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1 es to the development of several subtypes of idiopathic interstitial pneumonia.
2 s reviewed 58 consecutive cases of suspected idiopathic interstitial pneumonia.
3 st work together to establish a diagnosis of idiopathic interstitial pneumonia.
4 SIP), the most commonly encountered fibrotic idiopathic interstitial pneumonia.
5 ation to baseline features for patients with idiopathic interstitial pneumonia.
6 with the same radiopathologic patterns as in idiopathic interstitial pneumonia.
7 ual interstitial pneumonia and management of idiopathic interstitial pneumonia.
8 A may be used to treat acute exacerbation of idiopathic interstitial pneumonias.
9 e evaluated families with 2 or more cases of idiopathic interstitial pneumonia among first-degree fam
10 de linkage scan, we detected linkage between idiopathic interstitial pneumonia and a 3.4-Mb region of
11  new insights into the early pathogenesis of idiopathic interstitial pneumonia and provide an ongoing
12 anding of complex lung diseases, notably the idiopathic interstitial pneumonias and small airways dis
13                                              Idiopathic interstitial pneumonias are a diverse group o
14                                              Idiopathic interstitial pneumonias are often complicated
15 ere adults (aged 18-80 years) diagnosed with idiopathic interstitial pneumonia (as per American Thora
16                                              Idiopathic interstitial pneumonias comprise usual inters
17                                     Fibrotic idiopathic interstitial pneumonias (fIIP) are a group of
18 ic hypersensitivity pneumonitis, and non-IPF idiopathic interstitial pneumonia from three U.S. center
19                                              Idiopathic interstitial pneumonia (IIP) and its familial
20 CTD-ILD), 44.9% of participants with non-IPF idiopathic interstitial pneumonia (IIP), 46.5% of partic
21  chronic pulmonary fibrotic diseases such as idiopathic interstitial pneumonia (IIP), but it is not p
22                              Severe forms of idiopathic interstitial pneumonia (IIP), such as usual i
23  are important in categorizing patients with idiopathic interstitial pneumonia (IIP).
24 Patients with ILD-PH and relevant subgroups (idiopathic interstitial pneumonia [IIP], idiopathic pulm
25                                              Idiopathic interstitial pneumonias (IIPs) are a collecti
26                                          The idiopathic interstitial pneumonias (IIPs) are a seemingl
27 piratory Society (ATS/ERS) classification of idiopathic interstitial pneumonias (IIPs) defined seven
28                                              Idiopathic interstitial pneumonias (IIPs) have a progres
29 on-Hispanic, white individuals with fibrotic idiopathic interstitial pneumonias (IIPs; n = 1,616) and
30                             The diagnosis of idiopathic interstitial pneumonia is made by means of co
31 sease is similar to that associated with the idiopathic interstitial pneumonias is not known.
32      Although initially classified as a rare idiopathic interstitial pneumonia, many cases are relate
33  pedigrees demonstrating several subtypes of idiopathic interstitial pneumonia occurring within the s
34 ting usual interstitial pneumonia from other idiopathic interstitial pneumonia patterns have profound
35 s for pulmonary hypertension associated with idiopathic interstitial pneumonia (PH-IIP).
36  pattern of organising pneumonia as in other idiopathic interstitial pneumonias, the characteristic p
37 with steroid-resistant acute exacerbation of idiopathic interstitial pneumonias treated with blood pu