Zobrazeno 1 - 10
of 114
pro vyhledávání: '"Eric G. Haarman"'
Autor:
Yin Ting Lam, Jean-François Papon, Mihaela Alexandru, Andreas Anagiotos, Miguel Armengot, Mieke Boon, Andrea Burgess, Nathalie Caversaccio, Suzanne Crowley, Sinan Ahmed D. Dheyauldeen, Nagehan Emiralioglu, Ela Erdem, Christine van Gogh, Yasemin Gokdemir, Onder Gunaydın, Eric G. Haarman, Amanda Harris, Isolde Hayn, Hasnaa Ismail-Koch, Bulent Karadag, Céline Kempeneers, Sookyung Kim, Natalie Lorent, Ugur Ozcelik, Charlotte Pioch, Anne-Lise ML Poirrier, Ana Reula, Jobst Roehmel, Panayiotis Yiallouros, Myrofora Goutaki
Publikováno v:
Clinical and Experimental Otorhinolaryngology, Vol 16, Iss 4, Pp 407-412 (2023)
Externí odkaz:
https://doaj.org/article/b2b677241c6f446290767afbff9355b3
Autor:
Renate Kos, Myrofora Goutaki, Helene E. Kobbernagel, Bruna Rubbo, Amelia Shoemark, Stefano Aliberti, Josje Altenburg, Pinelopi Anagnostopoulou, Rodrigo A. Athanazio, Nicole Beydon, Sharon D. Dell, Nagehan Emiralioglu, Thomas W. Ferkol, Michael R. Loebinger, Natalie Lorent, Bernard Maître, June Marthin, Lucy C. Morgan, Kim G. Nielsen, Felix C. Ringshausen, Michal Shteinberg, Harm A.W.M. Tiddens, Anke H. Maitland-Van der Zee, James D. Chalmers, Jane S.A. Lucas, Eric G. Haarman
Publikováno v:
ERJ Open Research, Vol 10, Iss 1 (2024)
Background Consistent use of reliable and clinically appropriate outcome measures is a priority for clinical trials, with clear definitions to allow comparability. We aimed to develop a core outcome set (COS) for pulmonary disease interventions in pr
Externí odkaz:
https://doaj.org/article/206a1713eedc40ba92a771037176fcd8
Autor:
Yin Ting Lam, Jean-François Papon, Mihaela Alexandru, Andreas Anagiotos, Miguel Armengot, Mieke Boon, Andrea Burgess, Suzanne Crowley, Sinan Ahmed D. Dheyauldeen, Nagehan Emiralioglu, Ela Erdem Eralp, Christine van Gogh, Yasemin Gokdemir, Onder Gunaydın, Eric G. Haarman, Amanda Harris, Isolde Hayn, Hasnaa Ismail-Koch, Bülent Karadag, Céline Kempeneers, Sookyung Kim, Philipp Latzin, Natalie Lorent, Ugur Ozcelik, Charlotte Pioch, Anne-Lise M.L. Poirrier, Ana Reula, Jobst Roehmel, Panayiotis Yiallouros, on behalf of the EPIC-PCD team, Myrofora Goutaki
Publikováno v:
ERJ Open Research, Vol 9, Iss 3 (2023)
Background Sinonasal symptoms are a common feature of primary ciliary dyskinesia (PCD); however, literature about their severity and frequency, particularly during the life course, is scarce. Using baseline data from the Ear, nose and throat (ENT) Pr
Externí odkaz:
https://doaj.org/article/af2659ccbe26408ba0bf123c0d1ed6c3
Autor:
Renate Kos, Anne H. Neerincx, Dominic W. Fenn, Paul Brinkman, Rianne Lub, Steffie E. M. Vonk, Jolt Roukema, Monique H. Reijers, Suzanne W. J. Terheggen‐Lagro, Josje Altenburg, Christof J. Majoor, Lieuwe D. Bos, Eric G. Haarman, Anke H. Maitland‐van der Zee, the Amsterdam Mucociliary Clearance Disease (AMCD) Research Group
Publikováno v:
Pharmacology Research & Perspectives, Vol 10, Iss 6, Pp n/a-n/a (2022)
Abstract Elexacaftor/tezacaftor/ivacaftor (ETI) is a cystic fibrosis (CF) transmembrane conductance regulator modulator, which has shown efficacy in CF patients (≥6 years) with ≥1 Phe508del mutation and a minimal function mutation. In October 201
Externí odkaz:
https://doaj.org/article/61e4264a25824ffe91e5cce2222b9fea
Autor:
Henriette H. M. Dreyer, Eleonora Sofie van Tuyll van Serooskerken, Lisa W. Rodenburg, Arnold J. N. Bittermann, Hubertus G. M. Arets, Ellen M. B. P. Reuling, Johannes W. Verweij, Eric G. Haarman, David C. van der Zee, Stefaan H. A. J. Tytgat, Cornelis K. van der Ent, Jeffrey M. Beekman, Gimano D. Amatngalim, Maud Y. A. Lindeboom
Publikováno v:
Children, Vol 10, Iss 6, p 1020 (2023)
Esophageal atresia (EA) is a rare birth defect in which respiratory tract disorders are a major cause of morbidity. It remains unclear whether respiratory tract disorders are in part caused by alterations in airway epithelial cell functions such as t
Externí odkaz:
https://doaj.org/article/49357c20bf05479cb1c93c1c52b71d08
Autor:
Johanna Raidt, Bernard Maitre, Petra Pennekamp, Josje Altenburg, Pinelopi Anagnostopoulou, Miguel Armengot, Lizan D. Bloemsma, Mieke Boon, Melissa Borrelli, Folke Brinkmann, Siobhan B. Carr, Mary P. Carroll, Silvia Castillo-Corullón, André Coste, Renato Cutrera, Eleonora Dehlink, Damien M.S. Destouches, Maria E. Di Cicco, Lucy Dixon, Nagehan Emiralioglu, Ela Erdem Eralp, Eric G. Haarman, Claire Hogg, Bulent Karadag, Helene E. Kobbernagel, Natalie Lorent, Marcus A. Mall, June K. Marthin, Vendula Martinu, Manjith Narayanan, Ugur Ozcelik, Daniel Peckham, Massimo Pifferi, Petr Pohunek, Eva Polverino, Simon Range, Felix C. Ringshausen, Evie Robson, Jobst Roehmel, Sandra Rovira-Amigo, Francesca Santamaria, Anne Schlegtendal, Zsolt Szépfalusi, Petra Tempels, Guillaume Thouvenin, Nicola Ullmann, Woolf T. Walker, Martin Wetzke, Panayiotis Yiallouros, Heymut Omran, Kim G. Nielsen
Publikováno v:
ERJ Open Research, Vol 8, Iss 3 (2022)
Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterised by impaired mucociliary clearance leading to irreversible lung damage. In contrast to other rare lung diseases like cystic fibrosis (CF), there are only few clinical trials and
Externí odkaz:
https://doaj.org/article/71c85d757d254e3f8fc3ac7e15aee183
Rituximab in Idiopathic Pulmonary Hemosiderosis in Children: A Novel and Less Toxic Treatment Option
Autor:
Suzanne W. J. Terheggen-Lagro, Eric G. Haarman, Niels W. Rutjes, J. Merlijn van den Berg, Dieneke Schonenberg-Meinema
Publikováno v:
Pharmaceuticals, Vol 15, Iss 12, p 1549 (2022)
Idiopathic pulmonary hemosiderosis (IPH) is a rare, potentially life-threatening chronic disease. Steroids are the cornerstone of treatment, even though toxicity and side-effects are very common. Recently, rituximab (RTX) has been suggested as a trea
Externí odkaz:
https://doaj.org/article/0f434a4dfb9844c5b7ae2a4b76a1fbc0
Autor:
Panayiotis Kouis, Myrofora Goutaki, Florian S. Halbeisen, Ifigeneia Gioti, Nicos Middleton, Israel Amirav, on behalf of the Israeli PCD Consortium, Angelo Barbato, on behalf of the Italian PCD Consortium, Laura Behan, Mieke Boon, Nagehan Emiralioglu, Eric G. Haarman, Bulent Karadag, Cordula Koerner-Rettberg, Romain Lazor, on behalf of the Swiss PCD Group, Michael R. Loebinger, Bernard Maitre, on behalf of the French Reference Centre for Rare Lung Diseases, Henryk Mazurek, Lucy Morgan, Kim Gjerum Nielsen, Heymut Omran, Ugur Özçelik, Mareike Price, Andrzej Pogorzelski, Deborah Snijders, on behalf of the PCD Italian Consortium, Guillaume Thouvenin, Claudius Werner, Zorica Zivkovic, Claudia E. Kuehni, Panayiotis K. Yiallouros
Publikováno v:
Respiratory Research, Vol 20, Iss 1, Pp 1-12 (2019)
Abstract Background Lung resection is a controversial and understudied therapeutic modality in Primary Ciliary Dyskinesia (PCD). We assessed the prevalence of lung resection in PCD across countries and compared disease course in lobectomised and non-
Externí odkaz:
https://doaj.org/article/c428f64b0b3e41d1a14ad10bef7262ea
Autor:
Job J.M.H. van Bragt, Paul Brinkman, Rianne de Vries, Susanne J.H. Vijverberg, Els J.M. Weersink, Eric G. Haarman, Frans H.C. de Jongh, Sigrid Kester, Annelies Lucas, Johannes C.C.M. in 't Veen, Peter J. Sterk, Elisabeth H.D. Bel, Anke H. Maitland-van der Zee
Publikováno v:
ERJ Open Research, Vol 6, Iss 4 (2020)
Molecular profiling of exhaled breath by electronic nose (eNose) might be suitable as a noninvasive tool that can help in monitoring of clinically unstable COPD patients. However, supporting data are still lacking. Therefore, as a first step, this st
Externí odkaz:
https://doaj.org/article/c7ce607d47cb4c43b5ee15e6c9274687
Autor:
Valentina Ferraro, Eleni-Rosalina Andrinopoulou, Anna Marthe Margaretha Sijbring, Eric G. Haarman, Harm A.W.M. Tiddens, Marielle W.H. Pijnenburg
Publikováno v:
ERJ Open Research, Vol 6, Iss 3 (2020)
Chest computed tomography (CT) is the gold standard for detecting structural abnormalities in patients with primary ciliary dyskinesia (PCD) such as bronchiectasis, bronchial wall thickening and mucus plugging. There are no studies on quantitative as
Externí odkaz:
https://doaj.org/article/f85a6e3ce8284c92904d58b7afab2d38