Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Daan, Caudri"'
Autor:
Qianting Lv, Bernadette B.L.J. Elders, Adilia Warris, Daan Caudri, Pierluigi Ciet, Harm A.W.M. Tiddens
Publikováno v:
European Respiratory Review, Vol 30, Iss 162 (2021)
In people with cystic fibrosis (PwCF), viscous sputum and dysfunction of the mucociliary escalator leads to early and chronic infections. The prevalence of Aspergillus fumigatus in sputum is high in PwCF and the contribution of A. fumigatus to the pr
Externí odkaz:
https://doaj.org/article/45c0a685c72644ffb56ca42b59feac19
Autor:
Yuxin Chen, Qianting Lv, Eleni-Rosalina Andrinopoulou, Leticia Gallardo-Estrella, Jean-Paul Charbonnier, Daan Caudri, Stephanie D. Davis, Margaret Rosenfeld, Felix Ratjen, Richard A. Kronmal, Karen D. Hinckley Stukovsky, Stephen Stick, Harm A.W.M. Tiddens
Publikováno v:
Journal of Cystic Fibrosis. Elsevier
Background: SHIP-CT showed that 48-week treatment with inhaled 7% hypertonic saline (HS) reduced airway abnormalities on chest CT using the manual PRAGMA-CF method relative to isotonic saline (IS) in children aged 3-6 years with cystic fibrosis (CF).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::067ac4af1f1ff6cbeb4894cc424127ab
https://pure.eur.nl/en/publications/23ae9603-2f72-4d4d-b83d-9c57140b96fc
https://pure.eur.nl/en/publications/23ae9603-2f72-4d4d-b83d-9c57140b96fc
Autor:
Elaine Tham, Jenny Downs, Daan Caudri, Catherine S. Choong, Aleisha Nielsen, Gillian M. Nixon, Peter Jacoby, Andrew Wilson, Chris Seton, Claire Hafekost, Komal Vora, Charles F. Verge, Antony R Lafferty, Greg Blecher, Patricia Crock, Yassmin Musthaffa, Linda Mai, Nitin Kapur, Andrew Tai, Geoff Ambler, Philip Bergman
Publikováno v:
Journal of Paediatrics and Child Health, 58(2), 248-255. Wiley-Blackwell Publishing Ltd
Aim: In children with Prader-Willi syndrome (PWS), growth hormone (GH) improves height and body composition; however, may be associated with worsening sleep-disordered breathing (SDB). Some studies have reported less SDB after GH initiation, but foll
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c53e42d1f4c8de27e475ac25d71cb72b
https://pure.eur.nl/en/publications/736fce12-1ea8-43d2-af12-f1a426b943b8
https://pure.eur.nl/en/publications/736fce12-1ea8-43d2-af12-f1a426b943b8
Autor:
Nitin Kapur, Andrew Tai, Jenny Downs, Elaine Tham, Chris Seton, Yassmin Musthaffa, Peter Jacoby, Patricia Crock, Greg Blecher, Gillian M. Nixon, Charles F. Verge, Komal Vora, Antony R Lafferty, Cara Schofield, Andrew Wilson, Helen Leonard, Geoff Ambler, Philip Bergman, Daan Caudri, Catherine S. Choong, Jessica Mackay
Publikováno v:
Journal of Autism and Developmental Disorders, 52(9), 3877-3889. Springer New York
Prader-Willi syndrome (PWS) is a rare genetic disorder characterised by neurodevelopmental delays, hyperphagia, difficulties with social communication and challenging behaviours. Individuals require intensive supervision from caregivers which may neg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33b98a188b75e12ced8c13a7cd3754bf
https://pure.eur.nl/en/publications/219e78a3-1f63-4637-9cd1-e0c1562e0124
https://pure.eur.nl/en/publications/219e78a3-1f63-4637-9cd1-e0c1562e0124
Publikováno v:
Breathe, Vol 11, Iss 2, Pp 153-155 (2015)
Externí odkaz:
https://doaj.org/article/cddbf72fe6f94679bc86b5fb4cb205b3
Autor:
Sarath Ranganathan, Louise King, Alya Ishak, André Schultz, Stephen M. Stick, Daan Caudri, Lidija Turkovic, Peter D. Sly, Joanne Harrison
Publikováno v:
Chest, 158(6), 2314-2322. American College of Chest Physicians
Pulmonary exacerbations in cystic fibrosis are characterized by airway inflammation and may cause irreversible lung damage. Early identification of such exacerbations may facilitate early initiation of treatment, thereby potentially reducing long-ter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4999a8ea857a57c6f173cafda64156e
https://hdl.handle.net/1765/131910
https://hdl.handle.net/1765/131910
Autor:
Ferenc Karpati, L.E. Jenkins, D.M. Cox, Yvonne Belessis, Carla Federica Bortoluzzi, L. Da Dalt, Baroukh M. Assael, Ciro D'Orazio, Stéphanie Bui, V. Švabe, J.C. Dubus, L. Honková, A. Jung, Tanja Pressler, M. Geerdink, Phil Robinson, C. Vazquez, Rosaria Casciaro, Valeria Raia, A.J.M. Reid, C. Mainguy, Daan Caudri, Antonella Tosco, S. Rovira, M.C. Cavicchi, Eleonora Pontello, O. Sepe, Stephen M. Stick, A. Tai, Silvia Gartner, Paolo Rossi, M. G. Myriam Hunink, Veronika Skalická, Harm A.W.M. Tiddens, C.R. Hansen, A. Möller, Emily Pintani, Karin M. de Winter-de Groot, A.S. Neri, E. Rietschel, André Schultz, F. De Gregorio, Marijke Proesmans, F. Bremont, Paul Robinson
Publikováno v:
Journal of Cystic Fibrosis, 19(4), 641-646. Elsevier
Background Recent standards of care mention chest radiography (CR) but not chest computed tomography (CT) in routine annual follow-up of children with cystic fibrosis (CF). To minimise radiation risk, CT or CR should only be performed if they impact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ebbc725b4af89aebcda619690db28c4
https://doi.org/10.1016/j.jcf.2019.08.005
https://doi.org/10.1016/j.jcf.2019.08.005
Autor:
Peter D. Sly, Sarath Ranganathan, André Schultz, Lauren S. Akesson, Stephen M. Stick, Luke W. Garratt, Lidija Turkovic, Daan Caudri, Oded Breuer, Tim Rosenow, Conor P Murray, Yuliya V. Karpievitch, Samuel Dalton
Publikováno v:
American Journal of Respiratory and Critical Care Medicine, 201, 688-696. American Thoracic Society
Rationale: Recent data show that Aspergillus species are prevalent respiratory infections in children with cystic fibrosis (CF). The biological significance of these infections is unknown.Objective...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67d51a4b2b28047b225e381ebf5c6d1e
https://pure.eur.nl/en/publications/a1fe16cc-7245-427a-95e0-d2e2ca0982fc
https://pure.eur.nl/en/publications/a1fe16cc-7245-427a-95e0-d2e2ca0982fc
Autor:
Lidija Turkovic, Nicholas de Klerk, Oded Breuer, Tim Rosenow, Conor Murray, Ewout W. Steyerberg, Sarath Ranganathan, Daan Caudri, Stephen M. Stick, Peter D. Sly
Publikováno v:
Pediatric Pulmonology, 57(1), 122-131. Wiley-Liss Inc.
Pediatric Pulmonology, 57(1), 122-131. WILEY
Pediatric Pulmonology, 57(1), 122-131. WILEY
Background: The marked heterogeneity in cystic fibrosis (CF) disease complicates the selection of those most likely to benefit from existing or emergent treatments. Objective: We aimed to predict the progression of bronchiectasis in preschool childre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d93349d1b8c41f29abc8c9cbab474ff4
https://hdl.handle.net/1887/3564486
https://hdl.handle.net/1887/3564486
Autor:
Daan Caudri, Lidija Turkovic, Nicholas de Klerk, Tim Rosenow, Conor Murray, Ewout Steyerberg, Sarath Ranganathan, Peter Sly, Stephen Stick, Oded Breuer
Background: The marked heterogeneity in CF disease complicates selection of those most likely to benefit from existing or emergent treatments. Objective: We aimed to predict progression of bronchiectasis in preschool children with CF. Methods: Using
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28c85d4a004aba3c906b4a245e166094
https://doi.org/10.22541/au.162265771.16822186/v1
https://doi.org/10.22541/au.162265771.16822186/v1