Zobrazeno 1 - 10
of 266
pro vyhledávání: '"Wim A, Wuyts"'
Autor:
Lisa Lancaster, Vincent Cottin, Murali Ramaswamy, Wim A. Wuyts, R. Gisli Jenkins, Mary Beth Scholand, Michael Kreuter, Claudia Valenzuela, Christopher J. Ryerson, Jonathan Goldin, Grace Hyun J. Kim, Marzena Jurek, Martin Decaris, Annie Clark, Scott M. Turner, Chris N. Barnes, Hardean E. Achneck, Gregory P. Cosgrove, Éric A. Lefebvre, Kevin R. Flaherty
Publikováno v:
Therapeutic Advances in Respiratory Disease, Vol 18 (2024)
What is this summary about? This plain language summary shares results from a clinical study called INTEGRIS-IPF that was published in the American Journal of Respiratory and Critical Care Medicine in 2024. This study looked at a medicine called bexo
Externí odkaz:
https://doaj.org/article/d74c3c5acaf94d3797a66223b9ad603c
Autor:
Paul Ford, Michael Kreuter, Kevin K. Brown, Wim A. Wuyts, Marlies Wijsenbeek, Dominique Israël-Biet, Richard Hubbard, Steven D. Nathan, Hilario Nunes, Bjorn Penninckx, Niyati Prasad, Ineke Seghers, Paolo Spagnolo, Nadia Verbruggen, Nik Hirani, Juergen Behr, Robert J. Kaner, Toby M. Maher
Publikováno v:
ERJ Open Research, Vol 10, Iss 1 (2024)
Background There is no standard definition of respiratory-related hospitalisation, a common end-point in idiopathic pulmonary fibrosis (IPF) clinical trials. As diverse aetiologies and complicating comorbidities can present similarly, external adjudi
Externí odkaz:
https://doaj.org/article/dd10a57961ca4f14aca9968ef542372a
Autor:
Gizal Nakshbandi, Catharina C. Moor, Katerina Antoniou, Vincent Cottin, Anna-Maria Hoffmann-Vold, Edwin A. Koemans, Michael Kreuter, Philip L. Molyneaux, Wim A. Wuyts, Marlies S. Wijsenbeek
Publikováno v:
BMC Pulmonary Medicine, Vol 23, Iss 1, Pp 1-10 (2023)
Abstract Background Pulmonary fibrosis (PF) is caused by a heterogeneous group of diseases, with a high inter-individual variability in disease trajectory. Identifying disease progression in patients with PF has impact on clinical management decision
Externí odkaz:
https://doaj.org/article/208e2af0e837454b93041009cf411eb9
Autor:
Sandra Freitag-Wolf, Jonas C. Schupp, Björn C. Frye, Annegret Fischer, Raihanatul Anwar, Robert Kieszko, Violeta Mihailović-Vučinić, Janusz Milanowski, Dragana Jovanovic, Gernot Zissel, Elena Bargagli, Paola Rottoli, Dragos Bumbacea, René Jonkers, Ling-Pei Ho, Karoline I. Gaede, Anna Dubaniewicz, Ben G. Marshall, Andreas Günther, Martin Petrek, Michael P. Keane, Sigridur O. Haraldsdottir, Francesco Bonella, Christian Grah, Tatjana Peroš-Golubičić, Zamir Kadija, Stefan Pabst, Christian Grohé, János Strausz, Martina Safrankova, Ann Millar, Jiří Homolka, Wim A. Wuyts, Lisa G. Spencer, Michael Pfeifer, Dominique Valeyre, Venerino Poletti, Hubertus Wirtz, Antje Prasse, Stefan Schreiber, Astrid Dempfle, Joachim Müller-Quernheim
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
IntroductionSarcoidosis is a highly variable disease in terms of organ involvement, type of onset and course. Associations of genetic polymorphisms with sarcoidosis phenotypes have been observed and suggest genetic signatures.MethodsAfter obtaining a
Externí odkaz:
https://doaj.org/article/ad511b3d40084d7293d0e9577c3c3078
Autor:
Theodoros Karampitsakos, Phuong Phuong Diep, Daan W. Loth, Iftikhar Nadeem, Elene Khurtsidze, Marlies S. Wijsenbeek, Wim A. Wuyts, Elena Bargagli, Antoine Froidure, Paolo Spagnolo, Marcel Veltkamp, Maria Molina-Molina, Cormac McCarthy, Katerina M. Antoniou, Michael Kreuter, Catharina C. Moor
Publikováno v:
ERJ Open Research, Vol 9, Iss 2 (2023)
This article contains a selection of scientific highlights in the field of interstitial lung diseases (ILDs) presented at the hybrid European Respiratory Society International Congress 2022. Early Career Members of Assembly 12 summarise recent advanc
Externí odkaz:
https://doaj.org/article/60444a550cb94a2e93f6c54f5aa3d1a4
Autor:
Anouk Delameillieure, Fabienne Dobbels, Steffen Fieuws, Katleen Leceuvre, Sara Vanderauwera, Wim A. Wuyts
Publikováno v:
Respiratory Research, Vol 23, Iss 1, Pp 1-13 (2022)
Abstract Background Idiopathic pulmonary fibrosis (IPF) is a chronic and progressive lung condition. Currently, care models predominantly focus on acute medical and pharmacological needs. As a step towards holistic care, the aim of this prospective s
Externí odkaz:
https://doaj.org/article/99c8fe6d41b34b8a8f3dd3eb58376a64
Autor:
Michael Kreuter, Francesco Del Galdo, Corinna Miede, Dinesh Khanna, Wim A. Wuyts, Laura K. Hummers, Margarida Alves, Nils Schoof, Christian Stock, Yannick Allanore
Publikováno v:
Arthritis Research & Therapy, Vol 24, Iss 1, Pp 1-9 (2022)
Abstract Background Interstitial lung disease (ILD) is a common organ manifestation in systemic sclerosis (SSc) and is the leading cause of death in patients with SSc. A decline in forced vital capacity (FVC) is an indicator of ILD progression and is
Externí odkaz:
https://doaj.org/article/e3fd2be9ced043d2a49ee2bfb4b9b0f7
Autor:
Marie Vermant, Alexandros Kalkanis, Tinne Goos, Heleen Cypers, Nico De Crem, Barbara Neerinckx, Veerle Taelman, Patrick Verschueren, Wim A. Wuyts
Publikováno v:
Diagnostics, Vol 13, Iss 18, p 2986 (2023)
Background: Rheumatoid arthritis (RA) is a chronic auto-immune disease, typically affecting the joints, which can also present with lung involvement (pleuritis, interstitial lung disease, pulmonary nodules, etc.). Lung ultrasound (LUS) is an upcoming
Externí odkaz:
https://doaj.org/article/0bfa49b09f084b228324710f8314cbb8
Autor:
Steven Ronsmans, Jolien De Ridder, Eline Vandebroek, Stephan Keirsbilck, Benoit Nemery, Peter H. M. Hoet, Steven Vanderschueren, Wim A. Wuyts, Jonas Yserbyt
Publikováno v:
Respiratory Research, Vol 22, Iss 1, Pp 1-11 (2021)
Abstract Background Sarcoidosis most commonly affects lungs and intrathoracic lymph nodes, but any other organ can be involved. In epidemiological studies, many occupational and environmental exposures have been linked to sarcoidosis but their relati
Externí odkaz:
https://doaj.org/article/955afc69d414469e9d84fb2f4459174f
Autor:
Anouk Delameillieure, Sarah Vandekerkhof, Bastiaan Van Grootven, Wim A. Wuyts, Fabienne Dobbels
Publikováno v:
Respiratory Research, Vol 22, Iss 1, Pp 1-12 (2021)
Abstract Background The multidimensional and complex care needs of patients with idiopathic pulmonary fibrosis (IPF) call for appropriate care models. This systematic review aimed to identify care models or components thereof that have been developed
Externí odkaz:
https://doaj.org/article/a52a7c7d5be74cea87f1f5b44e0850db