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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1963 11
1964 8
1966 3
1967 4
1968 6
1969 16
1970 8
1971 8
1972 8
1973 17
1974 10
1975 7
1976 10
1977 12
1978 3
1979 8
1980 11
1981 8
1982 10
1983 12
1984 5
1985 12
1986 7
1987 7
1988 14
1989 22
1990 24
1991 23
1992 20
1993 24
1994 41
1995 41
1996 25
1997 29
1998 20
1999 22
2000 25
2001 20
2002 18
2003 23
2004 24
2005 27
2006 20
2007 28
2008 25
2009 13
2010 19
2011 18
2012 21
2013 32
2014 20
2015 14
2016 23
2017 24
2018 28
2019 26
2020 20
2021 21
2022 27
2023 19
2024 6

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1,006 results

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Page 1
Polyarteritis nodosa revisited: a review of historical approaches, subphenotypes and a research agenda.
Karadag O, Jayne DJ. Karadag O, et al. Clin Exp Rheumatol. 2018 Mar-Apr;36 Suppl 111(2):135-142. Epub 2018 Feb 20. Clin Exp Rheumatol. 2018. PMID: 29465365 Free article. Review.
Polyarteritis nodosa (PAN) is a rare form of primary systemic vasculitis with heterogeneous presentations, treatments and disease course. ...
Polyarteritis nodosa (PAN) is a rare form of primary systemic vasculitis with heterogeneous presentations, treatments and dise …
Polyarteritis nodosa.
Bilginer Y, Ozen S. Bilginer Y, et al. Curr Opin Pediatr. 2022 Apr 1;34(2):229-233. doi: 10.1097/MOP.0000000000001106. Curr Opin Pediatr. 2022. PMID: 35081554 Review.
PURPOSE OF REVIEW: The aim is to review recent reports on childhood polyarteritis nodosa, including recent reports on treatment and outcome. ...We also aim to highlight differences of childhood polyarteritis nodosa with deficiency of ADA2 as well as ad …
PURPOSE OF REVIEW: The aim is to review recent reports on childhood polyarteritis nodosa, including recent reports on treatmen …
Diagnosis and classification of polyarteritis nodosa.
Hernández-Rodríguez J, Alba MA, Prieto-González S, Cid MC. Hernández-Rodríguez J, et al. J Autoimmun. 2014 Feb-Mar;48-49:84-9. doi: 10.1016/j.jaut.2014.01.029. Epub 2014 Jan 28. J Autoimmun. 2014. PMID: 24485157 Review.
Polyarteritis nodosa (PAN) is a systemic necrotizing vasculitis preferentially targeting medium-sized arteries and not associated with glomerulonephritis or small vessel involvement. ...
Polyarteritis nodosa (PAN) is a systemic necrotizing vasculitis preferentially targeting medium-sized arteries and not associa …
Medium- and Large-Vessel Vasculitis.
Saadoun D, Vautier M, Cacoub P. Saadoun D, et al. Circulation. 2021 Jan 19;143(3):267-282. doi: 10.1161/CIRCULATIONAHA.120.046657. Epub 2021 Jan 19. Circulation. 2021. PMID: 33464968 Review.
The most common causes of large-vessel vasculitis are giant cell arteritis and Takayasu arteritis, and those of medium-vessel arteritis are polyarteritis nodosa and Kawasaki disease. However, there is some overlap, and arteries of any size can potentially be involve …
The most common causes of large-vessel vasculitis are giant cell arteritis and Takayasu arteritis, and those of medium-vessel arteritis are …
Clinical Approach to Diagnosis and Therapy of Polyarteritis Nodosa.
Hočevar A, Tomšič M, Perdan Pirkmajer K. Hočevar A, et al. Curr Rheumatol Rep. 2021 Feb 10;23(3):14. doi: 10.1007/s11926-021-00983-2. Curr Rheumatol Rep. 2021. PMID: 33569653 Review.
PURPOSE OF THE REVIEW: Polyarteritis nodosa is a rare disease characterized by the necrotizing inflammation of medium-sized arteries. ...Microbiological and genetic investigations complement the diagnostic work-up. Idiopathic and hereditary variants of polyarteri …
PURPOSE OF THE REVIEW: Polyarteritis nodosa is a rare disease characterized by the necrotizing inflammation of medium-sized ar …
Pulmonary manifestations of large, medium, and variable vessel vasculitis.
Adams TN, Zhang D, Batra K, Fitzgerald JE. Adams TN, et al. Respir Med. 2018 Dec;145:182-191. doi: 10.1016/j.rmed.2018.11.003. Epub 2018 Nov 10. Respir Med. 2018. PMID: 30509707 Free article. Review.
The lung is commonly targeted in the more familiar ANCA-associated small vessel vasculitidies, but large and medium vessel vasculitides, including Takayasu arteritis, giant cell arteritis, polyarteritis nodosa, Behcet's disease, and necrotizing sarcoid granulomatosi …
The lung is commonly targeted in the more familiar ANCA-associated small vessel vasculitidies, but large and medium vessel vasculitides, inc …
Polyarteritis nodosa.
Forbess L, Bannykh S. Forbess L, et al. Rheum Dis Clin North Am. 2015;41(1):33-46, vii. doi: 10.1016/j.rdc.2014.09.005. Rheum Dis Clin North Am. 2015. PMID: 25399938 Review.
Polyarteritis nodosa (PAN) is a systemic disease, but variants are cutaneous PAN and single-organ disease. ...
Polyarteritis nodosa (PAN) is a systemic disease, but variants are cutaneous PAN and single-organ disease. ...
Granulomatous Vasculitis.
Sharma A, Dogra S, Sharma K. Sharma A, et al. Dermatol Clin. 2015 Jul;33(3):475-87. doi: 10.1016/j.det.2015.03.012. Dermatol Clin. 2015. PMID: 26143427 Review.
This group includes granulomatous vasculitides, namely, granulomatosis with polyangiitis (GPA), eosinophilic granulomatosis with polyangiitis (EGPA), and nongranulomatous vasculitis, namely, microscopic polyangiitis (MPA). Classic polyarteritis nodosa (PAN) is a gra …
This group includes granulomatous vasculitides, namely, granulomatosis with polyangiitis (GPA), eosinophilic granulomatosis with polyangiiti …
Polyarteritis nodosa.
Howard T, Ahmad K, Swanson JA, Misra S. Howard T, et al. Tech Vasc Interv Radiol. 2014 Dec;17(4):247-51. doi: 10.1053/j.tvir.2014.11.005. Epub 2014 Nov 13. Tech Vasc Interv Radiol. 2014. PMID: 25770638 Free PMC article. Review.
The first description of polyarteritis nodosa (PAN) was in 1852 by Karl Rokitansky, a pathologist at the University of Vienna. ...
The first description of polyarteritis nodosa (PAN) was in 1852 by Karl Rokitansky, a pathologist at the University of Vienna. …
EULAR/PRINTO/PRES criteria for Henoch-Schonlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part II: Final classification criteria.
Ozen S, Pistorio A, Iusan SM, Bakkaloglu A, Herlin T, Brik R, Buoncompagni A, Lazar C, Bilge I, Uziel Y, Rigante D, Cantarini L, Hilario MO, Silva CA, Alegria M, Norambuena X, Belot A, Berkun Y, Estrella AI, Olivieri AN, Alpigiani MG, Rumba I, Sztajnbok F, Tambic-Bukovac L, Breda L, Al-Mayouf S, Mihaylova D, Chasnyk V, Sengler C, Klein-Gitelman M, Djeddi D, Nuno L, Pruunsild C, Brunner J, Kondi A, Pagava K, Pederzoli S, Martini A, Ruperto N; Paediatric Rheumatology International Trials Organisation (PRINTO). Ozen S, et al. Ann Rheum Dis. 2010 May;69(5):798-806. doi: 10.1136/ard.2009.116657. Ann Rheum Dis. 2010. PMID: 20413568
OBJECTIVES: To validate the previously proposed classification criteria for Henoch-Schonlein purpura (HSP), childhood polyarteritis nodosa (c-PAN), c-Wegener granulomatosis (c-WG) and c-Takayasu arteritis (c-TA). ...
OBJECTIVES: To validate the previously proposed classification criteria for Henoch-Schonlein purpura (HSP), childhood polyarteritis …
1,006 results