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1 opsy revealed extrinsic allergic alveolitis (hypersensitivity pneumonitis).
2  and reduced survival in people with chronic hypersensitivity pneumonitis.
3 nts with sarcoidosis, beryllium disease, and hypersensitivity pneumonitis.
4 ffect on the TH1/TH17-mediated lung disease, hypersensitivity pneumonitis.
5 , chronic obstructive pulmonary disease, and hypersensitivity pneumonitis.
6 Saccharopolyspora rectivirgula in a model of hypersensitivity pneumonitis.
7 the pathogenesis of fibrosis in experimental hypersensitivity pneumonitis.
8 ntify occult antigen exposure known to cause hypersensitivity pneumonitis.
9 predominant source of IL-17A in experimental hypersensitivity pneumonitis.
10 specific interstitial pneumonia, and chronic hypersensitivity pneumonitis.
11 ffective way to control microbial Ag-induced hypersensitivity pneumonitis.
12  in this murine model of B. subtilis-induced hypersensitivity pneumonitis.
13 a domiciliana was the cause of the patient's hypersensitivity pneumonitis.
14 IFN-gamma is essential for the expression of hypersensitivity pneumonitis.
15  cleaning, she was diagnosed with summertype hypersensitivity pneumonitis.
16  idiopathic pulmonary fibrosis than fibrotic hypersensitivity pneumonitis (13 of 16 [81.2%] vs. 16 of
17 titial pneumonia with autoimmune features, 4 hypersensitivity pneumonitis, 5 connective tissue diseas
18 approximately one-third of all cases of ILD, hypersensitivity pneumonitis, accounting for 15% of ILD
19  with sarcoidosis, beryllium sensitivity, or hypersensitivity pneumonitis and healthy subjects were a
20 hoalveolar lavage fluid were consistent with hypersensitivity pneumonitis and positive for anti-Trich
21 inst S. rectivirgula in this murine model of hypersensitivity pneumonitis and pulmonary fibrosis.
22 sthma, Swyer-James syndrome, tracheomalacia, hypersensitivity pneumonitis and sarcoidosis.
23 opment of pulmonary fibrosis in experimental hypersensitivity pneumonitis and to determine the main i
24 ng biopsy that were consistent with subacute hypersensitivity pneumonitis (and IgG positive).
25  fibrosis (IPF), 4 patients with nonfibrotic hypersensitivity pneumonitis, and 36 healthy control sub
26 Ds, including idiopathic pulmonary fibrosis, hypersensitivity pneumonitis, and connective tissue dise
27 ases (pneumoconiosis, chemical pneumonitis), hypersensitivity pneumonitis, and electronic-cigarette-a
28  centre with recognised expertise in chronic hypersensitivity pneumonitis, and further research and s
29               The patient was diagnosed with hypersensitivity pneumonitis, and isocyanates (HDI) were
30 ria were subsequently diagnosed with chronic hypersensitivity pneumonitis, and most of these cases we
31 tive tissue disease-associated ILD, fibrotic hypersensitivity pneumonitis, and non-IPF idiopathic int
32                                Patients with hypersensitivity pneumonitis are at risk of developing p
33 posures, including avian antigens in chronic hypersensitivity pneumonitis, are not automatically excl
34  underlie the differential susceptibility to hypersensitivity pneumonitis between C57BL/6 and DBA/2 m
35 se findings suggested she had a bird-related hypersensitivity pneumonitis (BRHP).
36           These patients had no evidence for hypersensitivity pneumonitis, but 70% of cases had a per
37 nflammation in murine models of experimental hypersensitivity pneumonitis, but its role in the develo
38 opathic pulmonary fibrosis (IPF) and chronic hypersensitivity pneumonitis can be indistinguishable; t
39          This is the first described case of hypersensitivity pneumonitis cause by P. domiciliana.
40 play a regulatory role in the development of hypersensitivity pneumonitis caused by microbial Ags and
41  critical review of the current knowledge on hypersensitivity pneumonitis caused by the occupational
42      RATIONALE: Current diagnosis of chronic hypersensitivity pneumonitis (cHP) involves considering
43                           Rationale: Chronic hypersensitivity pneumonitis (CHP) is a condition that a
44 h-related quality of life of a large chronic hypersensitivity pneumonitis (CHP) patient sample.
45 ia (IIP), 46.5% of participants with chronic hypersensitivity pneumonitis (CHP), and 53.3% of partici
46        In the combined UCSF and UTSW chronic hypersensitivity pneumonitis cohort, we saw associations
47  with nosocomial infections and occupational hypersensitivity pneumonitis due to metalworking fluid (
48                          Rationale: Fibrotic hypersensitivity pneumonitis (FHP) is a debilitating int
49                          Rationale: Fibrotic hypersensitivity pneumonitis (fHP) is an interstitial lu
50 al interstitial pneumonia (UIP) and fibrotic hypersensitivity pneumonitis (fHP) patterns were assigne
51 s non-specific interstitial pneumonia, 16 as hypersensitivity pneumonitis, four as sarcoidosis, four
52 riod, and 16 of the 20 patients with chronic hypersensitivity pneumonitis had histopathological featu
53          In recent years, isocyanate-induced hypersensitivity pneumonitis has become rare, probably b
54       No clear effects of gender on rates of hypersensitivity pneumonitis have been shown.
55  type(s) that produce IL-17A in experimental hypersensitivity pneumonitis have not yet been identifie
56     Farmers lung disease is a common form of hypersensitivity pneumonitis (HP) and is characterized b
57                                              Hypersensitivity pneumonitis (HP) develops after inhalat
58                               Human cases of hypersensitivity pneumonitis (HP) have been reported amo
59                                              Hypersensitivity pneumonitis (HP) is a complex syndrome
60                                              Hypersensitivity pneumonitis (HP) is a complex syndrome
61                                              Hypersensitivity pneumonitis (HP) is a granulomatous, in
62                                              Hypersensitivity pneumonitis (HP) is a granulomatous, in
63                                              Hypersensitivity pneumonitis (HP) is a T(H)1 lymphocyte-
64                                              Hypersensitivity pneumonitis (HP) is an inflammatory lun
65                                              Hypersensitivity pneumonitis (HP) is an inflammatory lun
66                  Identifying early stages of hypersensitivity pneumonitis (HP) is hampered by variabl
67 ospectively compare in patients with chronic hypersensitivity pneumonitis (HP) the computed tomograph
68 ationale: Guidelines have defined a "typical hypersensitivity pneumonitis (HP)" imaging pattern for f
69                                              Hypersensitivity pneumonitis (HP), an inflammatory lung
70 d: This guideline addresses the diagnosis of hypersensitivity pneumonitis (HP).
71 hysicians (ACCP) imaging classifications for hypersensitivity pneumonitis (HP).
72 h those with IPF, whereas those with chronic hypersensitivity pneumonitis (HR, 0.67; 95% CI = 0.37, 1
73                             Final diagnosis: hypersensitivity pneumonitis in 47.3% (n = 513; exposure
74                                              Hypersensitivity pneumonitis in children is an underreco
75        We used a mouse model of experimental hypersensitivity pneumonitis in which IL-17A was inhibit
76                        Keywords: CT, Thorax, Hypersensitivity Pneumonitis, Interstitial Lung Disease
77                                              Hypersensitivity pneumonitis is an environmental lung di
78                                              Hypersensitivity pneumonitis is an immune-mediated inter
79                                              Hypersensitivity pneumonitis is an interstitial lung dis
80                                      Chronic hypersensitivity pneumonitis is characterized by pulmona
81 sciplinary team agreement for a diagnosis of hypersensitivity pneumonitis is low, highlighting an urg
82 NSIP; kappaw=0.42 [0.37-0.49]); and fair for hypersensitivity pneumonitis (kappaw=0.29 [0.24-0.40]).
83  [range, 23-86 years]), and 192 with chronic hypersensitivity pneumonitis (men, 76; women, 116; media
84  with idiopathic pulmonary fibrosis (n = 5), hypersensitivity pneumonitis (n = 5), and normal lung (n
85 elines had a subsequent diagnosis of chronic hypersensitivity pneumonitis: nine patients had positive
86 ); idiopathic pulmonary fibrosis (PAF, 26%); hypersensitivity pneumonitis (occupational burden, 19%);
87                                 Occupational hypersensitivity pneumonitis (OHP) is an immunologic lun
88 independent cohorts of patients with chronic hypersensitivity pneumonitis, one from the University of
89 urgical lung biopsy that was consistent with hypersensitivity pneumonitis; one was IgG positive plus
90 ding airway diseases; interstitial fibrosis; hypersensitivity pneumonitis; other noninfectious granul
91               Nine of 192 (4.7%) had chronic hypersensitivity pneumonitis (P < .001), and 27 of 244 (
92                   A CT appearance resembling hypersensitivity pneumonitis, reflecting the exquisitely
93 everal interstitial lung diseases, including hypersensitivity pneumonitis, respiratory bronchiolitis-
94            In most reported pediatric cases, hypersensitivity pneumonitis results from exposure to av
95 and assessed their associations with chronic hypersensitivity pneumonitis risk, survival, and clinica
96 sy showing a pattern consistent with chronic hypersensitivity pneumonitis); seven were IgG positive p
97 d son (patient 2) diagnosed with summer-type hypersensitivity pneumonitis (SHP).
98      She was diagnosed as having summer-type hypersensitivity pneumonitis (SHP).
99 nd reduced survival in patients with chronic hypersensitivity pneumonitis suggest shared pathobiology
100 n treatment, silicosis, sarcoidosis, chronic hypersensitivity pneumonitis, systemic sclerosis, and rh
101 or MUC5B rs35705950 in patients with chronic hypersensitivity pneumonitis than in healthy controls (2
102                          In a mouse model of hypersensitivity pneumonitis that progresses to lung fib
103      Previously, we have shown in a model of hypersensitivity pneumonitis that Th1-biased C57BL/6 mic
104                                              Hypersensitivity pneumonitis was induced in C57BL/6 wild
105                                              Hypersensitivity pneumonitis was the most common new-ons
106  asthma model, we found that the severity of hypersensitivity pneumonitis was unaffected by vancomyci
107     Using a well-established murine model of hypersensitivity pneumonitis, we repeatedly exposed C57B
108 athic nonspecific interstitial pneumonia and hypersensitivity pneumonitis, were reclassified as IPF.
109 lmonary fibrosis (IPF) or chronic (fibrotic) hypersensitivity pneumonitis, which suggests these disor

 
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