Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Pascal Zumstein"'
Autor:
Sabina A. Guler, Pascal Zumstein, Sabina Berezowska, Alexander Poellinger, Thomas Geiser, Manuela Funke-Chambour
Publikováno v:
Swiss Medical Weekly, Vol 148, Iss 0102 (2018)
BACKGROUND Idiopathic pulmonary fibrosis (IPF) differs substantially from other idiopathic interstitial pneumonias regarding disease trajectory and the appropriate management strategies, making meticulous diagnosis essential. However, patient charac
Externí odkaz:
https://doaj.org/article/b6b16cad89aa4f72a2685d3c028d6666
Autor:
Marc Kaethner, Matías Preza, Tobias Kaempfer, Pascal Zumstein, Claudia Tamponi, Antonio Varcasia, Andrew Hemphill, Klaus Brehm, Britta Lundström-Stadelmann
Echinococcus multilocularisandE. granulosus s.l.are the causative agents of alveolar and cystic echinococcosis, respectively. Drug treatment options for these severe and neglected diseases are limited to benzimidazoles, which are not always efficacio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07346519f327b060e225804ba24b09ea
https://doi.org/10.1101/2023.05.02.539024
https://doi.org/10.1101/2023.05.02.539024
Publikováno v:
Swiss Medical Forum ‒ Schweizerisches Medizin-Forum.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d88ae0a647e1764a5591590405dabb71
https://doi.org/10.4414/smf.2022.08888
https://doi.org/10.4414/smf.2022.08888
Autor:
Nenad Torbica, Lukas Ebner, Alexander Poellinger, Pascal Zumstein, Valentina Petroulia, Thomas Geiser, Sabina Berezowska, Manuela Funke, Johannes T. Heverhagen
Publikováno v:
Petroulia, Valentina Dafni; Funke-Chambour, Manuela; Zumstein, Pascal; Berezowska, Sabina Anna; Ebner, Lukas; Geiser, Thomas; Torbica, Nenad; Heverhagen, Johannes; Pöllinger, Alexander (2018). Increased Expiratory Computed Tomography Density Reveals Possible Abnormalities in Radiologically Preserved Lung Parenchyma in Idiopathic Pulmonary Fibrosis. Investigative radiology, 53(1), pp. 45-51. Lippincott Williams & Wilkins 10.1097/rli.0000000000000405
OBJECTIVES Idiopathic pulmonary fibrosis (IPF) is a progressive lethal chronic lung disease with unclear pathogenesis. Radiological hallmark is the pattern of usual interstitial pneumonia accentuated in peripheral and basal areas with otherwise prese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9d4f6e8ea7be3e6e8f60c46f78fadf9
https://doi.org/10.1097/rli.0000000000000405
https://doi.org/10.1097/rli.0000000000000405
Autor:
Sabina A. Guler, Alexander Pöllinger, Manuela Funke, Sabina Berezowska, Pascal Zumstein, Thomas Geiser
Publikováno v:
Chest. 151:A134
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3edc5bb302b9ec56c7a3952d9d285214
https://doi.org/10.1016/j.chest.2017.04.141
https://doi.org/10.1016/j.chest.2017.04.141
Autor:
Manuela Funke, Alexander Pöllinger, Pascal Zumstein, Lukas Ebner, V. Petroulia, Thomas Geiser
Publikováno v:
Chest. 151:A138
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b2392e934ae6c558d3d18e5a8fa4a05
https://doi.org/10.1016/j.chest.2017.04.145
https://doi.org/10.1016/j.chest.2017.04.145