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Idiopathic Pulmonary Fibrosis: Best Practice in Monitoring and Managing a Relentless Fibrotic Disease

Wuyts, W. A. (author)
Wijsenbeek, M. (author)
Bondue, B. (author)
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Bouros, D. (author)
Bresser, P. (author)
Cordeiro, C. R. (author)
Hilberg, O. (author)
Magnusson, Jesper (author)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för invärtesmedicin och klinisk nutrition,Institute of Medicine, Department of Internal Medicine and Clinical Nutrition
Manali, E. D. (author)
Morais, A. (author)
Papiris, S. (author)
Shaker, S. (author)
Veltkamp, M. (author)
Bendstrup, E. (author)
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 (creator_code:org_t)
2019-12-12
2020
English.
In: Respiration. - : S. Karger AG. - 0025-7931 .- 1423-0356. ; 99:1, s. 73-82
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Idiopathic pulmonary fibrosis (IPF) is a fibrosing interstitial lung disease that is, by definition

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine (hsv//eng)

Keyword

Nintedanib
Pirfenidone
Interstitial lung disease
Therapeutics
Treatment
Mortality
forced vital capacity
quality-of-life
clinical-practice
acute
exacerbation
lung-transplant
antacid therapy
home spirometry
palliative care
position paper
survival
Respiratory System

Publication and Content Type

ref (subject category)
art (subject category)

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