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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 ual interstitial pneumonia and management of idiopathic interstitial pneumonia.
7 A may be used to treat acute exacerbation of idiopathic interstitial pneumonias.
8 e evaluated families with 2 or more cases of idiopathic interstitial pneumonia among first-degree fam
9 de linkage scan, we detected linkage between idiopathic interstitial pneumonia and a 3.4-Mb region of
10 new insights into the early pathogenesis of idiopathic interstitial pneumonia and provide an ongoing
11 anding of complex lung diseases, notably the idiopathic interstitial pneumonias and small airways dis
16 chronic pulmonary fibrotic diseases such as idiopathic interstitial pneumonia (IIP), but it is not p
21 piratory Society (ATS/ERS) classification of idiopathic interstitial pneumonias (IIPs) defined seven
23 on-Hispanic, white individuals with fibrotic idiopathic interstitial pneumonias (IIPs; n = 1,616) and
26 pedigrees demonstrating several subtypes of idiopathic interstitial pneumonia occurring within the s
27 ting usual interstitial pneumonia from other idiopathic interstitial pneumonia patterns have profound
28 with steroid-resistant acute exacerbation of idiopathic interstitial pneumonias treated with blood pu
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