kris, de Marchis, Matteo, De Wachter, Elke, Delaisi, Bertrand, Delaup, Véronique, DeRicco, Adrienne, Foti, Alexia, Gan, Richard, Garriga, Laura, Gartner, Silvia, Genatossio, Alan, Grogan, Sam, Hilton, Jodi, Hinckley Stukovsky, Karen D, Hoppe, Jordana E., Janssens, Hettie M., Jensen, Renee, Johnson, Robin, Kemner-van de Corput, Mariette P.C., Klein, Brendan, Kronmal, Richard A., Lucca, Francesca, Lucidi, Vincencina, Montemitro, Enza, Nahidi, Lily, Nielsen, Kim G., Pearce, Kasey, Pittman, Jessica E, Powers, Michael, Prentice, Carley, Pressler, Tania, Ratjen, Felix, Rayment, Jonathan H, Reix, Philippe, Retsch-Bogart, George, Riera, Luis, Robinson, Phil, Robinson, Paul, Rosenfeld, Margaret, Sanders, Don B., Sandoval, Rodrigo A., Sandvik, Rikke Mulvad, Saunders, Clare, Siegel, Molly, Smith, Julie, Solomon, Melinda, Stanojevic, Sanja, Stick, Stephen Michael, Tai, Andrew, Tiddens, Harm A.W.M., van de Puttelaar, Jorien, Van den Brande, Christel, van Straten, Marcel, Vermeulen, Francois, Volpi, Sonia, Wainwright, Claire E., Weiner, Daniel J., Yuan, Yi, Zaimeddine, Sarah

“…In the Saline Hypertonic in Preschoolers (SHIP) study, inhaled 7% hypertonic saline improved the lung clearance index in children aged 3–6 years with cystic…”
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Impact of CFTR Modulators on Beta-Cell Function in Children and Young Adults with Cystic Fibrosis by Piona, Claudia, Mozzillo, Enza, Tosco, Antonella, Volpi, Sonia, Rosanio, Francesco Maria, Cimbalo, Chiara, Franzese, Adriana, Raia, Valeria, Zusi, Chiara, Emiliani, Federica, Boselli, Maria Linda, Trombetta, Maddalena, Bonadonna, Riccardo Crocina, Cipolli, Marco, Maffeis, Claudio

“…Background: To date, no consistent data are available on the possible impact of CFTR modulators on glucose metabolism. The aim of this study was to test the…”
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Lung function comparison between two decades in cystic fibrosis children: A single centre study by Tridello, Gloria, Volpi, Sonia, Assael, Baroukh M., Meneghelli, Ilaria, Passiu, Marianna, Circelli, Maria

“…Summary Objectives The purpose of this study was to compare two cohorts of cystic fibrosis (CF) patients born and treated in two different decades, diagnosed…”
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Lung function comparison between two decades in cystic fibrosis children: A single centre study: A Cohort Effect of Lung Function in CF Children by Tridello, Gloria, Volpi, Sonia, Assael, Baroukh M., Meneghelli, Ilaria, Passiu, Marianna, Circelli, Maria

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Growth and long-term lung function in cystic fibrosis: A longitudinal study of patients diagnosed by neonatal screening by Assael, Baroukh Maurice, Casazza, Giovanni, Iansa, Patrizia, Volpi, Sonia, Milani, Silvano

“…Objective So far there is no long‐term analysis relating the achievement of growth milestones (such as prepubertal and pubertal take‐off and peak velocity) to…”
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In silico analysis and theratyping of an ultra-rare CFTR genotype (W57G/A234D) in primary human rectal and nasal epithelial cells by Kleinfelder, Karina, Lotti, Virginia, Eramo, Adriana, Amato, Felice, Lo Cicero, Stefania, Castelli, Germana, Spadaro, Francesca, Farinazzo, Alessia, Dell’Orco, Daniele, Preato, Sara, Conti, Jessica, Rodella, Luca, Tomba, Francesco, Cerofolini, Angelo, Baldisseri, Elena, Bertini, Marina, Volpi, Sonia, Villella, Valeria Rachela, Esposito, Speranza, Zollo, Immacolata, Castaldo, Giuseppe, Laudanna, Carlo, Sorsher, Eric J., Hong, Jeong, Joshi, Disha, Cutting, Garry, Lucarelli, Marco, Melotti, Paola, Sorio, Claudio

“…Mutation targeted therapy in cystic fibrosis (CF) is still not eligible for all CF subjects, especially for cases carrying rare variants such as the CFTR…”
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