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Comment j'explore ... une pneumopathie interstitielle diffuse
Bury, Thierry
1999In Revue Médicale de Liège, 54 (1), p. 54-7
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Abstract :
[en] There are a large number of conditions of known or unknown causes that have a tendency to alveolar wall fibrosis. The patient usually presents with progressive dyspnoea and the chest radiograph shows bilateral shadows whereas physiological measurements show a restrictive defect. Because of implications with regard to treatment and prognosis, diagnosis and staging of the disease are important. Computed tomography ("high resolution") and bronchoalveolar lavage are very useful at all stages of management of interstitial lung disease.
Disciplines :
Cardiovascular & respiratory systems
Author, co-author :
Bury, Thierry ;  Université de Liège - ULiège > Département des sciences de la motricité > Physiologie humaine et physiologie de l'effort physique
Language :
French
Title :
Comment j'explore ... une pneumopathie interstitielle diffuse
Alternative titles :
[en] How to Investigate ... Diffuse Interstitial Lung Disease
Publication date :
January 1999
Journal title :
Revue Médicale de Liège
ISSN :
0370-629X
eISSN :
2566-1566
Publisher :
Université de Liège. Revue Médicale de Liège, Liège, Belgium
Volume :
54
Issue :
1
Pages :
54-7
Peer reviewed :
Peer reviewed
Available on ORBi :
since 28 April 2014

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