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

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