Screening for idiopathic pulmonary fibrosis using comorbidity signatures in electronic health records
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine
Link
https://www.nature.com/articles/s41591-022-02010-y.pdf
Reference82 articles.
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2. Raghu, G., Remy-Jardin, M. & Myers, J. Diagnosis of idiopathic pulmonary fibrosis. an official ats/ers/jrs/alat clinical practice guideline. Am. J. Respir. Crit. Care Med. 198, 44–68 (2018).
3. Raghu, G. Idiopathic pulmonary fibrosis: shifting the concept to irreversible pulmonary fibrosis of many entities. Lancet Respir. Med. 7, 926–929 (2019).
4. Ley, B., Collard, H. & King, T., Jr. Clinical course and prediction of survival in idiopathic pulmonary fibrosis. Am. J. Respir. Crit. Care Med. 183, 431–440 (2011).
5. Antoniou, K., Symvoulakis, E., Margaritopoulos, G., Lionis, C. & Wells, A. Early diagnosis of IPF: time for a primary-care case-finding initiative? Lancet Respir. Med. 2, 1 (2014).
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