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1 onic kidney disease, and chronic obstructive pulmonary disease).
2 atment for patients with chronic obstructive pulmonary disease.
3 ion, and associated with chronic obstructive pulmonary disease.
4 dification by asthma and chronic obstructive pulmonary disease.
5 herapeutic approaches in chronic obstructive pulmonary disease.
6 th acute exacerbation of chronic obstructive pulmonary disease.
7 lity to NTM infection and its progression to pulmonary disease.
8 ted yet in patients with chronic obstructive pulmonary disease.
9 the main risk factor for chronic obstructive pulmonary disease.
10 raining in patients with chronic obstructive pulmonary disease.
11 cystic fibrosis (CF) and chronic obstructive pulmonary disease.
12 dicate an early stage of chronic obstructive pulmonary disease.
13 cal history of asthma or chronic obstructive pulmonary disease.
14 in patients with severe chronic obstructive pulmonary disease.
15 d cohort free of clinical cardiovascular and pulmonary disease.
16 matory diseases, such as chronic obstructive pulmonary disease.
17 no previous spirometry testing or diagnosed pulmonary disease.
18 y developmental phase of chronic obstructive pulmonary disease.
19 76 men) free of prevalent cardiovascular and pulmonary disease.
20 or in the development of chronic obstructive pulmonary disease.
21 s a syndromic condition including late-onset pulmonary disease.
22 patients suffering from chronic obstructive pulmonary disease.
23 cerbations of asthma and chronic obstructive pulmonary disease.
24 msubsp.hominissuis" is an important cause of pulmonary disease.
25 om cirrhosis, cancer, or chronic obstructive pulmonary disease.
26 mans from zoonotic sources and causes severe pulmonary disease.
27 or agonist used to treat chronic obstructive pulmonary disease.
28 airway diseases, such as chronic obstructive pulmonary disease.
29 both cystic fibrosis and chronic obstructive pulmonary disease.
30 l lung pathologies, e.g. chronic obstructive pulmonary disease.
31 iew the contributions of the inflammasome to pulmonary diseases.
32 the lipidome for future MALDI-MSI studies of pulmonary diseases.
33 marily because of cardiovascular and chronic pulmonary diseases.
34 the effects of therapeutic interventions in pulmonary diseases.
35 velopment, injury, and repair as well as key pulmonary diseases.
36 ired goal in patients with acute and chronic pulmonary diseases.
37 erous human inflammatory diseases, including pulmonary diseases.
38 included diabetes (21%), chronic obstructive pulmonary disease (12%), and immunosuppression (3%).
39 y disease (15.6%-22.3%), chronic obstructive pulmonary disease (14.4%-20.1%), anemia (12.4%-20.4%), c
40 abetes mellitus (29.5%), chronic obstructive pulmonary disease (16.0%), and a mean logistic EuroSCORE
41 e inception of asthma or chronic obstructive pulmonary disease, (2) inflammatory phenotyping, (3) exa
42 ilty (29%), frailty with chronic obstructive pulmonary disease (25%), and frailty with diabetes melli
43 8% versus 12%, P<0.001), chronic obstructive pulmonary disease (5% versus 3%, P=0.004), urgent/emerge
45 evalent diseases such as chronic obstructive pulmonary disease, acquired rhinosinusitis, pancreatitis
46 sing MRI contrast agent for the diagnosis of pulmonary diseases affecting the surface of the respirat
47 mitation compatible with chronic obstructive pulmonary disease affects almost one-third of patients w
48 excessive alcohol, smoking, hyperthyroidism, pulmonary disease, air pollution, and possibly excessive
49 excessive alcohol, smoking, hyperthyroidism, pulmonary disease, air pollution, heart failure, and pos
50 lure, moderate-to-severe chronic obstructive pulmonary disease, airway patency problems, and prolonge
51 tion; moderate to severe chronic obstructive pulmonary disease; airway patency problems; or prolonged
52 c pulmonary fibrosis and chronic obstructive pulmonary disease, although the factors that regulate ea
53 the higher prevalence of chronic obstructive pulmonary disease among Puerto Ricans and Cubans was lar
54 59, 95 % CI: 1.33-1.90), chronic obstructive pulmonary disease and bronchiectasis (HR 1.55, 95 % CI:
55 ic lung disease, such as chronic obstructive pulmonary disease and cystic fibrosis, exhibited increas
56 ex-smokers with combined chronic obstructive pulmonary disease and heart failure with reduced left ve
58 driceps of patients with chronic obstructive pulmonary disease and intensive care unit-acquired weakn
59 varied phenotypically as chronic obstructive pulmonary disease and IPF and suggest that these hubs ma
60 f airflow obstruction in chronic obstructive pulmonary disease and may precede emphysema development.
62 any patients with chronic severe obstructive pulmonary disease and other advanced lung disorders.
63 n central Appalachia for chronic obstructive pulmonary disease and pneumoconiosis; widely dispersed t
64 usceptibility to develop chronic obstructive pulmonary disease and pulmonary function levels, includi
65 eumatoid arthritis, asthma, atherosclerosis, pulmonary diseases and Crohn's disease as hubs and thus
66 , stroke, pneumonia, and chronic obstructive pulmonary disease) and a surgical diagnosis (hip fractur
67 c heart disease, stroke, chronic obstructive pulmonary disease, and cancers (liver, stomach, and lung
69 cerebrovascular disease, chronic obstructive pulmonary disease, and hemoglobin, was a powerful predic
70 emia occurs in advanced hepatic, cardiac and pulmonary disease, and in urea cycle enzyme deficiencies
71 atory distress syndrome, chronic obstructive pulmonary disease, and interstitial lung diseases such a
73 asthma, 298,751 cases of chronic obstructive pulmonary disease, and more than 1.1 million cases of al
74 rease) with respiratory, chronic obstructive pulmonary disease, and pneumonia mortality, with risk ra
77 participants, those with chronic obstructive pulmonary disease, and those with more than 35 pack-year
79 to 45%) of patients with chronic obstructive pulmonary disease are never-smokers, most genetic suscep
80 onary fibrosis (IPF) and chronic obstructive pulmonary disease are usually studied in isolation, and
81 phages (AM) are found in chronic obstructive pulmonary disease, asthma, cystic fibrosis, and adenosin
82 including renal disease, chronic obstructive pulmonary disease, atrial fibrillation, heart disease, a
84 to the ED were more likely to be black, have pulmonary disease, be insured by the Centers for Medicai
85 levated in patients with chronic obstructive pulmonary disease but more markedly in patients with ICU
86 patients with asthma and chronic obstructive pulmonary disease, but are not recommended for those wit
87 rticularly in asthma and chronic obstructive pulmonary disease, but their potential role in patients
88 roke, arthritis, asthma, chronic obstructive pulmonary disease, cancer, weak/failing kidneys, diabete
89 p (atrial septal defect, chronic obstructive pulmonary disease, chest pain, diverticulitis, enteroves
90 with severe/very severe chronic obstructive pulmonary disease, chronic bronchitis, two or more exace
91 Heart Association class, chronic obstructive pulmonary disease, chronic kidney disease, N-terminal-pr
92 cerebrovascular disease, chronic obstructive pulmonary disease, chronic renal failure, previous invas
93 asthma were as follows: chronic obstructive pulmonary disease (COPD) (13.4% vs 3.1%), depression (17
95 expression that occur in chronic obstructive pulmonary disease (COPD) after corticosteroid treatment
96 s (ICS) in patients with chronic obstructive pulmonary disease (COPD) and a history of exacerbations.
97 nts, human patients with chronic obstructive pulmonary disease (COPD) and amyotrophic lateral scleros
98 n lungs of patients with chronic obstructive pulmonary disease (COPD) and asthma compared to controls
99 characteristics of both chronic obstructive pulmonary disease (COPD) and asthma, named asthma-COPD o
100 lung diseases including chronic obstructive pulmonary disease (COPD) and cystic fibrosis (CF), but l
103 mulant for patients with chronic obstructive pulmonary disease (COPD) and metabolic alkalosis, but no
104 in patients with stable chronic obstructive pulmonary disease (COPD) and resting or exercise-induced
107 t airway inflammation in chronic obstructive pulmonary disease (COPD) are incompletely understood.
111 ies comparing asthma and chronic obstructive pulmonary disease (COPD) based on thoracic quantitative
112 ilation in patients with chronic obstructive pulmonary disease (COPD) by using free-breathing dynamic
113 ce for the management of chronic obstructive pulmonary disease (COPD) comes from closely monitored ef
116 1 cells in patients with chronic obstructive pulmonary disease (COPD) correlated with disease severit
117 regions have effects on chronic obstructive pulmonary disease (COPD) development, while long noncodi
119 hils are associated with chronic obstructive pulmonary disease (COPD) exacerbations among individuals
120 acterial pathogen during chronic obstructive pulmonary disease (COPD) exacerbations and is a plausibl
121 ve ventilation (NIV) for chronic obstructive pulmonary disease (COPD) exacerbations, helium/oxygen (h
122 l industry, and academic chronic obstructive pulmonary disease (COPD) experts with advisors from the
123 RATIONALE: Patients with chronic obstructive pulmonary disease (COPD) frequently have albuminuria (in
125 atory conditions such as chronic obstructive pulmonary disease (COPD) has not been investigated.
127 s in blood and sputum in chronic obstructive pulmonary disease (COPD) have been associated with incre
128 People with advanced chronic obstructive pulmonary disease (COPD) have distressing physical and p
129 havior and lung function/chronic obstructive pulmonary disease (COPD) have not been systematically ex
130 es to infect healthy and chronic obstructive pulmonary disease (COPD) human ciliated respiratory epit
131 deaths among people with chronic obstructive pulmonary disease (COPD) in England and Scotland 2011-20
132 susceptibility gene for chronic obstructive pulmonary disease (COPD) in genome-wide association stud
133 merging as biomarkers of chronic obstructive pulmonary disease (COPD) in individuals exposed to cigar
134 een childhood asthma and chronic obstructive pulmonary disease (COPD) in later life has been demonstr
135 ssociation of asthma and chronic obstructive pulmonary disease (COPD) in the same patient, which is d
137 : Acute exacerbations of chronic obstructive pulmonary disease (COPD) increase the risk of death and
152 ng to the development of chronic obstructive pulmonary disease (COPD) is crucial for developing new t
153 ONALE: The prevalence of chronic obstructive pulmonary disease (COPD) is increasing faster among wome
154 RATIONALE: The burden of chronic obstructive pulmonary disease (COPD) is increasing, yet there are li
160 ingly aging populations, chronic obstructive pulmonary disease (COPD) is the fourth leading cause of
161 ette smoke (CS) -induced chronic obstructive pulmonary disease (COPD) is the primary testing methodol
165 logic evidence suggested chronic obstructive pulmonary disease (COPD) might increase risk for abdomin
168 ; however, in asthma and chronic obstructive pulmonary disease (COPD) patients, this virus is a major
169 on risk in patients with chronic obstructive pulmonary disease (COPD) rely on a history of two or mor
170 Many individuals with chronic obstructive pulmonary disease (COPD) remain undiagnosed worldwide.
171 s for predicting risk of chronic obstructive pulmonary disease (COPD) require external validation in
172 rently, the diagnosis of chronic obstructive pulmonary disease (COPD) requires a ratio of forced expi
173 s after exacerbations of chronic obstructive pulmonary disease (COPD) requiring acute noninvasive ven
174 t the natural history of chronic obstructive pulmonary disease (COPD) that has developed from airway
175 atment for patients with chronic obstructive pulmonary disease (COPD) who have a high risk of exacerb
176 (n = 11) and those with chronic obstructive pulmonary disease (COPD) who were undergoing lung transp
178 l treatment decisions in chronic obstructive pulmonary disease (COPD), a personalized approach to car
179 8) of patients exhibited chronic obstructive pulmonary disease (COPD), although only 19 had been prev
181 aged 40 to 79 years have chronic obstructive pulmonary disease (COPD), and it is the third leading ca
182 diseases such as asthma, chronic obstructive pulmonary disease (COPD), and lung infections have criti
183 ovascular disease (CVD), chronic obstructive pulmonary disease (COPD), and lung-cancer mortality.
184 ARI), asthma, pneumonia, chronic obstructive pulmonary disease (COPD), and upper respiratory tract in
185 rway diseases, including chronic obstructive pulmonary disease (COPD), are associated with excessive
186 ing subphenotypes within chronic obstructive pulmonary disease (COPD), asthma, and other lung-related
187 ant in the management of chronic obstructive pulmonary disease (COPD), but can slightly increase the
188 airway in patients with chronic obstructive pulmonary disease (COPD), but their clinical and pathoph
189 atures of HIV-associated chronic obstructive pulmonary disease (COPD), but these changes have not bee
192 lipidemia, hypertension, chronic obstructive pulmonary disease (COPD), ulcer history, use of proton p
193 lying CONDOR to eQTLs in chronic obstructive pulmonary disease (COPD), we found the global network "h
194 iduals and in those with chronic obstructive pulmonary disease (COPD), whereas shorter-term exposure
195 r-old man suffering from chronic obstructive pulmonary disease (COPD), who presented with non-massive
222 that was consistent with chronic obstructive pulmonary disease (COPD); these participants were more l
224 er (LC; P=4.0 x 10(-4)), chronic obstructive pulmonary disease (COPD; P=9.3 x 10(-4)), peripheral art
225 eases such as asthma and chronic obstructive pulmonary diseases (COPD) affect more than one-half bill
226 (Genetic Epidemiology of Chronic Obstructive Pulmonary Disease [COPD]; non-Hispanic white and African
227 Genetic Epidemiology of Chronic Obstructive Pulmonary Disease (COPDGene) study to examine the role o
228 ary parameters to detect chronic obstructive pulmonary diseases (COPDs) such as asthma, bronchitis, o
229 dy mass index, diabetes, chronic obstructive pulmonary disease, coronary artery disease, peripheral a
231 elated acute lung injury), for assessment of pulmonary disease course and therapy, and in pulmonary t
232 ncluding specialists in infectious diseases, pulmonary diseases, critical care, and surgeons, anesthe
234 disease, heart failure, chronic obstructive pulmonary disease, diabetes mellitus, nitrate use, and e
235 n from two unrelated kindreds died of severe pulmonary disease during infancy following viral pneumon
236 cation, body mass index, chronic obstructive pulmonary disease, emphysema, personal history of cancer
237 eases such as asthma and chronic obstructive pulmonary disease, estimating physiologic impairment, an
239 utcomes of patients with chronic obstructive pulmonary disease exacerbation treated with noninvasive
243 armacologic treatment of chronic obstructive pulmonary disease has consistent beneficial and plausibl
244 c association studies in chronic obstructive pulmonary disease have primarily tested for association
246 in children and adults, chronic obstructive pulmonary disease, hypertension, diabetes, obesity, perc
249 mycobacteria (NTM) are an important cause of pulmonary disease in patients with cystic fibrosis (CF).
251 ed our understanding of the heterogeneity of pulmonary disease in smokers, they have not yet translat
252 ases, such as asthma and chronic obstructive pulmonary disease, include not only diagnostics (especia
254 criptional repertoire of chronic obstructive pulmonary disease, IPF, or normal histology lungs using
259 cerebrovascular disease, chronic obstructive pulmonary disease, lung cancer, and lower respiratory in
260 abnormalities documented in a wide array of pulmonary diseases may profoundly affect symptoms and pr
262 ofile but with increased chronic obstructive pulmonary disease, migraine, and affective disorders.
264 s to limit the impact of chronic obstructive pulmonary disease on everyday life of individuals and to
265 tic treatment and with no history of chronic pulmonary disease or use of asthma medication in the pas
266 .46; 95% CI, 0.36-0.59), chronic obstructive pulmonary disease (OR, 0.62; 95% CI, 0.52-0.75), diabete
267 .12-1.39; P < .001), and chronic obstructive pulmonary disease (OR, 1.26; 95% CI, 1.09-1.45; P = .002
268 terstitial lung disease, chronic obstructive pulmonary disease, or pulmonary arterial hypertension.
269 R 1.71; asthma: OR 1.56; chronic obstructive pulmonary disease: OR 1.65; cancer: OR 1.23; weak/failin
270 , 30-day readmission for chronic obstructive pulmonary disease (p = 0.83), or hospital length of stay
271 (older age, female sex, chronic obstructive pulmonary disease; P<0.05 for all), periprocedural major
272 ve recently gained attention in the field of pulmonary diseases, particularly in asthma and chronic o
273 aired ejection fraction, chronic obstructive pulmonary disease, peripheral vascular disease, or renal
274 , rheumatoid arthritis, Alzheimer's disease, pulmonary disease, pre-term delivery of low birth weight
277 ls from individuals with chronic obstructive pulmonary disease recapitulated features of the disease
279 1beta responses occur in chronic obstructive pulmonary disease, respiratory infections, and neutrophi
280 ts with cystic fibrosis, chronic obstructive pulmonary disease, severe asthma, pre-existing pulmonary
283 y due to respiratory and chronic obstructive pulmonary disease specifically were positive but impreci
284 tro cell based biological assays for various pulmonary diseases such as acute respiratory distress sy
286 our understanding of the pathophysiology of pulmonary diseases that arise either as a consequence of
287 susceptibility gene for chronic obstructive pulmonary disease, the physiologic role of this protease
288 of 13,893 patients with chronic obstructive pulmonary disease treated with noninvasive ventilation.
289 49 subjects from three cohorts without known pulmonary disease, we observed that pneumotypeSPT was as
290 ronic kidney disease and chronic obstructive pulmonary disease were important risk factors for SCD/VA
292 erinflated patients with chronic obstructive pulmonary disease were randomized (1:1) to 7 (maximum 14
293 n mild-to-moderate stage chronic obstructive pulmonary disease where the rate of FEV1 decline is the
294 bowel disease) and lung (chronic obstructive pulmonary disease), where they contribute to IFN-gamma-m
296 uded 7,892 patients with chronic obstructive pulmonary disease who enrolled between 1981 and 2006.
298 ty of Life Assessment in Chronic Obstructive Pulmonary Disease with Closed Triple Therapy) trial was
299 he TIMP3 gene should be screened in familial pulmonary diseases with bronchiectasis, associated with
300 perammonaemia occurs in hepatic, cardiac and pulmonary diseases with increased muscle concentration o
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