コーパス検索結果 (left1)
通し番号をクリックするとPubMedの該当ページを表示します
1 ILD events were more common among those with early/mild
2 ILD pattern was defined by high-resolution computed tomo
3 ILD was independently associated with IHD and HF, both o
6 cHL and heart disease (EAR, 6.6; SMR, 1.7), ILD (EAR, 3.7; SMR, 13.1), and infections (EAR, 3.1; SMR
7 patients with alternative idiopathic ILDs (a-ILD; n = 41), and healthy control subjects (n = 127).
10 body mass, craniomandibular CS, and absolute ILDs including skull, basicranial, palatal, mandibular,
12 develops both inflammatory arthritis and an ILD that mimics a cellular nonspecific interstitial pneu
14 ith sufficient study time, 25 (19.4%) had an ILD event by 5 years after enrollment; of these, 12 met
16 of interstitial lung abnormalities (ILA) and ILD among relatives of patients with FPF and sporadic IP
17 uroendocrine cell hyperplasia of infancy and ILD, due to mutations in genes affecting surfactant prod
20 , which reduced the dynamic range of ITD and ILD response functions and the ability of neurons to sig
21 Using a modeling approach, we assess ITD and ILD sensitivity of the neural filters to natural sounds,
22 conditions, cortical sensitivity to ITD and ILD takes the form of broad contralaterally dominated re
25 perates in a similar manner on both ITD- and ILD-sensitive neurons, suggesting a shared mechanism ope
29 As altered the relationship between ITDs and ILDs, introducing large ITD-ILD conflicts in some cases.
30 atients with rheumatoid arthritis-associated ILD (RA-ILD; n = 33), patients with alternative idiopath
32 e pathogenesis of fibrosis in SSc-associated ILD (SSc-ILD) involves cellular injury, activation/diffe
33 ncoding of ILDs, human and animal behavioral ILD sensitivity is robust to temporal stimulus degradati
37 In contrast, one BRICHOS and one non-BRICHOS ILD-associated mutant could not insert into membranes.
40 l lung disease (ILD) cases, (2) characterize ILD subgroups in an unbiased fashion, and (3) identify c
41 fants, who are regarded as having "childhood ILD syndrome"; (4) describe a new pathologic classificat
42 les that are highly effective in classifying ILD patients; and (3) stochastic simulation to design, t
43 inhibitory from the other: EI cells) compare ILDs separately over restricted frequency ranges which a
45 nor age on survival in recipients with COPD, ILD, or in the "other" group in multivariate models.
46 t localization cues are integrated: cortical ILD tuning to broadband sounds is a composite of separat
47 mmon new-onset ILD in India, followed by CTD-ILD and idiopathic pulmonary fibrosis; diagnoses varied
48 (n = 513; exposure, 48.1% air coolers), CTD-ILD in 13.9%, and idiopathic pulmonary fibrosis in 13.7%
53 l plane uses an interaural-level difference (ILD) cue, yet little is known about the synaptic mechani
54 is modulated by interaural level difference (ILD) primarily through scaling excitation to different l
55 rences (ITDs), interaural level differences (ILDs) and the direction-dependent spectral filtering by
57 igs to compare interaural level differences (ILDs), a key localization cue, between tones of disparat
58 rences (ITDs), interaural level differences (ILDs), and pinna spectral cues, are all represented in t
59 tween a side-emitting injection laser diode (ILD) and a dielectric optical waveguide mixer via a grad
60 try (FC) data and interstitial lung disease (ILD) - a systemic sclerosis (SSc, or scleroderma) clinic
61 n toward clinical interstitial lung disease (ILD) among subjects in a longitudinal cohort of self-rep
62 rlying dyspnea in interstitial lung disease (ILD) and chronic obstructive pulmonary disease (COPD) ar
63 ts with fibrosing interstitial lung disease (ILD) and determine whether there are differences among t
64 in patients with interstitial lung disease (ILD) and may reflect immunologic activation and subseque
65 gold standard-in interstitial lung disease (ILD) cases requiring histology remains controversial.
66 across end-stage interstitial lung disease (ILD) cases, (2) characterize ILD subgroups in an unbiase
67 rogressive, fatal interstitial lung disease (ILD) characterized by abnormal extracellular matrix (ECM
68 ts suffering from interstitial lung disease (ILD) due to mutations in the gene of the precursor prote
69 on patients with interstitial lung disease (ILD) has not been established.Objectives: To assess outc
71 recognition that interstitial lung disease (ILD) in infants is often distinct from the forms that oc
77 is a progressive interstitial lung disease (ILD) of unknown origin characterized by epithelial cell
78 of more advanced Interstitial Lung Disease (ILD) patterns, few have tackled ILA, which likely preced
81 y disease (COPD), interstitial lung disease (ILD), and "other." Intensive care unit (ICU) length of s
82 COPD), asthma and interstitial lung disease (ILD), and individual cardiovascular diseases, and evalua
83 ncreased risk for interstitial lung disease (ILD), the risk among relatives of sporadic idiopathic pu
84 or unclassifiable interstitial lung disease (ILD), which is characterised by progressive fibrosis of
91 isease (COPD) and interstitial lung disease (ILD).Methods: The multidisciplinary panel created six re
92 10.6; SMR, 3.9), interstitial lung disease (ILD; EAR, 9.7; SMR, 22.1), and adverse events (AEs) rela
96 ressive fibrotic interstitial lung diseases (ILDs) are characterised by major reductions in quality o
98 nal follow-up of interstitial lung diseases (ILDs) at CT mainly relies on the evaluation of the exten
99 ch as asthma and interstitial lung diseases (ILDs), including idiopathic pulmonary fibrosis (IPF) and
104 olliculus (of chinchilla) effectively encode ILDs despite complete decorrelation of left- and right-e
106 CC; Jaipur, India) with MDD, and experienced ILD experts at the Center for ILD (CILD; Seattle, WA) wi
108 ion DPO is common in patients with fibrosing ILD and is significantly more prevalent in patients with
109 ised 892 consecutive patients with fibrosing ILD, including 456 patients with idiopathic pulmonary fi
110 with IPF than in those with other fibrosing ILDs, and thus, computed tomographic signs of DPO may be
111 rosis from non-idiopathic pulmonary fibrosis ILD and used lung function to determine the greatest ris
112 ective implementation of palliative care for ILD will require multidisciplinary participation from cl
115 with ILA, 19 (58%) had further evidence for ILD (defined by the combination of imaging findings and
121 e in fibroblasts and in tissue sections from ILD patients and in lungs of bleomycin-treated mice.
122 , 50% of the subjects with SSc (n = 324) had ILD by HRCT and 46% displayed pulmonary function decline
123 ted in a subset of subjects with HPS who had ILD but not subjects without lung disease or normal cont
124 at proved effective in correctly identifying ILD patients in the training and validation data sets.
125 = 33), patients with alternative idiopathic ILDs (a-ILD; n = 41), and healthy control subjects (n =
131 ydrogenase [COX/SDH]-ratio) was depressed in ILD (median = 0.10,) compared with controls (0.12, p < 0
136 our understanding of mechanisms involved in ILD and thereby aid in identification of new therapeutic
140 ent predicts TFS and hospitalization risk in ILD and is associated with decreased levels of a key cir
142 2) assess the reversibility of inflammatory ILD following anti-TNF therapy known to resolve TNF-Tg i
145 case report forms: local site investigators, ILD experts at the National Data Coordinating Center (ND
148 f interaural time and level differences (ITD/ILD), which are the timing and intensity differences of
149 l information was analyzed in terms of ITDs, ILDs, and interaural coherence, both for whole stimuli a
150 Cs between the readers and the deep learning ILD contours ranged from 0.74 to 0.75, whereas the media
151 l differences in the timing (ITD) and level (ILD) of impinging sounds carry critical information abou
154 onwide, population-based SSc cohort.Methods: ILD was assessed prospectively in the Norwegian SSc (Nor
160 ioral ILD sensitivity (in humans) and neural ILD sensitivity (in single neurons of the chinchilla aud
162 adulthood, allows for study of biomarkers of ILD in a homogeneous population at near-certain risk of
163 ky-Pudlak syndrome (HPS), a genetic cause of ILD in early adulthood, allows for study of biomarkers o
166 audit of patients with a prior diagnosis of ILD admitted to the hospital with COVID-19 between March
167 rred for lung transplant with a diagnosis of ILD and is associated with a marked increase in mortalit
168 dication, 52 participants had a diagnosis of ILD during 75,232 person-years (median, 12.2 yr) of foll
172 < 0.001).Conclusions: An undiagnosed form of ILD may be present in greater than 1 in 6 older first-de
174 understanding of several different forms of ILD, including neuroendocrine cell hyperplasia of infanc
175 high molecular and cellular heterogeneity of ILD, common protein regulations are observed, even acros
176 nt strategies.Objectives: Evaluate impact of ILD in a unique, nationwide, population-based SSc cohort
177 classification, diagnosis, and management of ILD in children, focusing on neonates and infants under
179 mpared with the outputs of a simple model of ILD processing with a single free parameter, the duratio
182 (P = 0.03).Conclusions: The mere presence of ILD at baseline appears to affect outcome in SSc, sugges
183 e coding can account for the preservation of ILD sensitivity despite even extreme temporal degradatio
184 osis is challenging because of the rarity of ILD and the fact that the presenting symptoms of ILD oft
185 as were associated with an increased rate of ILD hospitalization (adjusted hazard ratio, 2.6 per 1-SD
186 re also associated with an increased rate of ILD-specific death (adjusted hazard ratio, 2.3; 95% conf
188 uation areas are associated with the risk of ILD hospitalization and mortality in the general populat
190 and the fact that the presenting symptoms of ILD often overlap those of common respiratory disorders.
191 learning-based method to depict worsening of ILD based on lung shrinkage detection from elastic regis
194 ry and inhibitory inputs for the encoding of ILDs, human and animal behavioral ILD sensitivity is rob
198 Indian origin living in India with new-onset ILD (27 centers, 19 Indian cities, March 2012-June 2015)
199 ty pneumonitis was the most common new-onset ILD in India, followed by CTD-ILD and idiopathic pulmona
201 f home oxygen therapy in adults with COPD or ILD but also highlight the need for additional research
202 nts with COPD (moderate-quality evidence) or ILD (low-quality evidence) with severe chronic resting h
203 nts with COPD (moderate-quality evidence) or ILD (low-quality evidence) with severe exertional hypoxe
204 nalyses that the prevalence of either ILA or ILD differed between the 46 relatives with FPF and the 5
205 sensitivity to parametrically varied ITD or ILD cues was measured using fMRI during spatial and nons
206 orded IC neurons sensitive to either ITDs or ILDs in anesthetized guinea pig, before, during, and fol
207 proved successful in predicting SSc patient ILD status with a high degree of success (>82% correct c
208 we study the synaptic currents that process ILD in vivo and use stimuli in which ILD varies around a
210 nset ILDs in India by creating a prospective ILD using multidisciplinary discussion (MDD) to validate
214 k factors and autoantibodies can identify RA-ILD and if the addition of investigational biomarkers is
216 with rheumatoid arthritis-associated ILD (RA-ILD; n = 33), patients with alternative idiopathic ILDs
217 to elucidate the genesis of inflammatory RA-ILD, we aim to achieve the following: 1) characterize th
218 findings may facilitate identification of RA-ILD at an earlier stage, potentially leading to decrease
220 CD21(+)/CD23(-) B cells in the genesis of RA-ILD, which exist in a previously unknown, reversible, pr
221 nce of clinically evident and subclinical RA-ILD on computed tomography scan in two independent RA co
222 rum of clinically evident and subclinical RA-ILD) and 76 ACR subjects with research or clinical scans
224 e antibodies was strongly associated with RA-ILD (areas under the curve, 0.88 for BRASS and 0.89 for
229 ess CT images from patients with SSc-related ILD.Supplemental material is available for this article.
237 nesis of fibrosis in SSc-associated ILD (SSc-ILD) involves cellular injury, activation/differentiatio
239 provided the MCID estimates for FVC% in SSc-ILD based changes at 12 months from baseline in two clin
240 neumonia pattern is commonly observed in SSc-ILD, whereas IPF is defined by usual interstitial pneumo
241 enetic risk, and distinctive features of SSc-ILD and identification of robust prognostic biomarkers a
243 se state such as the risk or presence of SSc-ILD, the activity of lung involvement and the likelihood
246 ough appropriately treated patients with SSc-ILD have better chances of stabilization and survival, a
250 imely recognition of children with suspected ILD and initiation of appropriate diagnostic evaluations
252 and modeling data collectively suggest that ILD sensitivity depends on binaural integration of excit
256 ntegration potentiates a unique role for the ILD system in spatial hearing that may be of particular
259 ordings from the same neuron showed that the ILD tuning of the spikes was sharper than that of the EP
261 n auditory cortex believed to be integral to ILD processing (excitatory from one ear, inhibitory from
265 ts with progressive fibrosing unclassifiable ILD could benefit from pirfenidone treatment, which has
266 rs) had progressive fibrosing unclassifiable ILD, a percent predicted forced vital capacity (FVC) of
272 process ILD in vivo and use stimuli in which ILD varies around a constant average binaural level (ABL
273 cell types are explained by a model in which ILDs are computed within separate frequency channels and
276 nd Main Results: Data from 349 patients with ILD across Europe were included, of whom 161 were admitt
277 st and during exercise in both patients with ILD and patients with COPD than in control subjects.
278 2.27; 1.39-3.71).Conclusions: Patients with ILD are at increased risk of death from COVID-19, partic
282 sine were markedly elevated in patients with ILD compared with control subjects with receiver operati
285 ectives: To assess outcomes in patients with ILD hospitalized for COVID-19 versus those without ILD i
286 is a predictor of mortality in patients with ILD referred for lung transplantation in an Australian c
288 ter prospective study included patients with ILD with a nondefinite usual interstitial pneumonia patt
291 ry-mechanical relationships in patients with ILD, patients with COPD, and healthy control subjects (n
295 e 5-year follow-up HRCT, the proportion with ILD events (endpoint met or radiographic ILA progression
296 patterned spectral cues in combination with ILDs give rise to the topographic map of azimuthal audit
298 ndertaken and compared with patients without ILD, obtained from the ISARIC4C (International Severe Ac
299 spitalized for COVID-19 versus those without ILD in a contemporaneous age-, sex-, and comorbidity-mat