戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 is of other primary vasculitides, especially polyarteritis nodosa.
2 man in her 50s with a diagnosis of cutaneous polyarteritis nodosa.
3  patients who developed vasculitis mimicking polyarteritis nodosa and giant cell arteritis.
4 is, and those of medium-vessel arteritis are polyarteritis nodosa and Kawasaki disease.
5 henotype, as well as two young siblings with polyarteritis nodosa and one patient with small-vessel v
6 aphy findings led to a clinical diagnosis of polyarteritis nodosa, and immunosuppressive therapy was
7  Wegener's granulomatosis, Cogan's syndrome, polyarteritis nodosa, and systemic lupus erythematosus.
8 age, treating Kawasaki disease, and treating polyarteritis nodosa, but most reported feeling comforta
9 ith multiple cases of systemic and cutaneous polyarteritis nodosa, consistent with autosomal recessiv
10  implicated in the pathogenesis of cutaneous polyarteritis nodosa (cPAN) and early-onset vasculopathy
11                        A study of idiopathic polyarteritis nodosa demonstrates greater similarity to
12 ication criteria for Wegener granulomatosis, polyarteritis nodosa, giant-cell arteritis, and hypersen
13                                 The study of polyarteritis nodosa has additionally been affected by p
14  for vasculitis-related hospitalizations for polyarteritis nodosa, hypersensitivity vasculitis, Wegen
15                                              Polyarteritis nodosa is a form of necrotizing vasculitis
16                                              Polyarteritis nodosa is a systemic necrotizing vasculiti
17  cytoplasmic antibody-associated vasculitis, polyarteritis nodosa, Kawasaki disease, giant cell arter
18 pathy (recurrent fevers, livedo reticularis, polyarteritis nodosa, lacunar ischemic strokes, and intr
19 ystemic vasculitides with neuropathy include polyarteritis nodosa, microscopic polyangiitis (MPA), rh
20 y in patients with Wegener's granulomatosis, polyarteritis nodosa, microscopic polyangiitis, and Chur
21 1 mutations, whereas the three patients with polyarteritis nodosa or small-vessel vasculitis were hom
22 (relapsing polychondritis, Sweet's syndrome, polyarteritis nodosa, or giant-cell arteritis) or a hema
23 anulomatosis, polymyositis, dermatomyositis, polyarteritis nodosa, or scleroderma who had an emergent
24 noch-Schonlein purpura (HSP) and macroscopic polyarteritis nodosa (PAN) as early manifestations of Ig
25                                              Polyarteritis nodosa (PAN) has been used as a generic te
26                                              Polyarteritis nodosa (PAN) is a rare disease of childhoo
27                                              Polyarteritis nodosa (PAN) is regarded rightly as the gr
28 ment as a relatively common manifestation of polyarteritis nodosa (PAN), using the modern classificat
29  60% of Nppb-/- females developed mesenteric polyarteritis-nodosa (PAN)-like vasculitis in their life
30 's granulomatosis, inflammatory myopathy, or polyarteritis nodosa rather than rheumatoid arthritis, a
31 akayasu arteritis, giant cell arteritis, and polyarteritis nodosa) to atherosclerosis, display remark
32 extracellular adenosine deaminase, can cause polyarteritis nodosa vasculopathy with highly varied cli
33  of the first case of idiopathic vasculitis, polyarteritis nodosa, which even today is the basis of o