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1 t of interstitial fibrosis and bronchiolitis obliterans.
2 opathic pneumonia syndrome and bronchiolitis obliterans.
3 nt might be an option to treat bronchiolitis obliterans.
4  the condition is often called bronchiolitis obliterans.
5 ome the challenge presented by bronchiolitis obliterans.
6 angiographically involved in thromboangiitis obliterans.
7 irway obstruction arising from bronchiolitis obliterans.
8 rcome in long-term survival is bronchiolitis obliterans.
9 t were reported to have severe bronchiolitis obliterans.
10 manifesting as scleroderma and bronchiolitis obliterans.
11 cute rejection; none developed bronchiolitis obliterans.
12  dysfunction characteristic of bronchiolitis obliterans.
13 mmon causes of late death were bronchiolitis obliterans (35/61, 57%), infection (13/61, 21%), and pos
14 ival was 77% for patients with bronchiolitis obliterans, 37% for patients with IPS, and 36% for patie
15 s (obliterative bronchiolitis, bronchiolitis obliterans), acute bronchiolitis, diffuse panbronchiolit
16 d accuracy in diagnosing early bronchiolitis obliterans after lung transplantation.
17 ciated with the development of bronchiolitis obliterans after transplantation, we determined whether
18 y a role in the development of bronchiolitis obliterans after transplantation.
19              Asthma as well as bronchiolitis obliterans and chronic bronchitis are chronic lung disea
20 eatures distinguishing it from bronchiolitis obliterans and idiopathic pulmonary fibrosis.
21 stic fibrosis, post-transplant bronchiolitis obliterans and more recently chronic obstructive pulmona
22 ociations between diacetyl and bronchiolitis obliterans and other severe respiratory diseases observe
23 uent disease, earlier onset of bronchiolitis obliterans and shorter survival.
24 ht be helpful to better manage bronchiolitis obliterans and to detect and treat it earlier.
25 however, including infections, bronchiolitis obliterans, and complications of immunosuppression remai
26 atients with panbronchiolitis, bronchiolitis obliterans, and rejection after lung transplant.
27 c pneumonia syndrome (IPS) and bronchiolitis obliterans are now recognized as part of a spectrum of p
28  of patients with fibrosis and bronchiolitis obliterans, at each successive scheduled surveillance ti
29  and skin leads to progressive bronchiolitis obliterans (BO) and scleroderma, respectively, for which
30 Given the impact of T cells on bronchiolitis obliterans (BO) in lung transplantation, we used an esta
31                                Bronchiolitis obliterans (BO) is a detrimental late pulmonary complica
32                                Bronchiolitis obliterans (BO) is the pathologic manifestation of chron
33  of lung transplantation, with bronchiolitis obliterans (BO) representing the predominant pathologica
34            The pathogenesis of bronchiolitis obliterans (BO), a common and devastating obliterative d
35  graft survival, occurrence of bronchiolitis obliterans (BO), and episodes of rejection.
36 y obliteration, which leads to bronchiolitis obliterans (BO), which is pathognomonic for cGVHD of the
37 ymphocytic bronchitis (LB) and bronchiolitis obliterans (BO).
38  system cGVHD model that induces bronchiolar obliterans (BO).
39  viremia increases the risk of bronchiolitis obliterans (BOS) or death and retransplantation in the f
40 traluminal fibrotic lesions of bronchiolitis obliterans by day 28.
41 they probably had occupational bronchiolitis obliterans caused by the inhalation of volatile butter-f
42 on and with the development of bronchiolitis obliterans could not be confirmed in human lung allograf
43                                Bronchiolitis obliterans developed in 29% of patients with a BALT-posi
44 hat results in scleroderma and bronchiolitis obliterans, diagnostic features of cGVHD.
45 tion course was complicated by bronchiolitis obliterans from chronic rejection and by recent pulmonar
46 se; in contrast, patients with bronchiolitis obliterans from Stevens-Johnson syndrome often have prog
47   Patients with postinfectious bronchiolitis obliterans generally have chronic, nonprogressive diseas
48 ith histopathologically proved bronchiolitis obliterans (group A) and 21 with normal biopsy findings
49 Experimental models of IPS and bronchiolitis obliterans have proven useful to test strategies designe
50 ied to show histopathology for bronchiolitis obliterans in all allogeneic grafts.
51               The diagnosis of bronchiolitis obliterans in children can be made with confidence based
52 sis, treatment, and outcome of bronchiolitis obliterans in the nontransplant, pediatric population.
53 cidence of acute rejection and bronchiolitis obliterans in younger versus older children may reveal i
54                              Thromboangiitis obliterans is a nonatherosclerotic segmental inflammator
55 ifferent cGVHD model, in which bronchiolitis obliterans is a prominent manifestation, F4/80+ macropha
56                                Bronchiolitis obliterans is a rare form of chronic obstructive lung di
57 st disease (GVHD) and IPS, and bronchiolitis obliterans is pathognomonic of chronic GVHD.
58 udying rare diseases such as thromboangiitis obliterans is that there are no significant research dol
59                                Bronchiolitis obliterans is the leading cause of chronic graft failure
60 ary vascular disease (n = 44), bronchiolitis obliterans (n = 21), pulmonary alveolar proteinosis (n =
61 me (n=4), hemosiderosis (n=1), bronchiolitis obliterans (n=1), sarcoidosis (n=1), and bronchiectasis
62 monary vascular disease (n=6), bronchiolitis obliterans (n=2), bronchopulmonary dysplasia (n=1), graf
63 neumonia syndrome (IPS, n=19), bronchiolitis obliterans (n=22), and other uncommon syndromes (n=5).
64                                Bronchiolitis obliterans organizing pneumonia (BOOP) and acute respira
65         The peak prevalence of bronchiolitis obliterans organizing pneumonia (BOOP) and interstitial
66                                Bronchiolitis obliterans organizing pneumonia (BOOP) has been reported
67 se alveolar damage (DAD) in 2, bronchiolitis obliterans organizing pneumonia (BOOP) in 1, and usual i
68                                Bronchiolitis obliterans organizing pneumonia (BOOP) is a clinical syn
69                                Bronchiolitis obliterans organizing pneumonia (BOOP) is a term that wa
70 neumonia (AIP), bronchiolitis, bronchiolitis obliterans organizing pneumonia (BOOP), and others.
71 hin air spaces consistent with bronchiolitis obliterans organizing pneumonia (BOOP).
72 obliterans syndrome (BOS), and bronchiolitis obliterans organizing pneumonia (BOOP).
73 ory distress syndrome (n = 2), bronchiolitis obliterans organizing pneumonia (n = 2), pulmonary embol
74 is, oral herpetic lesions, and bronchiolitis obliterans organizing pneumonia after 2 episodes of bact
75                                Bronchiolitis obliterans organizing pneumonia and erythema nodosum are
76 e case of a lady who developed bronchiolitis obliterans organizing pneumonia and erythema nodosum sim
77 ganizing pneumonia (idiopathic bronchiolitis obliterans organizing pneumonia), and pulmonary Langerha
78 ic interstitial pneumonitis, bronchoalveolar obliterans organizing pneumonia, focal fibrosis, pulmona
79 pneumonia, and the seventh had bronchiolitis obliterans organizing pneumonia.
80          The pathomechanism of bronchiolitis obliterans remains unclear and it remains a fatal compli
81  within 3 months of developing bronchiolitis obliterans syndrome (8.3 [1.4-25.1] vs. 3.6 [0.6-17.1] p
82 T studies in six patients with bronchiolitis obliterans syndrome (age range, 2 months to 5 1/2 years)
83  In past years, a diagnosis of bronchiolitis obliterans syndrome (BOS) after allogeneic hematopoietic
84 are the standard treatment for bronchiolitis obliterans syndrome (BOS) after allogeneic hematopoietic
85                                Bronchiolitis obliterans syndrome (BOS) after lung transplantation (LT
86 orphisms on the development of bronchiolitis obliterans syndrome (BOS) after lung transplantation.
87 ng log-rank test, freedom from bronchiolitis obliterans syndrome (BOS) and graft survival were compar
88 nally recognized definition of bronchiolitis obliterans syndrome (BOS) and longer follow up of heart-
89 raft dysfunction manifested as bronchiolitis obliterans syndrome (BOS) and worse posttransplant survi
90                   Freedom from bronchiolitis obliterans syndrome (BOS) at three years was similar in
91                 Development of bronchiolitis obliterans syndrome (BOS) following lung transplantation
92 an system cGVHD and associated bronchiolitis obliterans syndrome (BOS) in a murine model, we hypothes
93 n on survival and the onset of bronchiolitis obliterans syndrome (BOS) in consecutive lung transplant
94 associated with development of bronchiolitis obliterans syndrome (BOS) in human lung allografts.
95 ansplantation fails to prevent bronchiolitis obliterans syndrome (BOS) in many patients, primarily a
96 ansplantation fails to prevent bronchiolitis obliterans syndrome (BOS) in many patients, primarily a
97                       The term bronchiolitis obliterans syndrome (BOS) is a clinical surrogate for th
98                                Bronchiolitis obliterans syndrome (BOS) is a condition of progressive
99             Early diagnosis of bronchiolitis obliterans syndrome (BOS) is critical in understanding p
100 ograft rejection manifested as bronchiolitis obliterans syndrome (BOS) is the leading cause of late d
101                                Bronchiolitis obliterans syndrome (BOS) is the major limitation to sur
102                                Bronchiolitis obliterans syndrome (BOS) is the major limitation to sur
103                                Bronchiolitis obliterans syndrome (BOS) is the major obstacle to long-
104                                Bronchiolitis obliterans syndrome (BOS) is the most common cause of mo
105                                Bronchiolitis obliterans syndrome (BOS) is the primary limiting factor
106 function (CLAD), presenting as bronchiolitis obliterans syndrome (BOS) or restrictive allograft syndr
107 elopment of chronic rejection, bronchiolitis obliterans syndrome (BOS) remain major limiting factors
108                                Bronchiolitis obliterans syndrome (BOS) remains the leading obstacle t
109                                Bronchiolitis obliterans syndrome (BOS) remains the main cause of graf
110 of the allograft airway during bronchiolitis obliterans syndrome (BOS) that occurs after lung transpl
111                                Bronchiolitis obliterans syndrome (BOS), a condition of irreversible s
112 ung transplant recipients with bronchiolitis obliterans syndrome (BOS), a condition previously regard
113 nfectious complications and by bronchiolitis obliterans syndrome (BOS), a form of chronic rejection l
114                                Bronchiolitis obliterans syndrome (BOS), a process of fibro-obliterati
115 thic pneumonia syndrome (IPS), bronchiolitis obliterans syndrome (BOS), and bronchiolitis obliterans
116 ic rejection that manifests as bronchiolitis obliterans syndrome (BOS), but no biomarker can currentl
117 CXC chemokines associated with bronchiolitis obliterans syndrome (BOS), but the effect of pseudomonas
118 ransplantation, manifesting as bronchiolitis obliterans syndrome (BOS), has become the dominant chall
119 ve airflow obstruction, termed bronchiolitis obliterans syndrome (BOS), is the major cause of poor ou
120 raft rejection, represented by bronchiolitis obliterans syndrome (BOS), is the single most important
121 orders and risk for subsequent bronchiolitis obliterans syndrome (BOS), mortality and graft loss for
122                                Bronchiolitis obliterans syndrome (BOS), pathognomonic for chronic gra
123                                Bronchiolitis obliterans syndrome (BOS), the clinical correlate of chr
124                                Bronchiolitis obliterans syndrome (BOS), the major cause of death on l
125 literative lesion found during bronchiolitis obliterans syndrome (BOS), we hypothesized that the type
126 phy morphology, mortality, and bronchiolitis obliterans syndrome (BOS)-free survival were analyzed up
127 ften due to the development of bronchiolitis obliterans syndrome (BOS).
128  limited by the development of bronchiolitis obliterans syndrome (BOS).
129 fection) (NORMAL POST) or with bronchiolitis obliterans syndrome (BOS).
130 mary endpoint was freedom from bronchiolitis obliterans syndrome (BOS).
131 r lung transplantation (LT) is bronchiolitis obliterans syndrome (BOS).
132 ortant role in the etiology of bronchiolitis obliterans syndrome (BOS).
133 elated with the development of bronchiolitis obliterans syndrome (BOS).
134 ecline in lung function termed bronchiolitis obliterans syndrome (BOS).
135 y contribute to development of bronchiolitis obliterans syndrome (BOS).
136 ronic allograft failure termed bronchiolitis obliterans syndrome (BOS).
137 of chronic rejection, known as bronchiolitis obliterans syndrome (BOS).
138 ury would increase the risk of bronchiolitis obliterans syndrome (BOS).
139 an established risk factor for bronchiolitis obliterans syndrome (BOS).
140 ol analysis shows incidence of bronchiolitis obliterans syndrome (BOS): 1/43 in the Everolimus group
141 outcomes included freedom from bronchiolitis obliterans syndrome (fBOS) and rates of acute rejection.
142  in obliterative bronchiolitis/bronchiolitis obliterans syndrome (OB/BOS), which severely limits surv
143 09) and increased freedom from bronchiolitis obliterans syndrome (P = 0.03) was observed in the Celsi
144  nor a subsequent diagnosis of bronchiolitis obliterans syndrome (P=0.70).
145 r causes (currently defined as bronchiolitis obliterans syndrome [BOS]) is considered to reflect the
146 ts may develop an obstructive (bronchiolitis obliterans syndrome [BOS]) or a restrictive lung functio
147 iagnosis of chronic rejection (bronchiolitis obliterans syndrome [BOS]) was made in 191 patients (42.
148 Different clinical phenotypes (bronchiolitis obliterans syndrome [BOS]-neutrophilic BOS-restrictive a
149 nfants and young children with bronchiolitis obliterans syndrome after lung transplantation are more
150 f multiorgan system cGVHD with bronchiolitis obliterans syndrome and a minor MHC mismatch model of sc
151 investigate the development of bronchiolitis obliterans syndrome and graft loss after LTX in relation
152 graft rejection in the form of bronchiolitis obliterans syndrome and its histopathologic correlate, o
153 se current literature suggests bronchiolitis obliterans syndrome and restrictive allograft syndrome a
154 urrent diagnostic criteria for bronchiolitis obliterans syndrome and reviews the epidemiology, pathog
155 plant recipients who developed bronchiolitis obliterans syndrome and were compared to stable controls
156  Emphysema, female gender, and bronchiolitis obliterans syndrome are risk factors for severe HGG.
157 ted that the increased risk of bronchiolitis obliterans syndrome associated with primary graft dysfun
158 ints were overall survival and bronchiolitis obliterans syndrome at 2 years.
159  predisposed to development of bronchiolitis obliterans syndrome but particularly to restrictive allo
160 rvival and an earlier onset of bronchiolitis obliterans syndrome compared with patients in the transp
161 tial new therapeutic target in bronchiolitis obliterans syndrome deserving of a randomized placebo co
162                 This resembles bronchiolitis obliterans syndrome developed following human lung trans
163 r clinical variables including bronchiolitis obliterans syndrome did not change this relationship.
164 sease affects the lung tissue, bronchiolitis obliterans syndrome ensues.
165 wever, toward reduced onset of bronchiolitis obliterans syndrome grade 2 or 3 was observed in TLR4 he
166  multivariable model including bronchiolitis obliterans syndrome grade and baseline FEV1% predicted (
167                  Patients with bronchiolitis obliterans syndrome had a higher risk of severe HGG than
168                                Bronchiolitis obliterans syndrome has been associated with increased m
169 roblasts in the development of bronchiolitis obliterans syndrome has not been evaluated.
170 ansplantation, and potentially bronchiolitis obliterans syndrome in lung transplant recipients, with
171 de therapy in the treatment of bronchiolitis obliterans syndrome in lung transplant recipients.
172 gress of medical management of bronchiolitis obliterans syndrome include difficulties and delays in d
173 ated with an increased risk of bronchiolitis obliterans syndrome independent of acute rejection, lymp
174                                Bronchiolitis obliterans syndrome is a fibrotic occlusion of distal ai
175                                Bronchiolitis obliterans syndrome is a major problem for medium-to-lon
176                                Bronchiolitis obliterans syndrome is caused by a fibroproliferative pr
177                                Bronchiolitis obliterans syndrome is characterized by fibrotic obliter
178                                Bronchiolitis obliterans syndrome is the leading cause of chronic lung
179 ed into three groups: no CLAD (bronchiolitis obliterans syndrome level 0 [BOS 0]), early CLAD (BOS 0p
180       Recent data suggest that bronchiolitis obliterans syndrome may affect up to 6% of HSCT recipien
181 graft dysfunction manifests as bronchiolitis obliterans syndrome or the recently described restrictiv
182  factor for the development of bronchiolitis obliterans syndrome or worse overall survival.
183                                Bronchiolitis obliterans syndrome remains the leading cause of morbidi
184 spiratory viral infection is a bronchiolitis obliterans syndrome risk factor and virus-dependent inju
185 he remaining four patients had bronchiolitis obliterans syndrome scores of 0 compared with 5 of 13 co
186 ignificantly increased risk of bronchiolitis obliterans syndrome stage 1 (grade 1: relative risk [RR]
187 n, lymphocytic bronchitis, and bronchiolitis obliterans syndrome stage 1, using univariable and multi
188                   Freedom from bronchiolitis obliterans syndrome was lower, and mortality was higher
189 n of bronchial dilatation with bronchiolitis obliterans syndrome was significant (P = .02).
190 atients with clinically proved bronchiolitis obliterans syndrome were mosaic perfusion in five (83%)
191         Small airway fibrosis (bronchiolitis obliterans syndrome) is the primary obstacle to long-ter
192 onic lung allograft rejection (bronchiolitis obliterans syndrome) remains to be elucidated.
193  patients (5%) who experienced bronchiolitis obliterans syndrome, 15 (6%) were in the azithromycin gr
194 al RNA (HCV RNA), freedom from bronchiolitis obliterans syndrome, acute rejection, and survival.
195  factor for the development of bronchiolitis obliterans syndrome, an important cause of late mortalit
196 , renal dysfunction, diabetes, bronchiolitis obliterans syndrome, and malignancy.
197  months, bacterial infections, bronchiolitis obliterans syndrome, and survival.
198 five patients with progressive bronchiolitis obliterans syndrome, anti-TNFalpha treatment improved fo
199  limited by chronic rejection (bronchiolitis obliterans syndrome, BOS).
200 rophylaxis reduces the risk of bronchiolitis obliterans syndrome, but a controlled trial is awaited.
201 ion is a major risk factor for bronchiolitis obliterans syndrome, but noninvasive biomarkers have not
202 graft dysfunction, manifest by bronchiolitis obliterans syndrome, is frequent and limits long-term su
203 ses and in the pathogenesis of bronchiolitis obliterans syndrome, the predominant manifestation of ch
204 licated in the pathogenesis of bronchiolitis obliterans syndrome, which is considered to represent ch
205 g lung transplant recipients, "bronchiolitis obliterans syndrome," a disorder with clinical and histo
206 ality, follow-up survival, and bronchiolitis obliterans syndrome-free survival.
207 ate the in vivo development of bronchiolitis obliterans syndrome-like lesions and reveal its sensitiv
208 iopathic pneumonia syndrome or bronchiolitis obliterans syndrome.
209 g allograft rejection known as bronchiolitis obliterans syndrome.
210 tudy subjects remain free from bronchiolitis obliterans syndrome.
211 f primary graft dysfunction on bronchiolitis obliterans syndrome.
212  factor for the development of bronchiolitis obliterans syndrome.
213 served in the overall onset of bronchiolitis obliterans syndrome.
214  limited by the development of bronchiolitis obliterans syndrome.
215 lung function in patients with bronchiolitis obliterans syndrome.
216  factor for the development of bronchiolitis obliterans syndrome.
217 n linked to the development of bronchiolitis obliterans syndrome.
218 te rejection (AR) or developed bronchiolitis obliterans syndrome.
219 n increased risk of developing bronchiolitis obliterans syndrome.
220 idence of post-lung transplant bronchiolitis obliterans syndrome.
221 l to mesenchymal transition in bronchiolitis obliterans syndrome.
222  lung transplantation (LTX) is bronchiolitis obliterans syndrome.
223 patients prior to diagnosis of bronchiolitis obliterans syndrome.
224  acute cellular rejection, and bronchiolitis obliterans syndrome; however, the significance of circul
225  injury via TGF-beta in murine bronchiolitis obliterans; that TGF-beta and the C' cascade present sig
226 rease the chance of developing bronchiolitis obliterans; therefore, many centers perform surveillance
227  overall rate of occurrence of bronchiolitis obliterans was 46% (80/175) and the overall incidence of
228 onic illness in which meningeal endarteritis obliterans was consistently observed.
229 factors for the development of bronchiolitis obliterans were age older than 3 years, more than two ep
230 associated lymphoid tissue and bronchiolitis obliterans were unique for the immunizing virus, LCMV.
231 onsclerodermatous disease with bronchiolitis obliterans where cGVHD is dependent on antibody and germ
232 he major late complication was bronchiolitis obliterans, which occurred in 27% of patients and played
233                                Bronchiolitis obliterans with organizing pneumonia (BOOP) was the most
234 athy and pulmonary findings of bronchiolitis obliterans with organizing pneumonia (BOOP).

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