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1 monary dysplasia (BPD; also known as chronic lung disease).
2 monia, spinal cord abscess, and interstitial lung disease).
3 ecular mechanisms that underlie inflammatory lung disease.
4 mplicated and patients often develop chronic lung disease.
5 romising therapeutic target for inflammatory lung disease.
6 2-5 years from this progressive interstitial lung disease.
7 ons to CFTR, leads to severe and progressive lung disease.
8 C/TLC in identifying features of obstructive lung disease.
9  consolidations in patients with more severe lung disease.
10 tcomes in hypercapnic patients with advanced lung disease.
11 ociations among air pollution, diabetes, and lung disease.
12 ertension, diabetes, and chronic obstructive lung disease.
13 l therapeutic targets in the treatment of CF lung disease.
14 ther deteriorated in the presence of chronic lung disease.
15  (LBW) are risk factors for neonatal chronic lung disease.
16 SeV- and influenza A virus-induced long-term lung disease.
17 r clinical management of COVID-19 associated lung disease.
18 set, and progression of cystic fibrosis (CF) lung disease.
19 veries that change the natural history of CF lung disease.
20  the periphery to center progression of this lung disease.
21 ive stress, consistent with a key role in CF lung disease.
22 ons, including growth impairment and chronic lung disease.
23 ry vascular dilatation on CE, and absence of lung disease.
24 duce CTSS activity and counter smoke-induced lung disease.
25 f lung US SWE for evaluation of interstitial lung disease.
26 and drastically ameliorated STING-associated lung disease.
27 ay provide opportunities for intervention in lung disease.
28 ers, including among those without prevalent lung disease.
29 t, HIV viral load, or HIV-associated chronic lung disease.
30 pear to influence the development of chronic lung disease.
31 th CF and from 1 patient with non-CF chronic lung disease.
32 sed to hyperoxia who later developed chronic lung disease.
33 (SAVI), affects children and leads to severe lung disease.
34 ution in individuals with underlying chronic lung disease.
35 nary Fibrosis (IPF), a progressive and fatal lung disease.
36 ed health effects, particularly interstitial lung disease.
37 ulmonary dysplasia (BPD), a neonatal chronic lung disease.
38 n important pathogenic component of fibrotic lung disease.
39 and study participants with any interstitial lung disease.
40 nal repair play a role in the development of lung disease.
41 tic target against premalignancy and chronic lung disease.
42 ontribute to dysregulated host defense in CF lung disease.
43 putum samples of individuals with underlying lung disease.
44 infections and the progression of structural lung disease.
45 cal thromboinflammatory effector cells in CF lung disease.
46 n) from 17 patients with no, mild, or severe lung disease.
47 ies and findings suspicious for interstitial lung disease.
48 ractive target for the treatment of fibrotic lung diseases.
49 tic targets in the management of obstructive lung diseases.
50 goes on to drive development of most chronic lung diseases.
51 n is essential for recovery from devastating lung diseases.
52 in the diagnosis and treatment of a range of lung diseases.
53 ic tools to treat patients with a variety of lung diseases.
54 nditions such as hypertension, diabetes, and lung diseases.
55 e central to the pathogenesis of a number of lung diseases.
56  airways and lung samples from patients with lung diseases.
57 gs, is a component of many chronic and acute lung diseases.
58 owing the in vitro modeling of a plethora of lung diseases.
59 ful in preventing alloimmune-driven fibrotic lung diseases.
60 h symptoms that overlap infectious and other lung diseases.
61 hologies are prominent in neonatal and adult lung diseases.
62 harmacologic target for inflammation-related lung diseases.
63 e pathogenesis of allergy, asthma, and other lung diseases.
64 ding diagnosis and prognosis in interstitial lung diseases.
65 stic fibrosis and other pre-existing chronic lung diseases.
66 alidate this approach across a wide range of lung diseases.
67 isms that mediate distinct chronic postviral lung diseases.
68  and sepsis and can trigger exacerbations of lung diseases.
69 ncreased susceptibility to acute and chronic lung diseases.
70 lopment of therapeutics to treat obstructive lung diseases.
71 athophysiology of emphysema and inflammatory lung diseases.
72 ty in patients with severe acute and chronic lung diseases.
73 gy could inform our understanding of complex lung diseases.
74 ase (COPD) and asthma remain prevalent human lung diseases.
75 l facilitate interpretation of risk loci for lung diseases.
76 D (Global Initiative for Chronic Obstructive Lung Disease) 2020 Report aims to provide a nonbiased re
77  117 acute hospitalizations with obstructive lung disease, 227 acute hospitalizations with pneumonia,
78 ease (11.8% versus 6.0%, p = 0.006), chronic lung disease (28.0% versus 19.3%, p = 0.007), diabetes (
79 [SD], 62.4 years +/- 12.9) with interstitial lung disease and 30 healthy subjects (women, 16; men, 14
80                                    End-stage lung disease and advanced cardiac conditions are frequen
81  were undergoing evaluation for interstitial lung disease and had had samples obtained by clinically
82 o distinct stages of progression of COVID-19 lung disease and highlights the need for peripheral bloo
83 ttee of experts in the field of interstitial lung disease and HP using the GRADE (Grading of Recommen
84 tabolism have been described during fibrotic lung disease and in murine models of lung fibrosis.
85 ons adds to our evolving understanding of CF lung disease and may help guide antibiotic therapies tar
86 ivacaftor was associated with improvement in lung disease and nutritional status in patients who tole
87 he nivolumab group (one each of interstitial lung disease and pneumonitis) and three in the chemother
88 escribe 2 patients presenting with end-stage lung disease and significant aortic stenosis who were su
89 ction and can be used to define the basis of lung disease and test immune and antiviral-based counter
90 jective information used in the diagnosis of lung diseases and monitoring lung health.
91  with minimal side effects a wide variety of lung diseases and possibly other acute respiratory syndr
92 acute myocardial infarction and interstitial lung disease) and one (<1%) in the placebo group (arrhyt
93 lactate dehydrogenase level, distribution of lung disease, and chest radiography score at hospital pr
94  obstructive pulmonary disease, interstitial lung disease, and coronary artery disease.
95                           Older age, chronic lung disease, and hypertension were associated with seve
96 en groups by age (mean, ~79), heart failure, lung disease, and influenza and pneumococcal vaccine upt
97 ry fibrosis (IPF) is a progressive and fatal lung disease, and its molecular pathogenesis remains poo
98 minal pain, colitis, hepatitis, interstitial lung disease, and jaundice, and grade 4 cholestasis, and
99 ng, cyanotic heart disease, active perinatal lung disease, and preparation or recovery from a cardiac
100 153S mice that lack adaptive immunity had no lung disease, and T-cell receptor beta chain (Tcrb)(-/-)
101 failure, stroke, asthma, chronic obstructive lung disease, and type 2 diabetes mellitus.
102 e [aOR 3.2, 95%CI 1.4-7.0, p=0.004], chronic lung disease [aOR 2.5, 95%CI 1.2-5.2, p=0.018], obesity
103  that macrophage contributions to CF-related lung disease are primarily shaped by their environment.
104                                              Lung diseases are a leading cause of mortality worldwide
105 acterized animal models of postviral chronic lung diseases are necessary to study the underlying mech
106 ar epithelial turnover observed with chronic lung diseases are unknown.
107 rmalities, such as emphysema and restrictive lung diseases, are frequently observed in patients with
108 in large animals to enable modeling of human lung disease as well as cell-based therapeutic intervent
109 e pulmonary disease (COPD) is a debilitating lung disease associated with cigarette smoking.
110    Allergic asthma is a chronic inflammatory lung disease associated with increased cytokine secretio
111 severe bronchopulmonary dysplasia, a chronic lung disease associated with preterm birth, which is cha
112 -hospital mortality in fibrotic interstitial lung disease-associated mechanical ventilation when view
113         Among participants without prevalent lung disease, associations were attenuated but were cons
114        All 14 patients showed first signs of lung disease at a median onset of 1.5 years of age.
115  used to successfully investigate airway and lung diseases at single-cell resolution.
116 ith pulmonary vascular pathology and chronic lung diseases, but it remains unclear whether endothelia
117 alled the Pi*ZZ genotype, causes a liver and lung disease called alpha-1 antitrypsin deficiency.
118 airways of smokers and patients with chronic lung disease, can cause pneumonia and sepsis and can tri
119 tigation of pathologies such as interstitial lung disease, cancer and coronavirus disease 2019 (COVID
120 2018) and the Canadian Cohort of Obstructive Lung Disease (CanCOLD), which involved 1272 participants
121  of diabetes, hypertension, stroke, cancers, lung diseases, cardiovascular diseases, and cognitive im
122  higher prevalence of chronic kidney, liver, lung diseases, cardiovascular diseases, type 2 diabetes,
123     In this study, we cross-analyzed chronic lung disease caused by infection with Sendai virus (SeV)
124  is only reserved for patients with advanced lung disease caused by severe AAT deficiency.
125 ystem disorder, but progressive inflammatory lung disease causes the greatest burden of morbidity and
126 iopathic pulmonary fibrosis (IPF) are severe lung diseases causing irreversible lung damage and prema
127 ) conducted in 39 UK specialist interstitial lung disease centers between April 2015 (first patient v
128 t 65 pulmonary hypertension and interstitial lung disease centres in 19 countries to evaluate the eff
129                                 Interstitial lung disease characteristics, demographics, and ventilat
130  pulmonary hypertension (PH) is an infantile lung disease characterized by aberrant angiogenesis and
131 he major cause of morbidity and mortality is lung disease characterized by inflammation and infection
132  (IPF) is a chronic progressive interstitial lung disease characterized by patchy scarring of the dis
133 ronchopulmonary dysplasia is a heterogeneous lung disease characterized by regions of cysts and fibro
134 pathic pulmonary fibrosis (IPF) is a complex lung disease characterized by scarring of the lung that
135                       Childhood interstitial lung disease (chILD) comprises a spectrum of rare diffus
136          Children's interstitial and diffuse lung disease (chILD) is a rare heterogenous group of con
137 ren with children's interstitial and diffuse lung disease (chILD) to improve diagnostic approaches, i
138 tly older; more frequently presented chronic lung disease, chronic heart failure, prior endocarditis,
139 he Global Initiative for Chronic Obstructive Lung Disease classification system (P = .0015), more fre
140               In those without known chronic lung disease (CLD) (HR, 3.09; P = .024) and those withou
141                                      Chronic lung disease (CLD) has been reported among African child
142                                      Chronic lung disease (CLD) is a common co-morbidity for HIV-posi
143 osis and in human subjects with interstitial lung disease compared to that in control healthy subject
144 17 Global Initiative for Chronic Obstructive Lung Disease criteria.
145 ations into the specific mechanisms by which lung disease develops in RA will be crucial for the deve
146 ue for sampling lung tissue for interstitial lung disease diagnosis.
147 the clinical utility of TBLC in interstitial lung disease diagnostic algorithms.
148 of people worldwide with incurable end-stage lung disease die because of inadequate treatment options
149 oleiomyomatosis (LAM) is a rare fatal cystic lung disease due to bi-allelic inactivating mutations in
150 crophage activation, and the pathogenesis of lung disease due to CS exposure.
151                We confirmed the induction of lung disease enhancement by vaccinations with low antige
152 gainst RSV infection but also induced severe lung disease enhancement in vaccinated children.
153  participants with any grade of interstitial lung disease (F1-F3).
154 ies cell types that are directly affected by lung disease genes and respiratory viruses.
155   Granulomatous and lymphocytic interstitial lung disease (GLILD) is a life-threatening complication
156 en Global Initiative for Chronic Obstructive Lung Disease (GOLD) 1 and GOLD 4 COPD was reduced by 13.
157 98 Global Initiative for Chronic Obstructive Lung Disease (GOLD) 1-4 patients and 3,479 controls from
158 ng Global initiative for chronic Obstructive Lung Disease (GOLD) criteria.
159 by Global Initiative for Chronic Obstructive Lung Disease (GOLD) stage (GOLD 0, no COPD; GOLD 1, mild
160 city of 81% for differentiating interstitial lung disease grades F0-F2 from F3.
161 r to suboptimal clinical outcomes in various lung disease groups.
162  extensive pulmonary fibrosis or restrictive lung disease has occurred.
163 tem, where circadian rhythms in inflammatory lung disease have been appreciated since ancient times.
164 e interval, 3.39-12.2) for acute obstructive lung disease hospitalizations, 2.03 (1.43-2.88) for acut
165                 During the progression of CF lung disease, however, the emergence of multidrug antimi
166 D (Global Initiative for Chronic Obstructive Lung Disease II-IV) who were carefully characterized (in
167 ine progression toward clinical interstitial lung disease (ILD) among subjects in a longitudinal coho
168 ) is prevalent in patients with interstitial lung disease (ILD) and may reflect immunologic activatio
169 as the current gold standard-in interstitial lung disease (ILD) cases requiring histology remains con
170 ase (COVID-19) on patients with interstitial lung disease (ILD) has not been established.Objectives:
171                                 Interstitial lung disease (ILD) is fast approaching chronic obstructi
172 identification of more advanced Interstitial Lung Disease (ILD) patterns, few have tackled ILA, which
173                      Rationale: Interstitial lung disease (ILD) represents a major challenge in syste
174 nary disease (COPD), asthma and interstitial lung disease (ILD), and individual cardiovascular diseas
175 F) are at an increased risk for interstitial lung disease (ILD), the risk among relatives of sporadic
176 re available for unclassifiable interstitial lung disease (ILD), which is characterised by progressiv
177 rtality, even in the absence of Interstitial Lung Disease (ILD).
178  25% to 30% develop progressive interstitial lung disease (ILD).
179 ents as pulmonary hemorrhage or interstitial lung disease (ILD).
180 ve pulmonary disease (COPD) and interstitial lung disease (ILD).Methods: The multidisciplinary panel
181 fections (EAR, 10.6; SMR, 3.9), interstitial lung disease (ILD; EAR, 9.7; SMR, 22.1), and adverse eve
182 round Longitudinal follow-up of interstitial lung diseases (ILDs) at CT mainly relies on the evaluati
183 ung diseases such as asthma and interstitial lung diseases (ILDs), including idiopathic pulmonary fib
184                      Lung cancer and chronic lung diseases impose major disease burdens worldwide and
185 sk factors, and potential pathophysiology of lung disease in individuals with established RA.
186 cial component in the treatment of end-stage lung disease in infants.
187 y predispose individuals to be vulnerable to lung disease in later life.
188 e immunodeficiency, leading to virus-induced lung disease in mice.
189 N153S relies primarily on T cells to promote lung disease in mice.
190 he hypothesis that impaired lung function or lung disease in midlife is associated with greater risk
191 ver, a single dose conferred protection from lung disease in most of the vaccinated hamsters within a
192 important contributors to the development of lung disease in patients with RA.
193 gic and functional worsening of interstitial lung disease in patients with systemic sclerosis.
194  of this study was to expand knowledge about lung disease in STAT3-HIES.
195                                              Lung disease in STING N153S mice developed independently
196                                  Spontaneous lung disease in STING N153S mice develops independently
197 splant candidacy for patients with end-stage lung disease in the setting of severe aortic stenosis, l
198  could herald the development of significant lung disease in these susceptible individuals.
199 s a fatal and incurable form of interstitial lung disease in which persistent injury results in scar
200 ssociated with the progression of structural lung disease in young children with CF.
201 ociations between Aspergillus infections and lung disease in young children with CF.Methods: Longitud
202 terium, is increasingly prevalent in chronic lung disease, including cystic fibrosis, and infections
203  the two pivotal features of cystic fibrosis lung disease, inflammation and infection, and thus repre
204                   These data suggest chronic lung disease influences the microbiota of sputum in pati
205 erm birth, congenital heart disease, chronic lung disease, intensive care unit admission, and ventila
206  lung function in patients with interstitial lung disease is accompanied by epithelial remodeling and
207                         Cystic fibrosis (CF) lung disease is characterized by an inflammatory respons
208                                           CF lung disease is driven by innate immune dysfunction and
209 receptors in mice helps explain why COVID-19 lung disease is greater in the elderly and people with p
210                     The severity of COVID-19 lung disease is higher in the elderly and people with pr
211                                              Lung disease is independently associated with cardiovasc
212 (IPF), a fatal and irreversible interstitial lung disease, is predicted by the circulating blood conc
213           Underlying cardiovascular disease, lung disease, kidney disease, diabetes, immunosuppressio
214  fibrosis-related diabetes (CFRD) worsens CF lung disease leading to early mortality.
215 vascular remodeling (PVR) are common in many lung diseases leading to right ventricular dysfunction a
216 ASM with the pathogenesis of T(H) 1-directed lung diseases like cystic fibrosis and acute lung injury
217 for acquisition of TCD included pre-existing lung diseases, lower GI endoscopy and antibiotics.
218 living with HIV have high burdens of chronic lung disease, lung cancers, and pulmonary infections des
219 dverse events were worsening of interstitial lung disease (main study: six [8%] of 73 in the riocigua
220 cGAS-STING pathway over-activation can drive lung disease, making this pathway a promising therapeuti
221  analyze the association of FSTL-1 SNPs with lung disease.Methods: FSTL-1 hypomorphic (FSTL-1 Hypo) m
222 of immune function and the development of CF lung disease.Methods: We performed single-cell RNA seque
223 related phenotypes in a cystic fibrosis-like lung disease model (i.e., Scnn1b-Tg-positive [Tg+]) mous
224 fidence interval, 1.14-2.19) and obstructive lung disease (multivariable-adjusted odds ratio, 1.33; 9
225  in many situations including high altitude, lung disease, obstructive sleep apnea, and age-related C
226  IA among recipients with underlying chronic lung diseases (odds ratio [OR] = 7.26; 95% confidence in
227 pulmonary adenocarcinoma (OPA), a neoplastic lung disease of sheep.
228 osis (IPF) is a rare and devastating chronic lung disease of unknown etiology.
229 a progressive and heterogeneous interstitial lung disease of unknown origin with a low survival rate.
230      The primary outcome was the severity of lung disease on admission chest radiographs, measured by
231 eristics associated with escalation included lung disease, ongoing angina, and periprocedural major a
232 rs that can distinguish active TB from other lung diseases (OPD), and that could be further evaluated
233 tions, regardless of diagnosis (interstitial lung disease or chronic obstructive pulmonary disease).
234 5; 95% CI = 1.24-8.03), and comorbid chronic lung disease (OR = 3.87; 95% CI = 1.52-9.83).
235 1.3; 95% CI: 1.1, 1.6, P = .01), and chronic lung disease (OR, 1.3; 95% CI: 1.0, 1.6; P = .02).
236                        Patients with chronic lung disease (other than asthma) were excluded.
237          Affected patients developed chronic lung disease over time (47% after 40 years of follow-up)
238 t, dehydration, hepatotoxicity, interstitial lung disease, pancytopenia, and sepsis [n=1 each]), and
239  causative agent of the devastating COVID-19 lung disease pandemic.
240              The potential impact on chronic lung disease pathogenesis needs further investigation.
241  the lung, sparking exploration of clocks in lung disease pathophysiology.
242 s of a large cohort of fibrotic interstitial lung disease patients from the perspective of an acute r
243  of 10 patients (1.2% of the 760 restrictive lung disease patients transplanted in the same time peri
244 gnificant mortality in fibrotic interstitial lung disease patients undergoing mechanical ventilation.
245 infection, none have fully recapitulated the lung disease phenotypes seen in humans who have been hos
246 estigators reported 20 cases of interstitial lung disease, pneumonitis, or organising pneumonia, incl
247 d an effect modification whereby obstructive lung disease prevalence among persons with limited smoki
248                   The unadjusted obstructive lung disease prevalence was similar in HIV-infected (23.
249    Baseline comorbidities (diabetes, chronic lung disease, previous acute HF) and echocardiographic f
250 dmission included diabetes mellitus, chronic lung disease, previous acute HF, grade III or IV aortic
251 rence in change in King's Brief Interstitial Lung Disease Questionnaire (K-BILD) score at 24 weeks.Me
252 Questionnaire, and King's Brief Interstitial Lung Disease questionnaire scores).
253 ighly active antiretroviral therapy (HAART), lung disease remains common in human immunodeficiency vi
254               They suffered from restrictive lung disease requiring noninvasive mechanical ventilatio
255 ity and findings suspicious for interstitial lung disease, respectively.
256 pleted a questionnaire regarding obstructive lung diseases, respiratory symptoms, potential risk fact
257  bone marrow chimeric mice were assessed for lung disease severity and survival.
258 thelial cells in adult mice produces chronic lung disease sharing key features with IPF including pro
259 e and its risk factors, diabetes, underlying lung disease, smoking, immunosuppressed condition, and b
260 and former Global Initiative for Obstructive Lung Disease stage 0 smokers predicted structural and ph
261 defined as Global Initiative for Obstructive Lung Disease stage 0).
262 in Global Initiative for Chronic Obstructive Lung Disease stage 4 versus stage 1 COPD (P < 0.0001).
263 to Global Initiative for Chronic Obstructive Lung Disease stage higher than 1 (odds ratio = 1.96 [95%
264 17 Global Initiative for Chronic Obstructive Lung Disease stage II subjects with COPD and as controls
265 th Global Initiative for Chronic Obstructive Lung Disease stage II-IV COPD and persistent symptoms an
266 as Global Initiative for Chronic Obstructive Lung Disease stage II-IV were enrolled.
267 on Global Initiative for Chronic Obstructive Lung Disease stage IV COPD lungs with TLOs.Measurements
268  been implicated in the pathology of chronic lung diseases such as asthma and interstitial lung disea
269  mucus biology and improve the management of lung diseases such as asthma, cystic fibrosis, and chron
270 ity, especially in patients with preexisting lung diseases such as asthma.
271 ssociated protease with elevated activity in lung diseases such as bacterial infection and alpha-1 an
272 osis and inflammation that underlies chronic lung diseases such as idiopathic pulmonary fibrosis (IPF
273 ulation and has been associated with several lung diseases, such as asthma, pulmonary fibrosis, and l
274  variables included sex, chronic obstructive lung disease, symptom duration, neutrophil count, C-reac
275                               Pneumonia is a lung disease that can cause respiratory failure and hypo
276                      In concert, the chronic lung disease that develops after Sendai virus infection
277 e pulmonary disease (COPD) is a debilitating lung disease that is currently the third leading cause o
278 nts with COPA syndrome develop arthritis and lung disease that presents as pulmonary hemorrhage or in
279 IPF) are two pathologically distinct chronic lung diseases that are associated with cigarette smoking
280 c dysfunction that may contribute to chronic lung diseases that arise in association with TLO formati
281  prevent deregulated tissue cell activity in lung diseases that involve fibrosis and remodeling.
282 sponse to AA protected against S. pneumoniae lung disease, the IL-6 deficiency abrogated the protecti
283 s might be valuable in patients with certain lung diseases, the goal was to find out if ABC-like cell
284 ding and management of lung inflammation and lung disease throughout the natural history of RA.
285 bstructive pulmonary disease or interstitial lung disease transplant recipients is associated with al
286            At postnatal days 12 and 18, mild lung disease was evident by histopathologic analysis tog
287                     Severity of interstitial lung disease was graded as none (healthy lung [F0]), mil
288 currence of radiation-associated cardiac and lung disease was rare and not influenced by the fraction
289 hat coronary artery disease, but not chronic lung disease, was associated with death among hospitaliz
290         Participants with prevalent clinical lung disease were excluded.
291                                Patients with lung disease were less likely to receive coronary revasc
292            Emphysema and chronic obstructive lung disease were previously identified as major risk fa
293                                              Lung diseases were also assessed as dichotomous variable
294 nction decline and susceptibility to chronic lung diseases, which are the third leading cause of deat
295  distress syndrome (ARDS) is an inflammatory lung disease with a high morbidity and mortality rate, f
296 fibrosis (IPF) is a progressive interstitial lung disease with a median survival of 3 years after dia
297 ic pulmonary fibrosis (IPF) is a progressive lung disease with a poor prognosis.
298 nary fibrosis (IPF) is a chronic progressive lung disease with limited therapeutic options and poor p
299 mune response leading to long-term postviral lung diseases with features of asthma and related progre
300                Research on acute and chronic lung diseases would greatly benefit from reproducible av

 
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