ライフサイエンスコーパス: nodosa

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1 imary vasculitides, especially polyarteritis nodosa.

2 with a diagnosis of cutaneous polyarteritis nodosa.

3 ell as two young siblings with polyarteritis nodosa and one patient with small-vessel vasculitis.

4 led to a clinical diagnosis of polyarteritis nodosa, and immunosuppressive therapy was initiated.

5 nulomatosis, Cogan's syndrome, polyarteritis nodosa, and systemic lupus erythematosus.

6 Kawasaki disease, and treating polyarteritis nodosa, but most reported feeling comfortable treating c

7 ases of systemic and cutaneous polyarteritis nodosa, consistent with autosomal recessive inheritance.

8 the pathogenesis of cutaneous polyarteritis nodosa (cPAN) and early-onset vasculopathy.

9 A study of idiopathic polyarteritis nodosa demonstrates greater similarity to microscopic po

10 munodeficiency, liver disease, trichorrhexis nodosa, facial dysmorphism, hypopigmentation, and cardia

11 ia for Wegener granulomatosis, polyarteritis nodosa, giant-cell arteritis, and hypersensitivity vascu

12 The study of polyarteritis nodosa has additionally been affected by proposed change

13 s-related hospitalizations for polyarteritis nodosa, hypersensitivity vasculitis, Wegener's granuloma

14 Polyarteritis nodosa is a form of necrotizing vasculitis of small and

15 Polyarteritis nodosa is a systemic necrotizing vasculitis with a patho

16 nt fevers, livedo reticularis, polyarteritis nodosa, lacunar ischemic strokes, and intracranial hemor

17 itides with neuropathy include polyarteritis nodosa, microscopic polyangiitis (MPA), rheumatoid vascu

18 with Wegener's granulomatosis, polyarteritis nodosa, microscopic polyangiitis, and Churg-Strauss synd

19 hereas the three patients with polyarteritis nodosa or small-vessel vasculitis were homozygous for th

20 abnormalities (trichoschisis, trichorrhexis nodosa, or ribbon/twist).

21 polymyositis, dermatomyositis, polyarteritis nodosa, or scleroderma who had an emergent or urgent hos

22 purpura (HSP) and macroscopic polyarteritis nodosa (PAN) as early manifestations of IgA kappa multip

23 Polyarteritis nodosa (PAN) has been used as a generic term for systemi

24 Polyarteritis nodosa (PAN) is a rare disease of childhood.

25 Polyarteritis nodosa (PAN) is regarded rightly as the grandfather of t

26 tively common manifestation of polyarteritis nodosa (PAN), using the modern classification of PAN pul

27 - females developed mesenteric polyarteritis-nodosa (PAN)-like vasculitis in their life span, some as

28 sis, inflammatory myopathy, or polyarteritis nodosa rather than rheumatoid arthritis, and were less l

29 tis, giant cell arteritis, and polyarteritis nodosa) to atherosclerosis, display remarkable target ti

30 adenosine deaminase, can cause polyarteritis nodosa vasculopathy with highly varied clinical expressi

31 case of idiopathic vasculitis, polyarteritis nodosa, which even today is the basis of our understandi

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