Surfactant Protein C Deficiency-associated Diffuse Lung Disease
Author:
Affiliation:
1. Le Bonheur Children’s Hospital, The University of Tennessee Health Science Center
Publisher
Anderson Publishing, Ltd.
Reference10 articles.
1. Zucker EJ, Guillerman RP, Fishman MP, Casey AM, Lillehei CW and Lee EY. Diffuse Lung disease. In: Coley BD, Bates DG, editors. Caffey’s Pediatric Diagnostic Imaging. Elsevier Saunders: Philadelphia; 2013. pp. 595-597.
2. An official American Thoracic Society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancy;Kurland;Am J Respir Crit Care Med,2013
3. Childhood interstitial lung disease due to surfactant protein C deficiency: frequent use and costs of hospital services for a single case in Australia;Hime;Orphanet J Rare Dis,2014
4. Current update on iInterstitial lung disease of infancy: new classification system, diagnostic evaluation, imaging algorithms, imaging findings, and prognosis;Thacker;Radiol Clin North Am,2016
5. Clinical and genetic spectrum of interstitial lung disease in Chinese children associated with surfactant protein C mutations;Hong;Ital J Pediatr,2019
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