Prognostic significance of histopathologic subsets in idiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis (IPF) is a generally fatal disorder with a reported median survival of 3 to 6 yr. This has been based on relatively few studies with diagnoses inconsistently confirmed by adequate lung biopsy. Retrospective analysis of 104 patients with IPF who had open lung biopsy (OLB...
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Veröffentlicht in: | American journal of respiratory and critical care medicine 1998, Vol.157 (1), p.199-203 |
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