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1 imary vasculitides, especially polyarteritis nodosa.
2  with a diagnosis of cutaneous polyarteritis nodosa.
3 were infiltrated into leaves of Scrophularia Nodosa, an iridoid-producing plant species.
4 developed vasculitis mimicking polyarteritis nodosa and giant cell arteritis.
5 of medium-vessel arteritis are polyarteritis nodosa and Kawasaki disease.
6 ell as two young siblings with polyarteritis nodosa and one patient with small-vessel vasculitis.
7 led to a clinical diagnosis of polyarteritis nodosa, and immunosuppressive therapy was initiated.
8 nulomatosis, Cogan's syndrome, polyarteritis nodosa, and systemic lupus erythematosus.
9 Kawasaki disease, and treating polyarteritis nodosa, but most reported feeling comfortable treating c
10 ases of systemic and cutaneous polyarteritis nodosa, consistent with autosomal recessive inheritance.
11  the pathogenesis of cutaneous polyarteritis nodosa (cPAN) and early-onset vasculopathy.
12          A study of idiopathic polyarteritis nodosa demonstrates greater similarity to microscopic po
13 munodeficiency, liver disease, trichorrhexis nodosa, facial dysmorphism, hypopigmentation, and cardia
14 ia for Wegener granulomatosis, polyarteritis nodosa, giant-cell arteritis, and hypersensitivity vascu
15                   The study of polyarteritis nodosa has additionally been affected by proposed change
16 s-related hospitalizations for polyarteritis nodosa, hypersensitivity vasculitis, Wegener's granuloma
17                                Polyarteritis nodosa is a form of necrotizing vasculitis of small and
18                                Polyarteritis nodosa is a systemic necrotizing vasculitis with a patho
19 ntibody-associated vasculitis, polyarteritis nodosa, Kawasaki disease, giant cell arteritis, Takayasu
20 nt fevers, livedo reticularis, polyarteritis nodosa, lacunar ischemic strokes, and intracranial hemor
21 itides with neuropathy include polyarteritis nodosa, microscopic polyangiitis (MPA), rheumatoid vascu
22 with Wegener's granulomatosis, polyarteritis nodosa, microscopic polyangiitis, and Churg-Strauss synd
23 hereas the three patients with polyarteritis nodosa or small-vessel vasculitis were homozygous for th
24 ychondritis, Sweet's syndrome, polyarteritis nodosa, or giant-cell arteritis) or a hematologic condit
25  abnormalities (trichoschisis, trichorrhexis nodosa, or ribbon/twist).
26 polymyositis, dermatomyositis, polyarteritis nodosa, or scleroderma who had an emergent or urgent hos
27  purpura (HSP) and macroscopic polyarteritis nodosa (PAN) as early manifestations of IgA kappa multip
28                                Polyarteritis nodosa (PAN) has been used as a generic term for systemi
29                                Polyarteritis nodosa (PAN) is a rare disease of childhood.
30                                Polyarteritis nodosa (PAN) is regarded rightly as the grandfather of t
31 tively common manifestation of polyarteritis nodosa (PAN), using the modern classification of PAN pul
32 - females developed mesenteric polyarteritis-nodosa (PAN)-like vasculitis in their life span, some as
33 sis, inflammatory myopathy, or polyarteritis nodosa rather than rheumatoid arthritis, and were less l
34 tis, giant cell arteritis, and polyarteritis nodosa) to atherosclerosis, display remarkable target ti
35  analyses of an epiphytic orchid, Brassavola nodosa, to test for genetic discontinuity and to explore
36 adenosine deaminase, can cause polyarteritis nodosa vasculopathy with highly varied clinical expressi
37 case of idiopathic vasculitis, polyarteritis nodosa, which even today is the basis of our understandi