Article (Scientific journals)
La fibrose pulmonaire idiopathique.
GUIOT, Julien; CORHAY, Jean-Louis; Louis, Renaud
2014In Revue Médicale de Liège, 69 (11), p. 605-10
Peer reviewed
 

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Keywords :
Diagnostic Imaging/methods; Disease Progression; Humans; Idiopathic Pulmonary Fibrosis/diagnosis/etiology/therapy
Abstract :
[en] Idiopathic pulmonary fibrosis (IPF) is one of the multiple pathologies included in the large family of diffuse interstitial parenchymal lung diseases (IPD). The latter represent a large group of about 200 different diseases, most of which are orphan diseases. Recently, some new therapeutic options have appeared that require an early and accurate diagnosis of pulmonary fibrosis.
Disciplines :
Cardiovascular & respiratory systems
Author, co-author :
GUIOT, Julien  ;  Centre Hospitalier Universitaire de Liège - CHU > Pneumologie-Allergologie
CORHAY, Jean-Louis ;  Centre Hospitalier Universitaire de Liège - CHU > Pneumologie-Allergologie
Louis, Renaud ;  Université de Liège > Département des sciences cliniques > Pneumologie - Allergologie
Language :
French
Title :
La fibrose pulmonaire idiopathique.
Alternative titles :
[en] Idiopathic pulmonary fibrosis
Publication date :
November 2014
Journal title :
Revue Médicale de Liège
ISSN :
0370-629X
eISSN :
2566-1566
Publisher :
Université de Liège. Revue Médicale de Liège, Liège, Belgium
Volume :
69
Issue :
11
Pages :
605-10
Peer reviewed :
Peer reviewed
Available on ORBi :
since 09 July 2015

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