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Evidence of defective surfactant biosynthesis in patients with Idiopathic Pulmonary Fibrosis (IPF)

M Korfei, P Mahavadi, P Markart, C Ruppert, W Seeger, A Günther · Pneumologie · Ausgabe 01/2006

DOI 10.1055/s-2005-925494

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Autor:innenM Korfei, P Mahavadi, P Markart, C Ruppert, W Seeger, A Günther
ZeitschriftPneumologie
Ausgabe01/2006
Jahrgang / SeitenNicht angegeben

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Abstract-Vorschau

Rationale: Idiopathic pulmonary fibrosis (IPF) is one of the most common forms of interstitial lung disease, however, the aetiology of IPF is poorly understood. An increasingly favoured working hypothesis suggests that epithelial injury is the primary triggering event. In this regard, abnormalities in expression and processing of the hydrophobic surfactant proteins SP-B and SP-C are suggested to contribute to the pa…

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Zitierempfehlung

M Korfei, P Mahavadi, P Markart, C Ruppert, W Seeger, A Günther (2006) Evidence of defective surfactant biosynthesis in patients with Idiopathic Pulmonary Fibrosis (IPF). Pneumologie (01). https://doi.org/10.1055/s-2005-925494

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