CareLit · DOI-Nachweis · Pneumologie
Role of Phosphodiesterases in Idiopathic Pulmonary Fibrosis
DOI 10.1055/s-2006-933826
Bibliografische Angaben
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Autor:innenS Nikolova, S Pullamsetti, A Ghofrani, N Weissmann, W Seeger, F Grimminger, R Schermuly
ZeitschriftPneumologie
Ausgabe04/2006
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Idiopathic pulmonary fibrosis (IPF) is a chronic progressive interstitial lung disease with a fatal outcome. The underlying causes of IPF are currently unknown and there is no available drug therapy that effectively blocks or reverses the progressive scarring of the lung. Drugs which interfere with the cyclic nucleotide levels have profound effects on regulation of airway smooth muscle tone, activation of inflammato…
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Zitierempfehlung
S Nikolova, S Pullamsetti, A Ghofrani, N Weissmann, W Seeger, F Grimminger, R Schermuly (2006) Role of Phosphodiesterases in Idiopathic Pulmonary Fibrosis. Pneumologie (04). https://doi.org/10.1055/s-2006-933826
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