Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Helene M. Schoemans"'
Autor:
Arno Vanstapel, Roel Goldschmeding, Roel Broekhuizen, Tri Nguyen, Annelore Sacreas, Janne Kaes, Tobias Heigl, Stijn E. Verleden, Alexandra De Zutter, Geert Verleden, Birgit Weynand, Erik Verbeken, Laurens J. Ceulemans, Dirk E. Van Raemdonck, Arne P. Neyrinck, Helene M. Schoemans, Bart M. Vanaudenaerde, Robin Vos
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
BackgroundConnective tissue growth factor (CTGF) is an important mediator in several fibrotic diseases, including lung fibrosis. We investigated CTGF-expression in chronic lung allograft dysfunction (CLAD) and pulmonary graft-versus-host disease (GVH
Externí odkaz:
https://doaj.org/article/9937a8aff2ce416b9faf055ca2881abd
Autor:
Helene M. Schoemans, Kathy Goris, Raf Van Durm, Steffen Fieuws, Sabina De Geest, Steven Z. Pavletic, Annie Im, Daniel Wolff, Stephanie J. Lee, Hildegard Greinix, Rafael F. Duarte, Xavier Poiré, Dominik Selleslag, Philippe Lewalle, Tessa Kerre, Carlos Graux, Frédéric Baron, Johan A. Maertens, Fabienne Dobbels
Publikováno v:
Haematologica, Vol 103, Iss 10 (2018)
Graft-versus-host disease (GvHD) assessment has been shown to be a challenge for healthcare professionals, leading to the development of the eGVHD App (www.uzleuven.be/egvhd). In this study, we formally evaluated the accuracy of using the App compare
Externí odkaz:
https://doaj.org/article/ef5082177aa242688cb0717a7838ddf2
Autor:
Mallory Taylor, Steve Cole, Joelle Strom, Ruta Brazauskas, Scott Baker, Rachel Phelan, David Buchbinder, Betty K. Hamilton, Prof. Helene M. Schoemans, Jennifer M. Knight
Publikováno v:
Blood. 140:911-913
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ef63b5bd83317931c10d61046e720ab
https://doi.org/10.1182/blood-2022-162545
https://doi.org/10.1182/blood-2022-162545
Autor:
Larisa Broglie, Stephanie Bo-Subait, Yue Chen, Ruta Brazauskas, David Buchbinder, Betty K. Hamilton, Helene M. Schoemans, Rachel Phelan, Prakash Satwani
Publikováno v:
Transplantation and Cellular Therapy. 28:S48-S49
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3235ed1b55be9ad165c669c7ee098c64
https://doi.org/10.1016/s2666-6367(22)00217-2
https://doi.org/10.1016/s2666-6367(22)00217-2
Autor:
Hanne Beeckmans, Gene P. L. Ambrocio, Saskia Bos, Astrid Vermaut, Vincent Geudens, Arno Vanstapel, Bart M. Vanaudenaerde, Frans De Baets, Thomas L. A. Malfait, Marie-Paule Emonds, Dirk E. Van Raemdonck, Hélène M. Schoemans, Robin Vos, for the Leuven Lung Transplant Group, Laurens J. Ceulemans, Geert M. Verleden, Lieven J. Dupont, Laurent Godinas, Veronique Schaevers, Dirk Claes, Karen Denaux, Bruno Desschans, Liesbeth Daniëls, Eric K. Verbeken, Birgit Weynand, Johny Verschakelen, Adriana Dubbeldam, Renata Haghedooren
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Pulmonary alveolar proteinosis (PAP) is a rare, diffuse lung disorder characterized by surfactant accumulation in the small airways due to defective clearance by alveolar macrophages, resulting in impaired gas exchange. Whole lung lavage is the curre
Externí odkaz:
https://doaj.org/article/bf55ee111e334d9b9b352399fc2653af