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6 results on '"Gartner, Silvia"'

2. Cystic Fibrosis Cases Missed by Newborn Bloodspot Screening—Towards a Consistent Definition and Data Acquisition

Author

Munck, Anne, primary, Southern, Kevin W., additional, Murphy, Jared, additional, de Winter-de Groot, Karin M., additional, Gartner, Silvia, additional, Karadag, Bülent, additional, Kashirskaya, Nataliya, additional, Linnane, Barry, additional, Proesmans, Marijke, additional, Sands, Dorota, additional, Sommerburg, Olaf, additional, Castellani, Carlo, additional, and Barben, Jürg, additional

Published
2023
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3. The Management of Asymptomatic Congenital Pulmonary Airway Malformation: Results of a European Delphi Survey

Author

Kersten, Casper M., primary, Hermelijn, Sergei M., additional, Mullassery, Dhanya, additional, Muthialu, Nagarajan, additional, Cobanoglu, Nazan, additional, Gartner, Silvia, additional, Bagolan, Pietro, additional, Mesas Burgos, Carmen, additional, Sgrò, Alberto, additional, Heyman, Stijn, additional, Till, Holger, additional, Suominen, Janne, additional, Schurink, Maarten, additional, Desender, Liesbeth, additional, Losty, Paul, additional, Steyaert, Henri, additional, Terheggen-Lagro, Suzanne, additional, Metzelder, Martin, additional, Bonnard, Arnaud, additional, Sfeir, Rony, additional, Singh, Michael, additional, Yardley, Iain, additional, Rikkers-Mutsaerts, Noor R. V. M., additional, van der Ent, Cornelis K., additional, Qvist, Niels, additional, Cox, Des W., additional, Peters, Robert, additional, Bannier, Michiel A. G. E., additional, Wessel, Lucas, additional, Proesmans, Marijke, additional, Stanton, Michael, additional, Hannon, Edward, additional, Zampoli, Marco, additional, Morini, Francesco, additional, Tiddens, Harm A. W. M., additional, Wijnen, René M. H., additional, and Schnater, Johannes M., additional

Published
2022
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4. The Management of Asymptomatic Congenital Pulmonary Airway Malformation: Results of a European Delphi Survey

Author

Longziekten patientenzorg, Speerpunt Child Health, Child Health, Infection & Immunity, Kersten, Casper M., Hermelijn, Sergei M., Mullassery, Dhanya, Muthialu, Nagarajan, Cobanoglu, Nazan, Gartner, Silvia, Bagolan, Pietro, Mesas Burgos, Carmen, Sgrò, Alberto, Heyman, Stijn, Till, Holger, Suominen, Janne, Schurink, Maarten, Desender, Liesbeth, Losty, Paul, Steyaert, Henri, Terheggen-Lagro, Suzanne, Metzelder, Martin, Bonnard, Arnaud, Sfeir, Rony, Singh, Michael, Yardley, Iain, Rikkers-Mutsaerts, Noor R.V.M., van der Ent, Cornelis K., Qvist, Niels, Cox, Des W., Peters, Robert, Bannier, Michiel A.G.E., Wessel, Lucas, Proesmans, Marijke, Stanton, Michael, Hannon, Edward, Zampoli, Marco, Morini, Francesco, Tiddens, Harm A.W.M., Wijnen, René M.H., Schnater, Johannes M., Longziekten patientenzorg, Speerpunt Child Health, Child Health, Infection & Immunity, Kersten, Casper M., Hermelijn, Sergei M., Mullassery, Dhanya, Muthialu, Nagarajan, Cobanoglu, Nazan, Gartner, Silvia, Bagolan, Pietro, Mesas Burgos, Carmen, Sgrò, Alberto, Heyman, Stijn, Till, Holger, Suominen, Janne, Schurink, Maarten, Desender, Liesbeth, Losty, Paul, Steyaert, Henri, Terheggen-Lagro, Suzanne, Metzelder, Martin, Bonnard, Arnaud, Sfeir, Rony, Singh, Michael, Yardley, Iain, Rikkers-Mutsaerts, Noor R.V.M., van der Ent, Cornelis K., Qvist, Niels, Cox, Des W., Peters, Robert, Bannier, Michiel A.G.E., Wessel, Lucas, Proesmans, Marijke, Stanton, Michael, Hannon, Edward, Zampoli, Marco, Morini, Francesco, Tiddens, Harm A.W.M., Wijnen, René M.H., and Schnater, Johannes M.

Published
2022

5. Immunofluorescence Analysis as a Diagnostic Tool in a Spanish Cohort of Patients with Suspected Primary Ciliary Dyskinesia

Author

Baz-Redón, Noelia, primary, Rovira-Amigo, Sandra, additional, Fernández-Cancio, Mónica, additional, Castillo-Corullón, Silvia, additional, Cols, Maria, additional, Caballero-Rabasco, M. Araceli, additional, Asensio, Óscar, additional, Martín de Vicente, Carlos, additional, Martínez-Colls, Maria del Mar, additional, Torrent-Vernetta, Alba, additional, de Mir-Messa, Inés, additional, Gartner, Silvia, additional, Iglesias-Serrano, Ignacio, additional, Díez-Izquierdo, Ana, additional, Polverino, Eva, additional, Amengual-Pieras, Esther, additional, Amaro-Rodríguez, Rosanel, additional, Vendrell, Montserrat, additional, Mumany, Marta, additional, Pascual-Sánchez, María Teresa, additional, Pérez-Dueñas, Belén, additional, Reula, Ana, additional, Escribano, Amparo, additional, Dasí, Francisco, additional, Armengot-Carceller, Miguel, additional, Garrido-Pontnou, Marta, additional, Camats-Tarruella, Núria, additional, and Moreno-Galdó, Antonio, additional

Published
2020
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6. Elevated Prostaglandin E 2 Synthesis Is Associated with Clinical and Radiological Disease Severity in Cystic Fibrosis.

Author

Gartner S, Roca-Ferrer J, Fernandez-Alvarez P, Lima I, Rovira-Amigo S, García-Arumi E, Tizzano EF, and Picado C

Abstract

Background: Previous studies found high but very variable levels of tetranor-PGEM and PGDM (urine metabolites of prostaglandin (PG) E 2 and PGD 2 , respectively) in persons with cystic fibrosis (pwCF). This study aims to assess the role of cyclooxygenase COX-1 and COX-2 genetic polymorphisms in PG production and of PG metabolites as potential markers of symptoms' severity and imaging findings. Methods: A total of 30 healthy subjects and 103 pwCF were included in this study. Clinical and radiological CF severity was evaluated using clinical scoring methods and chest computed tomography (CT), respectively. Urine metabolites were measured using liquid chromatography/tandem mass spectrometry. Variants in the COX-1 gene (PTGS1 639 C>A, PTGS1 762+14delA and COX-2 gene: PTGS2-899G>C (-765G>C) and PTGS2 (8473T>C) were also analyzed. Results: PGE-M and PGD-M urine concentrations were significantly higher in pwCF than in controls. There were also statistically significant differences between clinically mild and moderate disease and severe disease. Patients with bronchiectasis and/or air trapping had higher PGE-M levels than patients without these complications. The four polymorphisms did not associate with clinical severity, air trapping, bronchiectasis, or urinary PG levels. Conclusions: These results suggest that urinary PG level testing can be used as a biomarker of CF severity. COX genetic polymorphisms are not involved in the variability of PG production.

Published
2024
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