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The Diagnosis and Treatment of Idiopathic Pulmonary Fibrosis

BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is the most common idiopathic interstitial disease of the lung and has the worst prognosis of all such diseases, with a median survival time of three to four years. Its prevalence is 2–29 per 100 000 persons and its incidence approximately 10 per 100 0...

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Autor principal: Behr, Jürgen
Format: Artigo
Idioma:Inglês
Publicat: Deutscher Arzte Verlag 2013
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3928534/
https://ncbi.nlm.nih.gov/pubmed/24529303
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3238/arztebl.2013.0875
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