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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
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
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
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
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
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
43 ulonephritis, including 69 with evidence for microscopic polyangiitis, were evaluated for this study.
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