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Idiopathic Pulmonary Fibrosis

descriptionPublicationkeyboard_double_arrow_right Article 10 May 2018 Italy English Publisher:Massachusetts Medical SocietyJournal:New England Journal of Medicine, volume 378, pages 1,811-1,823 (issn: 0028-4793, eissn: 1533-4406,

Authors: Poletti Venerino; Tomassetti S; Ravaglia Claudia;

doi: 10.1056/nejmra1705751 , 10.1056/nejmc1807508

pmid: 30136548 , 30136547 , 30134133 , 30136549 , 30136550 , 29742380

handle: 11585/1008340 , 2158/1241058

Idiopathic Pulmonary Fibrosis

- Summary
- Subjects
- Metrics

Abstract

Idiopathic Pulmonary Fibrosis Idiopathic pulmonary fibrosis appears to be increasing in incidence. It requires early recognition and intervention with supportive care and pharmacologic agents to forestall its progression. Lung transplantation may be curative, but the disease may recur in transplanted lungs.

Country

Italy

Related Organizations

Alma Mater Studiorum University of Bologna
Italy
Cornell University
United States
University of Florence
Italy
Korea University
Korea (Republic of)
Aarhus University Hospital
Denmark

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Keywords

Indoles, Pyridones, Oxygen Inhalation Therapy, Prognosis, Idiopathic Pulmonary Fibrosis, Diagnosis, Differential, Dyspnea, Idiopathic Pulmonary Fibrosis, IPF, Risk Factors, Transforming Growth Factor beta, Humans, Enzyme Inhibitors, Tomography, X-Ray Computed, Lung

Impact byBIP!

	citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	1K
	popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.	Top 0.01%
	influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	Top 0.1%
	impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.	Top 0.01%