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1 der with histologic features consistent with interstitial pneumonitis.
2 cal pattern of lung injury to a neutrophilic interstitial pneumonitis.
3 included fever, malaise, cough, dyspnea, and interstitial pneumonitis.
4 nitis and children with cellular nonspecific interstitial pneumonitis.
5 d with familial desquamative and nonspecific interstitial pneumonitis.
6 on of alveolar type II cells that results in interstitial pneumonitis.
7 e necrotizing bronchitis, bronchiolitis, and interstitial pneumonitis.
8 a mononuclear cell pulmonary vasculitis and interstitial pneumonitis.
9 cluding moderate to severe diffuse edema and interstitial pneumonitis.
10 mals developed a multifocal mononuclear cell interstitial pneumonitis, accompanied by multinucleated
11 onary pathology consisting of alveolitis and interstitial pneumonitis after a live-virus challenge.
12 ibrosis kindred, including adults with usual interstitial pneumonitis and children with cellular nons
13 associated pathological findings, including interstitial pneumonitis and consolidation, is also rema
14 ts with stable IPF compared with nonspecific interstitial pneumonitis and controls, which rose sharpl
15 ells resulted in an enhanced immune-mediated interstitial pneumonitis and delayed clearance of SARS-C
16 squamous cell lung cancer encountered severe interstitial pneumonitis and nodular regenerative hyperp
18 n with a referring diagnosis of desquamative interstitial pneumonitis and who were older than 10 year
19 mutant mice also have allergic blepharitis, interstitial pneumonitis, and a 10(3) to 10(4) fold incr
21 coscopic lung biopsy shows findings of usual interstitial pneumonitis, and he has no identifiable cau
22 f the red pulp of the spleen by macrophages, interstitial pneumonitis, and increased numbers of immat
23 evidence supporting the existence of chronic interstitial pneumonitis associated with nylon flock pro
24 ncluding lymphocytic alveolitis, lymphocytic interstitial pneumonitis, bronchoalveolar obliterans org
25 itantly, the animals developed a progressive interstitial pneumonitis characterized initially by lymp
26 d multinucleated giant cells and exacerbated interstitial pneumonitis compared with mice treated with
28 nduce several adverse effects, such as fibro-interstitial pneumonitis due to the acquisition of activ
29 ages 16, 23, and 11 years) with desquamative interstitial pneumonitis had ABCA3 mutations identified
32 a mouse model of MC deficiency, MC-dependent interstitial pneumonitis, hemorrhaging, and edema in the
33 gamma in the development of infection-driven interstitial pneumonitis in a model of murine graft-vers
34 erevisiae can induce arthritis, ileitis, and interstitial pneumonitis in BALB/c ZAP70 (W163C)-mutant
35 em cell transplantation patients who develop interstitial pneumonitis include idiopathic pneumonia sy
37 y specimens from patients with RA-associated interstitial pneumonitis (IP) were examined by immunohis
38 7 patients without Pneumocystis, nonspecific interstitial pneumonitis (NSIP) was the most common hist
39 s obliterans organizing pneumonia (BOOP) and interstitial pneumonitis occurred at 4 to 6 weeks, and 6
40 elated adverse events, including one grade 3 interstitial pneumonitis, one grade 4 polymyositis, and
43 inated Mycobacterium avium complex, lymphoid interstitial pneumonitis, systemic fungal infection, cyt
44 s into transgenic animals resulted extensive interstitial pneumonitis that was antigen-specific and a
47 of ACR, lymphocytic bronchiolitis, BOOP, and interstitial pneumonitis were directly associated with t
49 differences in severities in alveolitis and interstitial pneumonitis when each of the three variants
50 FG vaccine showed quite mild alveolitis and interstitial pneumonitis, which were eliminated by the a