Literature DB >> 4112056

The concept of classic interstitial pneumonitis-fibrosis (CIP-F) as a clinicopathologic syndrome.

R A DeRemee, E G Harrison, H A Andersen.   

Abstract

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Year:  1972        PMID： 4112056     DOI： 10.1378/chest.61.3.213

Source DB:  PubMed          Journal:  Chest        ISSN： 0012-3692            Impact factor:   9.410


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  5 in total

1.  Small airways in idiopathic pulmonary fibrosis. Comparison of morphologic and physiologic observations.

Authors:  R G Crystal; J D Fulmer; W C Roberts; E R von Gal
Journal:  J Clin Invest       Date:  1977-09       Impact factor: 14.808

Review 2.  Pathophysiology of diffuse interstitial lung disease.

Authors:  J M Stinson
Journal:  J Natl Med Assoc       Date:  1974-07       Impact factor: 1.798

3.  Immunofluorescent staining of lung biopsy in fibrosing alveolitis.

Authors:  M C Poon; S W Epstein; H Sepp
Journal:  Can Med Assoc J       Date:  1973-03-17       Impact factor: 8.262

4.  Idiopathic pulmonary fibrosis in infants: good prognosis with conservative management.

Authors:  D Hacking; R Smyth; N Shaw; G Kokia; H Carty; D Heaf
Journal:  Arch Dis Child       Date:  2000-08       Impact factor: 3.791

5.  Progressive dyspnea in a 39-year-old housewife.

Authors:  U P Steinbrecher; N S Wang
Journal:  Can Med Assoc J       Date:  1980-03-22       Impact factor: 8.262
  5 in total

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