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1 ses can induce injury in MPO-ANCA-associated microscopic polyangiitis.
2 merly known as Wegener's granulomatosis) and microscopic polyangiitis.
3 ents with either Wegener's granulomatosis or microscopic polyangiitis.
4 d make this condition a separate entity from microscopic polyangiitis.
5  of vasculitis as Wegener granulomatosis and microscopic polyangiitis.
6 matosis with polyangiitis, but are absent in microscopic polyangiitis.
7 d patients with diagnosed Wegener disease or microscopic polyangiitis.
8 groups (47 Wegener's granulomatosis [WG], 12 microscopic polyangiitis, 16 Churg-Strauss syndrome [CSS
9 mely granulomatosis with polyangiitis (GPA), microscopic polyangiitis and eosinophilic GPA (EGPA), ar
10 l cytoplasmic autoantibody (ANCA)-associated microscopic polyangiitis and glomerulonephritis (excludi
11 nd treatment resistance in 107 patients with microscopic polyangiitis and necrotizing and crescentic
12 nd systemic small vessel vasculitis, such as microscopic polyangiitis and Wegener granulomatosis.
13 wly diagnosed AAV (Wegener granulomatosis or microscopic polyangiitis) and were aged 18 to 75 years a
14 th granulomatosis with polyangiitis, 23 with microscopic polyangiitis, and 5 with renal-limited ANCA-
15 ener's granulomatosis, polyarteritis nodosa, microscopic polyangiitis, and Churg-Strauss syndrome.
16 leukaemia, granulomatosis with polyangiitis, microscopic polyangiitis, and pemphigus vulagris.
17 seases, granulomatosis with polyangiitis and microscopic polyangiitis, and remains among the most dev
18         Granulomatosis with polyangiitis and microscopic polyangiitis are characterised by a necrotis
19  of children with Wegener granulomatosis and microscopic polyangiitis are derived by extrapolating fr
20                                       Severe microscopic polyangiitis can result in acute respiratory
21 e histological features of kidney disease in microscopic polyangiitis have been associated with clini
22 is nodosa demonstrates greater similarity to microscopic polyangiitis in relapse rate than previously
23                                              Microscopic polyangiitis is a subgroup of primary system
24                                              Microscopic polyangiitis is an autoimmune small-vessel v
25                                              Microscopic polyangiitis is defined within the context o
26 ation and management of renal involvement in microscopic polyangiitis is discussed, with emphasis on
27  granulomatosis, Churg-Strauss syndrome, and microscopic polyangiitis, is impeded by the small number
28 itis that includes Wegener's granulomatosis, microscopic polyangiitis (microscopic polyarteritis), th
29 ises granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA) and eosinophilic granulom
30 ses: granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA) and eosinophilic granulom
31                         The main phenotypes, microscopic polyangiitis (MPA) and granulomatosis with p
32      The distinction between classic PAN and microscopic polyangiitis (MPA) has not always been made.
33            Wegener's granulomatosis (WG) and microscopic polyangiitis (MPA) have been reported to be
34                                              Microscopic polyangiitis (MPA) may present with a syndro
35 with polyangiitis (GPA, formerly Wegener's), microscopic polyangiitis (MPA), and eosinophilic granulo
36 omatosis with polyangiitis (Wegener's; GPA), microscopic polyangiitis (MPA), and eosinophilic granulo
37 with granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), and eosinophilic granulo
38 matosis with polyangiitis (GPA) (Wegener's), microscopic polyangiitis (MPA), and kidney-limited disea
39 tis has diverse patterns of injury including microscopic polyangiitis (MPA), granulomatosis with poly
40 ith neuropathy include polyarteritis nodosa, microscopic polyangiitis (MPA), rheumatoid vasculitis, C
41 sculitides Wegener's granulomatosis (WG) and microscopic polyangiitis (MPA).
42 04 consecutive patients (64 with WG, 14 with microscopic polyangiitis [MPA], and 526 others) and 45 h
43                                              Microscopic polyangiitis, MPO-ANCA, higher serum creatin
44  years) received a KTX for ESRD secondary to microscopic polyangiitis (n=43) or Wegener's granulomato
45     It was concluded that most patients with microscopic polyangiitis or necrotizing and crescentic g
46 sis (granulomatosis with polyangiitis versus microscopic polyangiitis), or new diagnosis (versus rela
47  relapsing granulomatosis with polyangiitis, microscopic polyangiitis, or renal-limited ANCA-associat
48 emic lupus erythematosus (P = 2.7 x 10(-8)), microscopic polyangiitis (P = 2.9 x 10(-4)) and Wegener'
49 antineutrophil cytoplasmic antibody-positive microscopic polyangiitis, resulting in pulmonary hemorrh
50 to be more common at high latitudes, whereas microscopic polyangiitis shows the reverse pattern.
51 between granulomatosis with polyangiitis and microscopic polyangiitis that are associated with ANCA s
52 076) when controlling for age, ANCA pattern, microscopic polyangiitis versus glomerulonephritis alone
53 so that granulomatosis with polyangiitis and microscopic polyangiitis were genetically distinct.
54 ulonephritis, including 69 with evidence for microscopic polyangiitis, were evaluated for this study.