More articles from Cystic fibrosis

Lung Clearance Index (LCI) derived from N2-Multiple Breath Washout (MBW) depicts worsening in airways colonization in pediatric Cystic Fibrosis (CF) patients (pts)
Francesca Lucca, Sonia Volpi, Antonella Borruso, Laura Menin, Emily Pintani, Marco Cipolli

European Respiratory Journal Sep 2020, 56 (suppl 64) 354; DOI: 10.1183/13993003.congress-2020.354
Sleep duration and activity of exacerbated and non-exacerbated cystic fibrosis patients during their hospital stay
Carolin-Maria Linker, Svenja Straßburg, Sarah Dietz-Terjung, Matthias Welsner, Sebastian Brato, Christian Taube, Christoph Schöbel, Jürgen Götze, Gerhard Weinreich

European Respiratory Journal Sep 2020, 56 (suppl 64) 360; DOI: 10.1183/13993003.congress-2020.360
European Cystic Fibrosis Society Clinical Trials Network (ECFS-CTN): structure and impact since 2009
Silke Van Koningsbruggen-Rietschel, Damian G. Downey, Lieven Dupont, Fiona Dunlevy, Veerle Bulteel, Kate Hayes, Nick Simmonds, Nadine Dufeu, Hettie M. Janssens, Dorota Sands, Paola De Carli, Isabelle Sermet-Gaudelus, Kris De Boeck, Tim Lee, Isabelle Fajac

European Respiratory Journal Sep 2020, 56 (suppl 64) 367; DOI: 10.1183/13993003.congress-2020.367
Rescue of CFTR function impaired by mutations in exon 15
Kelly Martinovich, Anthony Kicic, Sue Fletcher, Steve Wilton, Steve Stick

European Respiratory Journal Sep 2020, 56 (suppl 64) 361; DOI: 10.1183/13993003.congress-2020.361
Vitamin D status correlates with lung function in children and adolescents with cystic fibrosis
Elena Zhekaite, Elena Kondratyeva, Anna Voronkova, Viktoria Sherman, Roman Budzinsky, Aisa Zodbinova, Yulia Melyanovskaya

European Respiratory Journal Sep 2020, 56 (suppl 64) 366; DOI: 10.1183/13993003.congress-2020.366
Blood gas analysis to predict survival in patients with cystic fibrosis
Johanna Manuela Kurz, Ben Spycher, Romy Rodriguez, Reta Fischer Biner, Philipp Latzin, Florian Singer

European Respiratory Journal Sep 2020, 56 (suppl 64) 358; DOI: 10.1183/13993003.congress-2020.358
Is Pulmonary Medication Adherence affected by disease severity among adult patients with Cystic Fibrosis?
Elpis Hatziagorou, Katerina Manika, S.S. Kyrvasili, E Kouroukli, E Sourla, I Lialias, S.C. Kotoulas, M Sionidou, J Kioumis, J Tsanakas

European Respiratory Journal Sep 2020, 56 (suppl 64) 368; DOI: 10.1183/13993003.congress-2020.368
Shedding light into the black box of infant multiple-breath washout
Marc-Alexander Oestreich, Florian Wyler, Philipp Latzin, Kathryn Ramsey

European Respiratory Journal Sep 2020, 56 (suppl 64) 355; DOI: 10.1183/13993003.congress-2020.355
Electrical impedance tomography as a clinical monitoring tool in patients with cystic fibrosis
Anna Folino, Sheila Beux, Laura Barrocu, Irene Esposito, Benedetta Crida, Roberta Cotti, Lorenzo Appendini, Elisabetta Bignamini

European Respiratory Journal Sep 2020, 56 (suppl 64) 352; DOI: 10.1183/13993003.congress-2020.352
Electronic nose (E-nose) analysis of exhaled volatile organic compounds (VOCs) distinguishes pediatric patients (pts) with Cystic fibrosis (CF) from healthy controls (HC) and depicts disease status
Francesca Lucca, Sonia Volpi, Laura Tenero, Michele Piazza, Marco Sandri, Marco Cipolli, Giorgio Piacentini

European Respiratory Journal Sep 2020, 56 (suppl 64) 353; DOI: 10.1183/13993003.congress-2020.353

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