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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
17 ciated with the development of bronchiolitis obliterans after transplantation, we determined whether
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
25 however, including infections, bronchiolitis obliterans, and complications of immunosuppression remai
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
33 of lung transplantation, with bronchiolitis obliterans (BO) representing the predominant pathologica
36 y obliteration, which leads to bronchiolitis obliterans (BO), which is pathognomonic for cGVHD of the
39 viremia increases the risk of bronchiolitis obliterans (BOS) or death and retransplantation in the f
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
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
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
55 ifferent cGVHD model, in which bronchiolitis obliterans is a prominent manifestation, F4/80+ macropha
58 udying rare diseases such as thromboangiitis obliterans is that there are no significant research dol
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).
67 se alveolar damage (DAD) in 2, bronchiolitis obliterans organizing pneumonia (BOOP) in 1, and usual i
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
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
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
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
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
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
100 ograft rejection manifested as bronchiolitis obliterans syndrome (BOS) is the leading cause of late d
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
110 of the allograft airway during bronchiolitis obliterans syndrome (BOS) that occurs after lung transpl
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
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
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
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
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
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
163 r clinical variables including bronchiolitis obliterans syndrome did not change this relationship.
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 (
170 ansplantation, and potentially bronchiolitis obliterans syndrome in lung transplant recipients, with
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
179 ed into three groups: no CLAD (bronchiolitis obliterans syndrome level 0 [BOS 0]), early CLAD (BOS 0p
181 graft dysfunction manifests as bronchiolitis obliterans syndrome or the recently described restrictiv
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
190 atients with clinically proved bronchiolitis obliterans syndrome were mosaic perfusion in five (83%)
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
198 five patients with progressive bronchiolitis obliterans syndrome, anti-TNFalpha treatment improved fo
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
207 ate the in vivo development of bronchiolitis obliterans syndrome-like lesions and reveal its sensitiv
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
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
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