戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

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 ermined by computerized tomography (CT), and endobronchial abnormalities at bronchoscopy; (2) number,
2   Using a murine model, we demonstrated that endobronchial administration of antibodies (Abs) to majo
3 choalveolar space and change in FEV(1) after endobronchial allergen challenge (EBAC) in atopic asthma
4 e regional allergic reaction after segmental endobronchial allergen challenge.
5 ne challenge, inhaled allergen challenge and endobronchial allergen provocation through a bronchoscop
6 choline and inhaled allergen challenges, and endobronchial allergen provocations through a bronchosco
7 went two bronchoscopies with proximal airway endobronchial and distal alveolar tissue transbronchial
8 went two bronchoscopies with proximal airway endobronchial and distal alveolar tissue transbronchial
9                                              Endobronchial and transbronchial biopsies were performed
10         Similar results were obtained in the endobronchial and transbronchial biopsy specimens, which
11            Sections of concurrently obtained endobronchial and transbronchial/surgical biopsy tissue
12 transplantation, usually in association with endobronchial bacterial infection.
13 0 days after transplantation (n = 11) and/or endobronchial biopsies (n = 14) at 30 days for real-time
14 amined in blood, bronchoalveolar lavage, and endobronchial biopsies 48 hours after challenge.
15  the change in ASM transcriptomic profile in endobronchial biopsies after 14 days of oral glucocortic
16 expression of the protein phosphatase PP5 in endobronchial biopsies and ASM cells.
17  performed 6 h after each exposure to obtain endobronchial biopsies and bronchial wash (BW) cells.
18                                              Endobronchial biopsies and bronchoalveolar lavage fluid
19 protein-protein interactions are observed in endobronchial biopsies and fresh epithelial cells from a
20       We evaluated lymphocytic bronchitis on endobronchial biopsies as a risk factor for BOS and mort
21  compared the ASM transcriptomic profiles of endobronchial biopsies between glucocorticoid-free, atop
22 e chain reaction and immunohistochemistry in endobronchial biopsies from 13 subjects with mild and mo
23 hree different collagen staining methods, in endobronchial biopsies from 17 severe, nine moderate, an
24 y and quantitative real-time PCR analysis of endobronchial biopsies from 27 mild-to-moderate asthmati
25 tion of the bronchial epithelium observed in endobronchial biopsies from asthmatic subjects is a true
26 e that denudation of bronchial epithelium in endobronchial biopsies from asthmatic subjects with stab
27 eta2, and mucin expression were evaluated in endobronchial biopsies from asthmatics and normal subjec
28                We compared ASM cultured from endobronchial biopsies from subjects with and without as
29              Immunohistochemical staining of endobronchial biopsies identified epithelial localizatio
30 ion was also increased in the ASM bundles in endobronchial biopsies in severe asthmatics.
31 lls were determined in ultrathin sections of endobronchial biopsies obtained from 53 infants during c
32  gene expression profile of the ASM layer in endobronchial biopsies of patients with asthma is altere
33              Immunohistochemical staining of endobronchial biopsies revealed that KCa3.1 channels are
34              Immunohistochemical analyses of endobronchial biopsies showed a remarkable loss of caveo
35                                              Endobronchial biopsies were collected and graded during
36 an respiratory epithelial cells derived from endobronchial biopsies were cultured using a combination
37                                              Endobronchial biopsies were performed at the end of 12 w
38 dilation (DeltaR(rs) ) and bronchoscopy with endobronchial biopsies were performed.
39                                              Endobronchial biopsies were taken before and after 14 da
40 e, respectively), as well as mucosal tissue (endobronchial biopsies).
41 gene expression, quantitative morphometry of endobronchial biopsies, and levels of secreted protein.
42 r each exposure to obtain airway lavages and endobronchial biopsies.
43 vere asthma (N-SA; n = 8) were cultured from endobronchial biopsies.
44 pression in bronchoalveolar lavage cells and endobronchial biopsies.
45  challenge, and fiberoptic bronchoscopy with endobronchial biopsy (always right upper lobe second-gen
46           IL-33 expression was quantified in endobronchial biopsy (EB) specimens from children with S
47  induction, bronchoalveolar lavage (BAL) and endobronchial biopsy (EB).
48 e of macrophages/DC in lung allografts using endobronchial biopsy (EBB) and transbronchial biopsy (TB
49 ant diisocyanate-conjugated protein in human endobronchial biopsy samples, whereas albumin was the pr
50 ed and quantified by immunohistochemistry in endobronchial biopsy sections from smoking and non-smoki
51                       We sought to determine endobronchial biopsy specimen ASM area fraction in presc
52 hiolitis defined by pathological criteria on endobronchial biopsy specimens (in heart-lung/lung patie
53                                              Endobronchial biopsy specimens from allergen-challenged
54 lly differentiated bronchial epithelium from endobronchial biopsy specimens maintain inherent phenoty
55 Primary human fibroblasts were cultured from endobronchial biopsy specimens obtained from healthy or
56 nflammatory imbalances initially observed in endobronchial biopsy specimens obtained from patients wi
57 ultures of bronchial epithelium derived from endobronchial biopsy specimens of patients with differen
58 uman bronchial epithelial cells derived from endobronchial biopsy specimens of patients with mild and
59  and ASM mast cell values were quantified in endobronchial biopsy specimens previously obtained from
60 oduction, were assessed in paraffin-embedded endobronchial biopsy specimens to evaluate morphologic c
61 e density of FABP4-immunoreactive vessels in endobronchial biopsy specimens was significantly higher
62                                              Endobronchial biopsy specimens, epithelial brushings, an
63 inophils, followed by bronchoscopy, BAL, and endobronchial biopsy within 24 h.
64 nological sampling of blood, induced sputum, endobronchial biopsy, and bronchoalveolar lavage for flo
65 ical assessment and provided induced sputum, endobronchial biopsy, bronchoalveolar lavage, and blood
66  CS-dependent asthmatics were evaluated with endobronchial biopsy, pulmonary function, allergy testin
67 epithelial and endothelial cells obtained by endobronchial biopsy.
68 putum induction, bronchoalveolar lavage, and endobronchial biopsy.
69 nchoscopy, bronchoalveolar lavage (BAL), and endobronchial biopsy.
70                                           An endobronchial blocker was placed into the left main stem
71 ous positive airway pressure applied via the endobronchial blocker.
72 ion therapy were treated with palliative HDR endobronchial brachytherapy for symptoms due to relapse
73                                          HDR endobronchial brachytherapy is an effective method to re
74 had minimal symptomatic improvement with HDR endobronchial brachytherapy.
75 mptoms due to relapse or persistent tumor of endobronchial bronchogenic origin.
76 ere obtained by BAL, and BE were obtained by endobronchial brush biopsy from 15 grain handlers 6 h af
77 ed tomography-guided transthoracic biopsy or endobronchial brushing for undiagnosed nodules.
78 s (5 signatures), sputum (3 signatures), and endobronchial brushings (6 signatures).
79 utum (n = 83), nasal brushings (n = 41), and endobronchial brushings (n = 65) and biopsies (n = 47) (
80                                              Endobronchial brushings and biopsies were obtained and e
81                       DNA was extracted from endobronchial brushings and bronchoalveolar lavage fluid
82  in cultured bronchial epithelial cells from endobronchial brushings of both subject groups.
83  bronchoscopy, bronchoalveolar lavage (BAL), endobronchial brushings, and biopsy.
84  10(9) colony-forming units (CFU) GBS via an endobronchial catheter (n = 7).
85     Our findings suggest that treatment with endobronchial coils can improve quality of life for pati
86 rinflation treated for 12 months, the use of endobronchial coils compared with usual care resulted in
87 inary clinical trials have demonstrated that endobronchial coils compress emphysematous lung tissue a
88                                              Endobronchial coils might have a role in the treatment o
89                 While accepting that chronic endobronchial colonization with atypical mycobacteria ma
90 g the prostacyclin analogue iloprost reduces endobronchial dysplasia, a premalignant lung lesion.
91                                              Endobronchial endotoxin was followed by progressive alve
92 immediately extravascular by using primarily endobronchial forceps for caval fragments and snares for
93                                          The endobronchial forceps technique can be safely used to re
94                                          The endobronchial forceps technique was used to successfully
95 then removed through the sheath by using the endobronchial forceps.
96 al antibodies, variable bacterial clearance, endobronchial infection and microbial adaptation with PA
97 f the inflammatory response to P. aeruginosa endobronchial infection and that further investigation i
98                       Pseudomonas aeruginosa endobronchial infection causes significant morbidity and
99                                      Chronic endobronchial infection frequently caused by gram-negati
100  and systemic morbidity in mice with chronic endobronchial infection with P. aeruginosa embedded in a
101 ized by abnormal airways secretions, chronic endobronchial infection, and progressive airway obstruct
102 urine model of mucoid Pseudomonas aeruginosa endobronchial infection.
103 sociated with chronic Pseudomonas aeruginosa endobronchial infection.
104 using an animal model of chronic Pseudomonas endobronchial infection.
105 eudomonas aeruginosa strains causing chronic endobronchial infections in cystic fibrosis is their con
106 known as mucoidy, is associated with chronic endobronchial infections in cystic fibrosis.
107 roup was probably associated with accidental endobronchial intubation following tube movement.
108 opious secretions and in cases of accidental endobronchial intubation.
109 c intubation, aspiration, dental injury, and endobronchial intubation.
110 on Wegener's-related subglottic stenosis and endobronchial involvement, it has also become apparent t
111       Analysis of cytokine protein levels in endobronchial lavage (EBL) fluid demonstrated that only
112              The missed tumors manifested as endobronchial lesion (n = 10), solitary parenchymal nodu
113 = 5), pleural effusion (n = 4), and solitary endobronchial lesion (n = 2).
114 ruction promptly for patients with recurrent endobronchial lesions and may be considered as a boost f
115 owever, LC risk in patients with preinvasive endobronchial lesions is unclear.
116 hese results show that proteomic analysis of endobronchial lesions may facilitate the diagnosis of lu
117                                              Endobronchial location and lower lobe predominance were
118  we evaluated whether eosinophils within the endobronchial lumen can function in vivo as antigen-pres
119  Either bronchoscopy with transbronchial and endobronchial lung biopsies or endosonography (esophagea
120                                              Endobronchial lymphocytic bronchitis was more prevalent
121                           The association of endobronchial lymphocytic inflammation and BOS may have
122        The LLL was subsequently collapsed by endobronchial occlusion following 10 min of 100% O2.
123 e safely or effectively delivered, including endobronchial procedures using flexible or rigid broncho
124 ad severe alveolar inflammation and probable endobronchial sarcoidosis.
125 rs that control this homing pattern, we used endobronchial segmental allergen challenge in human atop
126 n CF, which typically remain confined to the endobronchial spaces, B. cenocepacia can traverse airway
127  10(9) plaque-forming units over 9 months by endobronchial spray to 7 pairs of individuals with CF.
128 m the lower airways of children with chronic endobronchial suppuration.
129                                              Endobronchial tamponade should only be used as a tempora
130         Preparation for other interventions (endobronchial tamponade, BAE, or surgery in eligible can
131  these polymorphisms were also compared with endobronchial tissue inflammatory cells and local IgE.
132 who underwent lung transplantation underwent endobronchial tissue oximetry of native and donor bronch
133                         Compared with native endobronchial tissues, donor tissue oxygen saturations (
134         Intubation with a 37-Fr double-lumen endobronchial tube and ventilation with two oscillatory
135 e a primary xenograft model of SCLC in which endobronchial tumor specimens obtained from chemo-naive
136                                              Endobronchial ulstrasound-guided core biopsies of the lu
137 ng biopsies or endosonography (esophageal or endobronchial ultrasonography) with aspiration of intrat
138 e lung cancer staging has evolved to include endobronchial ultrasonography-guided transbronchial need
139                                              Endobronchial ultrasonography-guided transbronchial need
140 ures and lymph nodes, is clearly imaged with endobronchial ultrasonography; (3) a greater short-axis
141 he diagnostic yield was 63.7% when no radial endobronchial ultrasound (r-EBUS) and no EMN were used,
142   Transbronchial needle aspiration guided by endobronchial ultrasound should be considered as the ini
143                                          The Endobronchial Ultrasound Skills and Tasks Assessment Too
144 mine whether the next step should be biopsy (endobronchial ultrasound-guided biopsy or mediastinoscop
145 N2 or N3 (prN2/3) malignant nodal disease on endobronchial ultrasound-guided transbronchial needle as
146                           We aimed to assess endobronchial ultrasound-guided transbronchial needle as
147 centres and randomly assigned them to either endobronchial ultrasound-guided transbronchial needle as
148 on on yield, complications, and tolerance of endobronchial ultrasound-guided transbronchial needle as
149                                    Real-time endobronchial ultrasound-guided transbronchial needle as
150                                  The role of endobronchial ultrasound-guided transbronchial needle as
151                                              Endobronchial ultrasound-guided transbronchial needle as
152                                              Endobronchial ultrasound-guided transbronchial needle as
153                                              Endobronchial ultrasound-guided transbronchial needle as
154 r randomized controlled trials of the Zephyr endobronchial valve (EBV) treatment have demonstrated be
155 ilot study of unilateral volume reduction by endobronchial valve insertion.
156 subjects with severe emphysema who underwent endobronchial valve LVR were analyzed retrospectively us
157                                              Endobronchial valve placement can improve lung volumes a
158                                              Endobronchial valve placement improves pulmonary functio
159       We compared the safety and efficacy of endobronchial-valve therapy in patients with heterogeneo
160 e of collateral ventilation to bronchoscopic endobronchial-valve treatment (EBV group) or to continue
161                                              Endobronchial-valve treatment for advanced heterogeneous
162                                              Endobronchial-valve treatment significantly improved pul
163 ause lobar segments were inaccessible to the endobronchial valves (3 patients).
164 ients, 220 were randomly assigned to receive endobronchial valves (EBV group) and 101 to receive stan
165                                              Endobronchial valves are designed to exclude the most af
166                For example, the placement of endobronchial valves can substitute for lung reduction s
167                         Previous trials with endobronchial valves have yielded modest group benefits
168              Unilateral lobar occlusion with endobronchial valves in patients with heterogeneous emph
169                                 Insertion of endobronchial valves in selected patients could have ben
170 ung-volume reduction with the use of one-way endobronchial valves is a potential treatment for patien
171                                              Endobronchial valves that allow air to escape from a pul
172       The most widely used BLVR devices are: endobronchial valves, foam sealant, metallic coils, airw
173 s were cultured from patient sputum (n = 3), endobronchial washings (n = 3), pleural fluid (n = 1), a

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top