Nonspecific interstitial pneumonia and usual interstitial pneumonia with mutation in surfactant protein C in familial pulmonary fibrosis

Author:

Chibbar Rajni,Shih Francis,Baga Monica,Torlakovic Emina,Ramlall Kumar,Skomro Robert,Cockcroft Donald W,Lemire Edmond G

Publisher

Springer Science and Business Media LLC

Subject

Pathology and Forensic Medicine

Reference32 articles.

1. American Thoracic Society, European Respiratory Society International. American Thoracic Society/European Respiratory Society International: multidisciplinary consensus classification of the idiopathic interstitial pneumonias. Am J Respir Crit Care Med 2002;165:277–304.

2. Adelman AG, Chertkow G, Hayton RC . Familial fibrocystic pulmonary dysplasia: a detailed family study. Can Med Assoc J 1966;95:603–610.

3. Bitterman PB, Rennard SI, Keogh BA, et al. Familial idiopathic pulmonary fibrosis: evidence of lung inflammation in unaffected family members. N Engl J Med 1986;314:1343–1347.

4. Donohue WL, Laski B, Uchida I, et al. Familial fibrocystic pulmonary dysplasia and its relation to the hamman-rich syndrome. Pediatrics 1959;24:786–813.

5. Hewitt CJ, Hull D, Keeling JW . Fibrosing alveolitis in infancy and childhood. Arch Dis Child 1977;52:22–37.

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