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1 tological injury such as ALI or neutrophilic capillaritis.
2  those conditions with and without pulmonary capillaritis.
3 rotizing arteritis and hemorrhagic pulmonary capillaritis.
4       An open lung biopsy revealed pulmonary capillaritis.
5 erulitis, 6.1% vs. 32%, P=0.003; peritubular capillaritis: 13% vs. 40%, P=0.0009).
6 s in the C4d-positive group had neutrophilic capillaritis (54% vs. 29%, P = .035), there was no signi
7     More commonly found in adults, pulmonary capillaritis, an immune-mediated form of diffuse alveola
8 ose MPO-ANCA IgG induced MPA with NCGN, lung capillaritis and arteritis, but no granulomatosis.
9 merulitis, but similar levels of peritubular capillaritis and C4d deposition.
10                  However, isolated pulmonary capillaritis and DAH is not described for patients witho
11                           Isolated pulmonary capillaritis and DAH without systemic disease occurs in
12                                    ANCA lung capillaritis and microabscesses began within one day and
13  pauci-immune NCGN in all mice and pulmonary capillaritis and splenic necrotizing arteritis in some.
14 re damage (thrombosis, acute tubular injury, capillaritis) and infiltration of many Syk leukocytes.
15 ous MPO-ANCA IgG induced GPA with NCGN, lung capillaritis, arteritis and granulomatosis.
16  EGPA with eosinophilic bronchiolitis, NCGN, capillaritis, arteritis, and granulomatosis.
17              Most cases of DAH are caused by capillaritis associated with systemic autoimmune disease
18 is and changes in GFR (P<0.001), peritubular capillaritis Banff score (P=0.002), and DSA mean fluores
19 gic features resembling human posttransplant capillaritis, characterized by neutrophilic infiltration
20 e presence of DSA-I or II is associated with capillaritis during AR.
21        EndMT markers were more specific than capillaritis for the diagnosis and prognosis of ABMR and
22 prevalent, with glomerulitis and peritubular capillaritis found in 60.0% and 47.6% of 1-year biopsies
23 atients with DAH and biopsy-proven pulmonary capillaritis from seven Denver hospitals.
24 e antibody-mediated rejection manifesting as capillaritis (g>/=1 and ptc>/=1) with detectable donor-s
25 ciated with current ABMR criteria, including capillaritis, glomerulitis, peritubular capillary C4d de
26 2 MVI >= 2 (Banff glomerulitis + peritubular capillaritis &gt;= 2) samples by 9-mo median incidence time
27 incidence of MVI (glomerulitis + peritubular capillaritis &gt;= 2) than patients with cPRA = 0 [35% (17/
28 n we characterize DAH and isolated pulmonary capillaritis in the absence of clinical, serologic, or h
29 cally "borderline." DSA+ was associated with capillaritis in the biopsy (glomerulitis, 6.1% vs. 32%,
30 afts support the concept that posttransplant capillaritis is a form of humoral rejection.
31                                              Capillaritis is associated with reduced graft survival.
32 sis of exclusion and children with pulmonary capillaritis may have negative serology, lung biopsy sho
33 tio (OR): 4.83 (1.47-15.87), p = 0.0095, and capillaritis, OR: 3.03 (1.10-8.36), p = 0.033.
34 ary syphilis, cutaneous lupus erythematosus, capillaritis, pityriasis versicolor, nummular eczema, an
35 onents glomerulitis (g), C4d, g+ peritubular capillaritis (ptc) and acute composite score, but showed
36                Recently, diffuse peritubular capillaritis (ptc) has been suggested to independently p
37             Glomerulitis (g) and peritubular capillaritis (ptc) scores were independently correlated
38 addition of glomerulitis (g) and peritubular capillaritis (ptc) scores) to assess long-term graft sur
39 e sum of Banff glomerulitis (g), peritubular capillaritis (ptc), arteritis (v) and C4d scores, with a
40 sholds (Banff glomerulitis [g] + peritubular capillaritis [ptc] score >= 2) without DSA has been incr
41                                  Peritubular capillaritis scores 1, 2, and 3 were present in 36%, 55%
42 , interstitial inflammation, and peritubular capillaritis scores were also significantly higher in mi
43 In a series of eight children with pulmonary capillaritis, serology for immune-mediated disorders was
44 ular AMR activity and histologic peritubular capillaritis than DSA-positive AMR.
45 y macrophages manifested as glomerulitis and capillaritis.Throughout the course of AMR, lytic and sub
46 ar hemorrhage (DAH) resulting from pulmonary capillaritis typically accompanies the systemic vasculit
47             Compared with no AR, C4d-AR with capillaritis was associated with reduced graft survival
48                                  Peritubular capillaritis was detected in 50% (76% mononuclear ptc).
49 survival (82.1% vs. 98.1%, P=0.004), whereas capillaritis was not (88.1% vs. 97.7% respectively, P=0.
50 cores including glomerulitis and peritubular capillaritis were lower on surveillance biopsies at 1, 5
51 cores including glomerulitis and peritubular capillaritis were lower on surveillance biopsies at 1, 5
52 ar injury scores (glomerulitis + peritubular capillaritis), were less in the TLN-treated animals.
53 res of antibody-mediated rejection including capillaritis with thrombosis, acute tubular injury, IgG
54 (28%) were diagnosed with isolated pulmonary capillaritis without clinical, serologic, or histologic