Zobrazeno 1 - 10
of 12
pro vyhledávání: '"C H M van Moorsel"'
Autor:
M. C. Schimmelpennink, D. B. Meek, A. D. M. Vorselaars, L. C. M. Langezaal, C. H. M. van Moorsel, J. J. van der Vis, M. Veltkamp, J. C. Grutters
Publikováno v:
Respiratory Research, Vol 23, Iss 1, Pp 1-10 (2022)
Abstract Background Advanced pulmonary sarcoidosis causes significant morbidity and can lead to death. Large trials demonstrated efficacy of antifibrotics in patients with progressive fibrosing interstitial lung diseases (PF-ILD), including a few wit
Externí odkaz:
https://doaj.org/article/c46a96ad0a0948658b14e8264ff2d4c3
Autor:
Douwe H. Biesma, Karin M. Kazemier, C H M van Moorsel, Jan C. Grutters, D.A. van Kessel, Thijs W. Hoffman
Publikováno v:
Lung. 199:667-676
Idiopathic pulmonary fibrosis (IPF) is a severe fibrotic lung disease, in which inflammation is thought to only play a secondary role. Several factors associated with acute exacerbations of IPF (AE-IPF) have been identified, including infections. Thi
Autor:
T. W. Hoffman, J. J. van der Vis, M. F. M. van Oosterhout, H. W. van Es, D. A. van Kessel, J. C. Grutters, C. H. M. van Moorsel
Publikováno v:
Case Reports in Pulmonology, Vol 2016 (2016)
Pulmonary fibrosis is a frequent manifestation of telomere syndromes. Telomere gene mutations are found in up to 25% and 3% of patients with familial disease and sporadic disease, respectively. The telomere gene TINF2 encodes an eponymous protein tha
Externí odkaz:
https://doaj.org/article/067f5a2eeeb44ab2a8442efe030ab1dd
Publikováno v:
Lung. 199(6)
Idiopathic pulmonary fibrosis (IPF) is a severe fibrotic lung disease, in which inflammation is thought to only play a secondary role. Several factors associated with acute exacerbations of IPF (AE-IPF) have been identified, including infections. Thi
Publikováno v:
Respiratory Medicine. 194:106760
Patients with progressive fibrosing interstitial lung disease (PF-ILD) are prone to early mortality compared with other phenotypes of ILD. The possible effect of smoking on survival has not been investigated yet. Furthermore, it is unknown what the e
Autor:
Jan C. Grutters, Anouk Verwoerd, Anke M.E. Claessen, C H M van Moorsel, A D M Vorselaars, Daniëlle Hijdra, Heleen A. Crommelin
Publikováno v:
Clinical and Experimental Immunology, 185(2), 263. Wiley-Blackwell
Summary Sarcoidosis is a systemic granulomatous disease of unknown aetiology that most commonly affects the lungs. Although elevated levels of regulatory T cells (Tregs) have been reported, the extent to which they play a role in sarcoidosis pathogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::662daf580d0920b428107095da512511
https://dspace.library.uu.nl/handle/1874/345369
https://dspace.library.uu.nl/handle/1874/345369
Autor:
F.W. Welter-Schultes, Martin Haase, C. H. M. van Moorsel, E.W. Gutteling, Menno Schilthuizen, Edmund Gittenberger
Publikováno v:
Biological Journal of the Linnean Society. 83:317-326
The polytypic Cretan land snail Albinaria hippolyti has a range that is partly fragmented and partly subdivided by hybrid zones. For this reason, it has served as a model species for investigating speciation and radiation in Mediterranean Clausiliida
Publikováno v:
Journal of Molluscan Studies. 66:570-573
The ensuing contribution gives an insight into the evolution of non-coding ribosomal DNA of two distantly related groups of snails. The non-coding sequences of the ribosomal DNA comprise the First Internal Transcribed Spacer (ITS-1), the Second Inter
Autor:
E A, Kastelijn, C H M, van Moorsel, H J T, Ruven, N M, Korthagen, J M, Kwakkel-van Erp, E A, van de Graaf, P, Zanen, D A, van Kessel, J C, Grutters
Publikováno v:
Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG. 30(1)
The development of bronchiolitis obliterans syndrome (BOS) after lung transplantation is characterized by inflammation, remodeling and fibrosis. Both YKL-40 and matrix metalloproteinase (MMP)-9 have shown to be involved in these processes. We measure
Publikováno v:
Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG. 27(2)
Idiopathic pulmonary fibrosis (IPF) is a parenchymal lung disease characterized by progressive interstitial fibrosis. In 2002, the ATS/ERS published new criteria that significantly changed the definition of IPF, resulting in a more homogeneous group