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Num Mark Subjects (1-4 of 4) Year Entries
7 Found
1 Idiopathic Pulmonary Fibrosis   2
2 Idiopathic Pulmonary Fibrosis -- diagnosis.   2
3  

Idiopathic Pulmonary Fibrosis, Familial -- See Idiopathic Pulmonary Fibrosis


A common interstitial lung disease of unknown etiology, usually occurring between 50-70 years of age. Clinically, it is characterized by an insidious onset of breathlessness with exertion and a nonproductive cough, leading to progressive DYSPNEA. Pathological features show scant interstitial inflammation, patchy collagen fibrosis, prominent fibroblast proliferation foci, and microscopic honeycomb change
  1
4 Idiopathic Pulmonary Fibrosis -- therapy.   2
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