ライフサイエンスコーパス: polyarteritis

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1 implicated in the pathogenesis of cutaneous polyarteritis nodosa (cPAN) and early-onset vasculopathy

2 noch-Schonlein purpura (HSP) and macroscopic polyarteritis nodosa (PAN) as early manifestations of Ig

3 Polyarteritis nodosa (PAN) has been used as a generic te

4 Polyarteritis nodosa (PAN) is a rare disease of childhoo

5 Polyarteritis nodosa (PAN) is regarded rightly as the gr

6 ment as a relatively common manifestation of polyarteritis nodosa (PAN), using the modern classificat

7 henotype, as well as two young siblings with polyarteritis nodosa and one patient with small-vessel v

8 A study of idiopathic polyarteritis nodosa demonstrates greater similarity to

9 The study of polyarteritis nodosa has additionally been affected by p

10 Polyarteritis nodosa is a form of necrotizing vasculitis

11 Polyarteritis nodosa is a systemic necrotizing vasculiti

12 1 mutations, whereas the three patients with polyarteritis nodosa or small-vessel vasculitis were hom

13 's granulomatosis, inflammatory myopathy, or polyarteritis nodosa rather than rheumatoid arthritis, a

14 extracellular adenosine deaminase, can cause polyarteritis nodosa vasculopathy with highly varied cli

15 akayasu arteritis, giant cell arteritis, and polyarteritis nodosa) to atherosclerosis, display remark

16 aphy findings led to a clinical diagnosis of polyarteritis nodosa, and immunosuppressive therapy was

17 Wegener's granulomatosis, Cogan's syndrome, polyarteritis nodosa, and systemic lupus erythematosus.

18 age, treating Kawasaki disease, and treating polyarteritis nodosa, but most reported feeling comforta

19 ith multiple cases of systemic and cutaneous polyarteritis nodosa, consistent with autosomal recessiv

20 ication criteria for Wegener granulomatosis, polyarteritis nodosa, giant-cell arteritis, and hypersen

21 for vasculitis-related hospitalizations for polyarteritis nodosa, hypersensitivity vasculitis, Wegen

22 pathy (recurrent fevers, livedo reticularis, polyarteritis nodosa, lacunar ischemic strokes, and intr

23 ystemic vasculitides with neuropathy include polyarteritis nodosa, microscopic polyangiitis (MPA), rh

24 y in patients with Wegener's granulomatosis, polyarteritis nodosa, microscopic polyangiitis, and Chur

25 anulomatosis, polymyositis, dermatomyositis, polyarteritis nodosa, or scleroderma who had an emergent

26 of the first case of idiopathic vasculitis, polyarteritis nodosa, which even today is the basis of o

27 is of other primary vasculitides, especially polyarteritis nodosa.

28 man in her 50s with a diagnosis of cutaneous polyarteritis nodosa.

29 60% of Nppb-/- females developed mesenteric polyarteritis-nodosa (PAN)-like vasculitis in their life

30 tosis, microscopic polyangiitis (microscopic polyarteritis), the Churg-Strauss syndrome, idiopathic p

31 itis disorders (necrotizing arteritis of the polyarteritis type, hypersensitivity vasculitis, systemi

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