Results 211 to 220 of about 16,344 (265)
Uncommon triple vessel spontaneous coronary artery dissection in the setting of polyarteritis nodosa: a case report. [PDF]
J Med Case RepLahmouch N +8 more
europepmc +1 more source
Ulcerative colitis: a diagnostic odyssey through cutaneous polyarteritis nodosa and granulomatous hepatitis. [PDF]
BMJ Case RepSoni J, Khosla P, Taneja V, Rao S.
europepmc +1 more source
Polyarteritis nodosa initially presenting as ocular motility impairment and diplopia with subsequent development of bilateral central retinal artery occlusion: A case report. [PDF]
Am J Ophthalmol Case RepNakagawa S, Akiyama S, Hino S, Ishii K.
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Radiology, 2023
Online supplemental material is available for this article.
Nanda Venkatanarasimha, Farah Irani
openaire +2 more sources
Online supplemental material is available for this article.
Nanda Venkatanarasimha, Farah Irani
openaire +2 more sources
Rheumatic Disease Clinics of North America, 2015
Polyarteritis nodosa (PAN) is a systemic disease, but variants are cutaneous PAN and single-organ disease. Histologic confirmation of vasculitis in medium-sized arteries is desirable, and biopsies should be obtained from the symptomatic and least invasive sites. Angiography can show multiple microaneurysms in the viscera.
Lindsy, Forbess, Serguei, Bannykh
+6 more sources
Polyarteritis nodosa (PAN) is a systemic disease, but variants are cutaneous PAN and single-organ disease. Histologic confirmation of vasculitis in medium-sized arteries is desirable, and biopsies should be obtained from the symptomatic and least invasive sites. Angiography can show multiple microaneurysms in the viscera.
Lindsy, Forbess, Serguei, Bannykh
+6 more sources
Current Opinion in Pediatrics, 2022
Purpose of review The aim is to review recent reports on childhood polyarteritis nodosa, including recent reports on treatment and outcome. Recently deficiency of adenosine deaminase-2 (ADA2), which may present as a polyarteritis nodosa-mimic, is becoming an important part of our practice.
Yelda, Bilginer, Seza, Ozen
openaire +2 more sources
Purpose of review The aim is to review recent reports on childhood polyarteritis nodosa, including recent reports on treatment and outcome. Recently deficiency of adenosine deaminase-2 (ADA2), which may present as a polyarteritis nodosa-mimic, is becoming an important part of our practice.
Yelda, Bilginer, Seza, Ozen
openaire +2 more sources
Comprehensive Therapy, 2007
Polyarteritis nodosa, as a diagnosis, has been progressively narrowed from a collection of ill-defined vasculitides to its current definition as a systemic transmural necrotizing vasculitis that usually affects medium-sized muscular arteries and sometimes small muscular arteries, commonly within the kidneys, gastrointestinal tract, skin, nerves, joints,
H David, Pettigrew +2 more
openaire +4 more sources
Polyarteritis nodosa, as a diagnosis, has been progressively narrowed from a collection of ill-defined vasculitides to its current definition as a systemic transmural necrotizing vasculitis that usually affects medium-sized muscular arteries and sometimes small muscular arteries, commonly within the kidneys, gastrointestinal tract, skin, nerves, joints,
H David, Pettigrew +2 more
openaire +4 more sources
Polyarteritis Nodosa and Cutaneous Polyarteritis Nodosa
SKINmed: Dermatology for the Clinician, 2003Cutaneous vasculitis can present with a variety of lesions and associated symptoms. It is important for the clinician to be able to recognize vasculitis lesions and know when to pursue further laboratory studies that will determine the extent of the disease process in a patient.
Courtney R, Herbert, Glenn G, Russo
openaire +2 more sources