CareLit · DOI-Nachweis · Pneumologie
Integrative molecular and anatomical characterization of idiopathic pulmonary fibrosis
DOI 10.1055/s-0034-1376804
Bibliografische Angaben
Nachweis in CareLit
Autor:innenJ Wehling, M Kellner, N Izykowski, P Braubach, G Warnecke, L Knudsen, A Haverich, B Wiegmann, J Vogel-Claussen, H Kreipe, F Länger, M Kühnel, D Jonigk
ZeitschriftPneumologie
Ausgabe06/2014
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Rationale: Idiopathic pulmonary fibrosis (IPF) is a chronic, debilitating disease which is characterized by excessive collagen deposition and destruction of lung architecture leading to respiratory insufficiency. Lung transplantation still remains the only definite therapeutic option, since the etiology of IPF is poorly understood and no adequate medical treatment is currently available. In IPF there appears to be a…
Zitieren
Zitierempfehlung
J Wehling, M Kellner, N Izykowski, P Braubach, G Warnecke, L Knudsen, A Haverich, B Wiegmann, J Vogel-Claussen, H Kreipe, F Länger, M Kühnel, D Jonigk (2014) Integrative molecular and anatomical characterization of idiopathic pulmonary fibrosis. Pneumologie (06). https://doi.org/10.1055/s-0034-1376804
Mit CareLit weiterarbeiten