ライフサイエンスコーパス: interstitial pneumonia

1 usual interstitial pneumonia and nonspecific interstitial pneumonia.

2 CI 54-96) for underlying biopsy-proven usual interstitial pneumonia.

3 evelopment of several subtypes of idiopathic interstitial pneumonia.

4 squamative interstitial pneumonia, and acute interstitial pneumonia.

5 58 consecutive cases of suspected idiopathic interstitial pneumonia.

6 ether to establish a diagnosis of idiopathic interstitial pneumonia.

7 ost commonly encountered fibrotic idiopathic interstitial pneumonia.

8 l pneumonia and 29 patients with nonspecific interstitial pneumonia.

9 .08) compared with patients with nonspecific interstitial pneumonia.

10 usual interstitial pneumonia and nonspecific interstitial pneumonia.

11 seline features for patients with idiopathic interstitial pneumonia.

12 as associated with induced MIC expression in interstitial pneumonia.

13 of 238 patients with biopsy confirmed usual interstitial pneumonia.

14 indings that were more compatible with usual interstitial pneumonia.

15 so with hepatitis, conjunctivitis, and viral interstitial pneumonia.

16 ding SIV-induced encephalitis and lentivirus interstitial pneumonia.

17 ological and physiological manifestations of interstitial pneumonia.

18 of graft-versus-host disease (GVHD) and the interstitial pneumonia.

19 ad parotid gland enlargement and lymphocytic interstitial pneumonia.

20 RNA in lymphoid tissue, and viral associated interstitial pneumonia.

21 ngerhans cell histiocytosis, and lymphocytic interstitial pneumonia.

22 ommon pattern of presentation is nonspecific interstitial pneumonia.

23 me radiopathologic patterns as in idiopathic interstitial pneumonia.

24 as proven effective for chronic granulocytic interstitial pneumonia.

25 ry fibrosis (IPF) is a progressive and fatal interstitial pneumonia.

26 in SSc-ILD, whereas IPF is defined by usual interstitial pneumonia.

27 eumonia, and 18 as subtypes other than usual interstitial pneumonia.

28 ed by the histopathological pattern of usual interstitial pneumonia.

29 nfirmation of histological patterns of usual interstitial pneumonia.

30 itial pneumonia and management of idiopathic interstitial pneumonia.

31 ution CT images are not definitive for usual interstitial pneumonia.

32 set of respiratory distress caused by severe interstitial pneumonia.

33 monary fibrosis (IPF) is a fatal progressive interstitial pneumonia.

34 ial areas of fibrosis in patients with usual interstitial pneumonia.

35 features, including severe skin disease and interstitial pneumonia.

36 < 0.001) than for other subgroups of chronic interstitial pneumonias.

37 ed to treat acute exacerbation of idiopathic interstitial pneumonias.

38 sociated with sporadic and familial fibrotic interstitial pneumonias.

39 is, asks the question: is it all about usual interstitial pneumonia?

40 l interstitial pneumonia, 23 as non-specific interstitial pneumonia, 16 as hypersensitivity pneumonit

41 were identified by the expert panel as usual interstitial pneumonia, 23 as non-specific interstitial

42 characterized as either fibrotic nonspecific interstitial pneumonia (38%, 19 of 50) or variant fibros

43 requency of 34% among subjects with familial interstitial pneumonia, 38% among subjects with idiopath

44 in the lung among 83 subjects with familial interstitial pneumonia, 492 subjects with idiopathic pul

45 conditions (11.5%), or fibrosing nonspecific interstitial pneumonia (7.2%).

46 gh-resolution CT criteria for possible usual interstitial pneumonia (94.0%, 86.7-98.0).

47 interstitial pneumonia (UIP) or nonspecific interstitial pneumonia, a review of the histopathologic

48 ively established, it seems that nonspecific interstitial pneumonia accounts for a large proportion o

49 del infection is required for development of interstitial pneumonia after allogeneic BMT.

50 rolling the development of P. carinii-driven interstitial pneumonia after either syngeneic or allogen

51 ryptogenic organizing pneumonia (COP), acute interstitial pneumonia (AIP), and lymphoid interstitial

52 nterstitial pneumonia/fibrosis (NSIP), acute interstitial pneumonia (AIP), bronchiolitis, bronchiolit

53 families with 2 or more cases of idiopathic interstitial pneumonia among first-degree family members

54 ts in the paclitaxel plus gemcitabine group (interstitial pneumonia, anaphylaxis, and severe neutrope

55 nt protein C (L188Q SFTPC) found in familial interstitial pneumonia and (ii) intratracheal treatment

56 rospectively examined 80 patients with usual interstitial pneumonia and 29 patients with nonspecific

57 Desaturation was common (44 of 83 usual interstitial pneumonia and 8 of 22 nonspecific interstit

58 I, 3.8 to 113.7), respectively, for familial interstitial pneumonia and 9.0 (95% CI, 6.2 to 13.1) and

59 scan, we detected linkage between idiopathic interstitial pneumonia and a 3.4-Mb region of chromosome

60 As some patients with usual interstitial pneumonia and an underlying collagen vascul

61 fibrosis and a histologic diagnosis of usual interstitial pneumonia and evaluated the prognostic sign

62 ght control rhesus macaques exhibited severe interstitial pneumonia and high virus replication in the

63 the SLB group, mostly idiopathic nonspecific interstitial pneumonia and hypersensitivity pneumonitis,

64 romoter of MUC5B is associated with familial interstitial pneumonia and idiopathic pulmonary fibrosis

65 n mice with chronic hyperglycemia results in interstitial pneumonia and increased susceptibility to i

66 Affected pigs exhibited severe interstitial pneumonia and lymphoid depletion.

67 Pathologic assessment showed nonspecific interstitial pneumonia and major pulmonary vascular remo

68 gional sites familiar with patterns of usual interstitial pneumonia and management of idiopathic inte

69 s treated with pulse corticosteroid therapy, interstitial pneumonia and mediastinal emphysema deterio

70 minor gene expression changes between usual interstitial pneumonia and nonspecific interstitial pneu

71 Usual interstitial pneumonia and nonspecific interstitial pneu

72 ognostic information for patients with usual interstitial pneumonia and nonspecific interstitial pneu

73 The infected mice generated typical interstitial pneumonia and pathology that were similar t

74 ts into the early pathogenesis of idiopathic interstitial pneumonia and provide an ongoing opportunit

75 pared with fibroblast lines from nonspecific interstitial pneumonia and respiratory bronchiolitis/int

76 che, fatigue, and diarrhea and can end up in interstitial pneumonia and severe respiratory failure.

77 stitial lung diseases, including nonspecific interstitial pneumonia and usual interstitial pneumonia,

78 omplex lung diseases, notably the idiopathic interstitial pneumonias and small airways diseases, owes

79 hocytic interstitial pneumonia, desquamative interstitial pneumonia, and acute interstitial pneumonia

80 erstitial pneumonia, indeterminate for usual interstitial pneumonia, and alternative diagnosis; and f

81 th usual interstitial pneumonia, nonspecific interstitial pneumonia, and chronic hypersensitivity pne

82 om infected CCL3(-/-) mice suffered a milder interstitial pneumonia, and fewer immune cells were reco

83 usual interstitial pneumonia, possible usual interstitial pneumonia, and inconsistent with usual inte

84 the narrowed pathologic definition of usual interstitial pneumonia, and recognition of the prognosti

85 ibrosis, histopathological features of usual interstitial pneumonia, and reduced survival in patients

86 al interstitial pneumonia (UIP), nonspecific interstitial pneumonia, and respiratory bronchiolitis-in

87 iopsy had histologic findings of nonspecific interstitial pneumonia, and the seventh had bronchioliti

88 o diagnose, especially, in the case in which interstitial pneumonia appears in the course of gold the

89 ly to corticosteroid therapy, other forms of interstitial pneumonia are often steroid responsive and

90 Idiopathic interstitial pneumonias are a diverse group of lung dise

91 Idiopathic interstitial pneumonias are often complicated by pulmona

92 (aged 18-80 years) diagnosed with idiopathic interstitial pneumonia (as per American Thoracic Society

93 ogic analysis; one patient, with nonspecific interstitial pneumonia at CT but desquamative interstiti

94 gic analysis; and one patient, with lymphoid interstitial pneumonia at CT but nonspecific interstitia

95 ions were two patients classified with usual interstitial pneumonia at CT but with nonspecific inters

96 interstitial pneumonia at CT but nonspecific interstitial pneumonia at pathologic analysis.

97 nterstitial pneumonia at CT but desquamative interstitial pneumonia at pathologic analysis; and one p

98 stitial pneumonia at CT but with nonspecific interstitial pneumonia at pathologic analysis; one patie

99 flu-like symptoms are common with bilateral interstitial pneumonia being the most frightening presen

100 s: usual interstitial pneumonia, nonspecific interstitial pneumonia, bronchiolitis, and organizing pn

101 Both patients had associated nonspecific interstitial pneumonia but no signs of malignancy.

102 mice in response to P carinii does not cause interstitial pneumonia, but irradiation of the host befo

103 hat resolved to multifocal lymphohistiocytic interstitial pneumonia by 28 days.

104 Usual interstitial pneumonia by HRCT (P < 0.0002) and baseline

105 e Pulmonary Fibrosis, Thin-Section CT, Usual Interstitial Pneumonia (C) RSNA, 2024.

106 This interstitial pneumonia can be caused by the accumulation

107 This interstitial pneumonia can occur in infected mice after

108 interstitial pneumonia (IIP), such as usual interstitial pneumonia, can be impervious to modern ster

109 The interstitial pneumonia caused by allogeneic BMT and P ca

110 -however, it did not stop the development of interstitial pneumonia caused by the infiltration of hos

111 For patients with usual interstitial pneumonia, change in forced vital capacity

112 accinated or received empty vector developed interstitial pneumonia characterized by a marked alveoli

113 prolonged and exacerbated P. carinii-driven interstitial pneumonia characterized by eosinophilia and

114 terstitial pneumonia and 8 of 22 nonspecific interstitial pneumonia; chi square, p = 0.39).

115 The interstitial pneumonias comprise a diverse group of dise

116 Idiopathic interstitial pneumonias comprise usual interstitial pneu

117 36 patients with histologically proven usual interstitial pneumonia (CPI, p < 0.0005; FVC, p = 0.002;

118 more extensive in patients with nonspecific interstitial pneumonia CT pattern (P =.028).

119 Usual interstitial pneumonia and nonspecific interstitial pneumonia CT patterns overlapped; GGO was m

120 isks of graft-versus-host disease (GVHD) and interstitial pneumonia decreased over time, but the risk

121 pneumonia, organizing pneumonia, lymphocytic interstitial pneumonia, desquamative interstitial pneumo

122 ulmonary fibrosis or idiopathic non-specific interstitial pneumonia diagnosed within the preceding 6

123 rstitial lung disease (RB-ILD), desquamative interstitial pneumonia (DIP), Langerhans cell histiocyto

124 l interstitial pneumonia (UIP), desquamative interstitial pneumonia (DIP), nonspecific interstitial p

125 interstitial pneumonia (NSIP), desquamative interstitial pneumonia (DIP), respiratory bronchiolitis-

126 nia (UIP) (47%), NSIP (36%), or desquamative interstitial pneumonia (DIP)/respiratory bronchiolitis-a

127 ma-/- splenocytes which was characterized by interstitial pneumonia, eosinophilia, and multinucleated

128 with the severest form of IIP, namely usual interstitial pneumonia, exhibited the greatest gene and

129 63 after idiopathic pulmonary fibrosis/usual interstitial pneumonia fibroblast injection, patchy inte

130 Adoptively transferred nonspecific interstitial pneumonia fibroblasts caused a more diffuse

131 IL13-PE), the proliferation of primary usual interstitial pneumonia fibroblasts was inhibited to a mu

132 ve interstitial pneumonia (DIP), nonspecific interstitial pneumonia/fibrosis (NSIP), acute interstiti

133 Fibrotic idiopathic interstitial pneumonias (fIIP) are a group of fatal lung

134 tionale: Relatives of patients with familial interstitial pneumonia (FIP) are at increased risk for p

135 such as Birt-Hogg-Dube syndrome, lymphocytic interstitial pneumonia, follicular bronchiolitis, and li

136 itial pneumonia, and inconsistent with usual interstitial pneumonia) for confirmation of histological

137 he prognostic importance of separating usual interstitial pneumonia from other idiopathic interstitia

138 op a molecular test that distinguishes usual interstitial pneumonia from other interstitial lung dise

139 sitivity pneumonitis, and non-IPF idiopathic interstitial pneumonia from three U.S. centers and one U

140 Although usual interstitial pneumonia generally responds poorly to cort

141 ; 52 deaths occurred in the idiopathic usual interstitial pneumonia group (log rank; p = 0.005).

142 e collagen vascular disease-associated usual interstitial pneumonia group; 52 deaths occurred in the

143 Patients with idiopathic usual interstitial pneumonia had a higher median profusion of

144 ho met high-resolution CT criteria for usual interstitial pneumonia had histologically confirmed usua

145 Conclusion Participants with nonspecific interstitial pneumonia had increased barrier uptake and

146 h collagen vascular disease-associated usual interstitial pneumonia have fewer fibroblastic foci and

147 ncy virus-infected children with lymphocytic interstitial pneumonia have human immunodeficiency virus

148 n = 1) patterns typical for idiopathic usual interstitial pneumonia (idiopathic UIP) were entered int

149 Idiopathic interstitial pneumonia (IIP) and its familial variants a

150 4.9% of participants with non-IPF idiopathic interstitial pneumonia (IIP), 46.5% of participants with

151 lmonary fibrotic diseases such as idiopathic interstitial pneumonia (IIP), but it is not presently cl

152 Severe forms of idiopathic interstitial pneumonia (IIP), such as usual interstitial

153 ant in categorizing patients with idiopathic interstitial pneumonia (IIP).

154 th ILD-PH and relevant subgroups (idiopathic interstitial pneumonia [IIP], idiopathic pulmonary fibro

155 Idiopathic interstitial pneumonias (IIPs) are a collection of pulmo

156 The idiopathic interstitial pneumonias (IIPs) are a seemingly disconnec

157 ciety (ATS/ERS) classification of idiopathic interstitial pneumonias (IIPs) defined seven specific en

158 Idiopathic interstitial pneumonias (IIPs) have a progressive and of

159 , white individuals with fibrotic idiopathic interstitial pneumonias (IIPs; n = 1,616) and controls (

160 ndrome virus (PRRSV), which induces an acute interstitial pneumonia in pigs.

161 The classifier identified usual interstitial pneumonia in transbronchial lung biopsy sam

162 tations in the proSP-C sequence with chronic interstitial pneumonias in children and adults.

163 ients with other types of idiopathic chronic interstitial pneumonias including NSIP.

164 B for patterns of definite or probable usual interstitial pneumonia, indeterminate for usual intersti

165 ymphocytes and plasma cells in RA-associated interstitial pneumonia (IP) in comparison with idiopathi

166 spiratory tract infection (URTI; n=3) or RSV interstitial pneumonia (IP; n=12), all of whom also rece

167 he exploration of PF phenotypes beyond usual interstitial pneumonia/IPF.

168 Idiopathic pulmonary fibrosis (IPF)/usual interstitial pneumonia is a ravaging condition of progre

169 t of a genomic signature that predicts usual interstitial pneumonia is feasible.

170 The diagnosis of idiopathic interstitial pneumonia is made by means of correlation o

171 Nonspecific interstitial pneumonia is now better defined.

172 diopathic pulmonary fibrosis and nonspecific interstitial pneumonia is recognized to be heterogeneous

173 A histologic feature of usual interstitial pneumonia is the presence of fibroblastic f

174 milar to that associated with the idiopathic interstitial pneumonias is not known.

175 s (IPF), a chronic and progressive fibrosing interstitial pneumonia, is a fatal lung disease with a m

176 The histological pattern, known as usual interstitial pneumonia, is the archetype of progressive

177 Analyses of the microscopic-interstitial-pneumonia-lesion scores (0 to 6) revealed t

178 of children with AIDS-associated lymphocytic interstitial pneumonia (LIP) are unknown, we studied the

179 e interstitial pneumonia (AIP), and lymphoid interstitial pneumonia (LIP).

180 nonspecific interstitial pneumonia and usual interstitial pneumonia, making diagnosis extremely diffi

181 gh initially classified as a rare idiopathic interstitial pneumonia, many cases are related to known

182 stic infections, suggesting that lymphocytic interstitial pneumonia may reflect an effective antivira

183 [range, 38-93 years]), 244 with nonspecific interstitial pneumonia (men, 79; women, 165; median age,

184 t-degree relatives of patients with familial interstitial pneumonia.Methods: Enrollment evaluation in

185 with ACD (n = 12), adults with non-specific interstitial pneumonia (n = 12), and controls (n = 20) w

186 s with acute lung injury (n = 7) and chronic interstitial pneumonia (n = 14) were stained for detecti

187 interstitial pneumonia (n = 26), nonspecific interstitial pneumonia (n = 19), bronchiolitis (n = 11),

188 erstitial pneumonia (n = 83) and nonspecific interstitial pneumonia (n = 22).

189 our major CT patterns were identified: usual interstitial pneumonia (n = 26), nonspecific interstitia

190 ld predict mortality for patients with usual interstitial pneumonia (n = 83) and nonspecific intersti

191 logically confirmed as not or possible usual interstitial pneumonia (negative predictive value 18.3%,

192 l lung biopsies from 108 patients with usual interstitial pneumonia (nine with collagen vascular dise

193 and emphysema (CPFE) as well as nonspecific interstitial pneumonia (NIP), remains to be determined.

194 s is associated with four CT patterns: usual interstitial pneumonia, nonspecific interstitial pneumon

195 es: idiopathic pulmonary fibrosis with usual interstitial pneumonia, nonspecific interstitial pneumon

196 own from idiopathic pulmonary fibrosis/usual interstitial pneumonia, nonspecific interstitial pneumon

197 group of study participants with nonspecific interstitial pneumonia (NSIP) compared with healthy cont

198 Surgical lung biopsies disclosed nonspecific interstitial pneumonia (NSIP) in 18 of 22 patients (81.8

199 Patients with nonspecific interstitial pneumonia (NSIP) in all lobes were categori

200 al interstitial pneumonia (UIP), nonspecific interstitial pneumonia (NSIP), desquamative interstitial

201 interstitial pneumonia (UIP) and nonspecific interstitial pneumonia (NSIP), the most commonly encount

202 topathologic patterns, including nonspecific interstitial pneumonia (NSIP).

203 0.73 [0.68-0.78]); moderate for non-specific interstitial pneumonia (NSIP; kappaw=0.42 [0.37-0.49]);

204 demonstrating several subtypes of idiopathic interstitial pneumonia occurring within the same familie

205 m collagen vascular disease-associated usual interstitial pneumonia (odds ratio 8.31; 95% confidence

206 ious malignancies showed unexpected signs of interstitial pneumonia on CT and elevated regional (18)F

207 ients who had possible or inconsistent usual interstitial pneumonia on HRCT, the classifier showed 81

208 differentiated thyroid carcinoma also showed interstitial pneumonia on SPECT/CT.

209 In chronic interstitial pneumonia, only rare type II pneumocytes (<

210 monary infiltrates and suspected nonspecific interstitial pneumonia or idiopathic pulmonary fibrosis.

211 Patients with usual interstitial pneumonia or nonspecific interstitial pneum

212 Interstitial pneumonias or lymphoid organ lesions, simil

213 among first-degree family members (familial interstitial pneumonia, or FIP), and identified 111 fami

214 is/usual interstitial pneumonia, nonspecific interstitial pneumonia, or histologically normal biopsie

215 ng nonspecific interstitial pneumonia, usual interstitial pneumonia, organizing pneumonia, lymphocyti

216 .001), and 27 of 244 (11.1%) had nonspecific interstitial pneumonia (P < .001).

217 controls (allelic association with familial interstitial pneumonia, P=1.2x10(-15); allelic associati

218 d patients with ILD with a nondefinite usual interstitial pneumonia pattern (on high-resolution compu

219 nd an ILD that mimics a cellular nonspecific interstitial pneumonia pattern dominated by an interstit

220 A usual interstitial pneumonia pattern is a hallmark of idiopath

221 Histologically, a nonspecific interstitial pneumonia pattern is commonly observed in S

222 al setting, for patients with possible usual interstitial pneumonia pattern on high resolution CT, su

223 stitial lung disease without a typical usual interstitial pneumonia pattern on high-resolution comput

224 San Francisco, CA, USA) to identify a usual interstitial pneumonia pattern.

225 a definitive histological diagnosis of usual interstitial pneumonia pattern.

226 interstitial pneumonia from other idiopathic interstitial pneumonia patterns have profoundly changed

227 nary hypertension associated with idiopathic interstitial pneumonia (PH-IIP).

228 pneumonia had histologically confirmed usual interstitial pneumonia (positive predictive value 97.3%,

229 e of high-resolution CT (classified as usual interstitial pneumonia, possible usual interstitial pneu

230 verity into affected (all criteria for usual interstitial pneumonia present) and less affected (some

231 ffected (some but not all criteria for usual interstitial pneumonia present).

232 phocyte depletion of mesenteric lymph nodes, interstitial pneumonia, psoriatic skin lesions, and neur

233 with biopsies from patients with nonspecific interstitial pneumonia, respiratory bronchiolitis-inters

234 In contrast, non-specific interstitial pneumonia samples showed a regular basement

235 oracic Association guidelines (81.3%), usual interstitial pneumonia secondary to autoimmune condition

236 Neither CT involvement nor CT patterns of interstitial pneumonia showed differences across differe

237 A molecular usual interstitial pneumonia signature can be identified by a

238 st, tissue slices from human lung with usual interstitial pneumonia submitted to mechanical force sho

239 ore accurate prognostic determinant in usual interstitial pneumonia than an individual pulmonary func

240 ation developed a more protracted and severe interstitial pneumonia than that of normal mice given P

241 sistent high-resolution CT pattern for usual interstitial pneumonia that was histologically confirmed

242 In patients with usual interstitial pneumonia, the presence of desaturation was

243 rus-infected individuals develop lymphocytic interstitial pneumonia, the roles of host and viral fact

244 organising pneumonia as in other idiopathic interstitial pneumonias, the characteristic pattern of t

245 y fibrosis (IPF) requires a pattern of usual interstitial pneumonia to be present on high-resolution

246 d-resistant acute exacerbation of idiopathic interstitial pneumonias treated with blood purification

247 g idiopathic pulmonary fibrosis of the usual interstitial pneumonia type (IPF/UIP) were reviewed.

248 In chronic interstitial pneumonia, type II pneumocytes proliferate

249 by two pulmonary histopathologists as usual interstitial pneumonia (UIP) (47%), NSIP (36%), or desqu

250 osis of the histopathologic pattern of usual interstitial pneumonia (UIP) and clinical IPF.

251 were quantified, and guideline-defined usual interstitial pneumonia (UIP) and fibrotic hypersensitivi

252 ngiogenesis markers between histologic usual interstitial pneumonia (UIP) and non-UIP were assessed u

253 he histopathologic distinction between usual interstitial pneumonia (UIP) and nonspecific interstitia

254 particularly when typical features of usual interstitial pneumonia (UIP) are identified.

255 prospectively studied 87 patients with usual interstitial pneumonia (UIP) confirmed by surgical lung

256 -resolution chest scan (HRCT), and the usual interstitial pneumonia (UIP) histologic pattern.

257 organizing pneumonia (BOOP) in 1, and usual interstitial pneumonia (UIP) in 1.

258 Patients with usual interstitial pneumonia (UIP) in all lobes were categoriz

259 pecific features of TBLC predictive of usual interstitial pneumonia (UIP) in corresponding SLB and to

260 The usual interstitial pneumonia (UIP) incidence was higher in the

261 erstitial lung diseases that share the usual interstitial pneumonia (UIP) injury pattern.

262 Rationale: Usual interstitial pneumonia (UIP) is the defining morphology

263 y of patterns suggestive of underlying usual interstitial pneumonia (UIP) or nonspecific interstitial

264 surgical lung biopsy and to compare a usual interstitial pneumonia (UIP) pattern at CT with survival

265 scored for the extent of fibrosis and usual interstitial pneumonia (UIP) pattern.

266 diagnostic guidelines for IPF based on usual interstitial pneumonia (UIP) patterns, the pooled kappa

267 showed a heterogeneous group including usual interstitial pneumonia (UIP), desquamative interstitial

268 athic interstitial pneumonias comprise usual interstitial pneumonia (UIP), nonspecific interstitial p

269 ry fibroblast lines from patients with usual interstitial pneumonia (UIP), nonspecific interstitial p

270 culation, without atypical features of usual interstitial pneumonia (UIP), on high-resolution compute

271 Usual interstitial pneumonia (UIP), the pathologic correlate o

272 and validated in the identification of usual interstitial pneumonia (UIP)-like features on HRCT (UIP

273 tures that overlap with IPF, including usual interstitial pneumonia (UIP)-pattern disease characteriz

274 evaluation of patients with suspected usual interstitial pneumonia (UIP).

275 ified a population of fibroblasts from usual interstitial pneumonia (UIP)/idiopathic pulmonary fibros

276 in rheumatic diseases, including nonspecific interstitial pneumonia, usual interstitial pneumonia, or

277 conditions, including nonspecific pneumonia, interstitial pneumonia, viral pneumonia, consolidation,

278 diologic features, and metabolic activity of interstitial pneumonia were identified, correlated with

279 Patients with usual interstitial pneumonia were more likely to have a statis

280 usual interstitial pneumonia or nonspecific interstitial pneumonia who desaturated had a significant

281 LD lung LNs excised at transplant (30 IPF, 7 interstitial pneumonia with autoimmune features, 4 hyper

282 olate mofetil use and presence or absence of interstitial pneumonia with autoimmune features.

283 s characterized by a moderate self-resolving interstitial pneumonia with bronchiolitis of 21 days in

284 at first presented itself radiologically as interstitial pneumonia with pleural effusion and clinica

285 eloped severe cyanosis, tachypnea, and acute interstitial pneumonia, with RESTV shedding from oronasa

286 Marmosets had minimal to mild multifocal interstitial pneumonia, with the greatest relative sever

287 MERS-CoV caused a multifocal, mild to marked interstitial pneumonia, with virus replication occurring