Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1947 1
1951 1
1961 1
1963 1
1966 1
1967 2
1968 4
1969 5
1970 4
1971 6
1972 9
1973 5
1974 10
1975 4
1976 3
1977 7
1979 2
1980 6
1981 6
1982 7
1983 6
1984 3
1985 7
1986 11
1987 7
1988 6
1989 8
1990 10
1991 9
1992 7
1993 10
1994 10
1995 8
1996 7
1997 15
1998 11
1999 9
2000 8
2001 8
2002 6
2003 8
2004 6
2005 26
2006 17
2007 20
2008 17
2009 30
2010 28
2011 21
2012 27
2013 19
2014 28
2015 20
2016 13
2017 17
2018 34
2019 30
2020 26
2021 18
2022 24
2023 13
2024 6

Text availability

Article attribute

Article type

Publication date

Search Results

639 results

Results by year

Filters applied: . Clear all
Page 1
European consensus-based recommendations for diagnosis and treatment of immunoglobulin A vasculitis-the SHARE initiative.
Ozen S, Marks SD, Brogan P, Groot N, de Graeff N, Avcin T, Bader-Meunier B, Dolezalova P, Feldman BM, Kone-Paut I, Lahdenne P, McCann L, Pilkington C, Ravelli A, van Royen A, Uziel Y, Vastert B, Wulffraat N, Kamphuis S, Beresford MW. Ozen S, et al. Rheumatology (Oxford). 2019 Sep 1;58(9):1607-1616. doi: 10.1093/rheumatology/kez041. Rheumatology (Oxford). 2019. PMID: 30879080
OBJECTIVES: IgA vasculitis (IgAV, formerly known as Henoch-Schonlein purpura) is the most common cause of systemic vasculitis in childhood. ...Treatment recommendations included: the importance of appropriate analgesia and angiotensin-converting enzyme inhibitor use …
OBJECTIVES: IgA vasculitis (IgAV, formerly known as Henoch-Schonlein purpura) is the most common cause of systemic vasculitis …
2018 Update of the EULAR recommendations for the management of large vessel vasculitis.
Hellmich B, Agueda A, Monti S, Buttgereit F, de Boysson H, Brouwer E, Cassie R, Cid MC, Dasgupta B, Dejaco C, Hatemi G, Hollinger N, Mahr A, Mollan SP, Mukhtyar C, Ponte C, Salvarani C, Sivakumar R, Tian X, Tomasson G, Turesson C, Schmidt W, Villiger PM, Watts R, Young C, Luqmani RA. Hellmich B, et al. Ann Rheum Dis. 2020 Jan;79(1):19-30. doi: 10.1136/annrheumdis-2019-215672. Epub 2019 Jul 3. Ann Rheum Dis. 2020. PMID: 31270110
BACKGROUND: Since the publication of the European League Against Rheumatism (EULAR) recommendations for the management of large vessel vasculitis (LVV) in 2009, several relevant randomised clinical trials and cohort analyses have been published, which have the potential to …
BACKGROUND: Since the publication of the European League Against Rheumatism (EULAR) recommendations for the management of large vessel va …
Management of cutaneous vasculitis.
Micheletti RG, Pagnoux C. Micheletti RG, et al. Presse Med. 2020 Oct;49(3):104033. doi: 10.1016/j.lpm.2020.104033. Epub 2020 Jul 6. Presse Med. 2020. PMID: 32645416 Review.
Cutaneous vasculitis encompasses cutaneous components of systemic vasculitides, skin-limited variants of systemic vasculitides, such as IgA vasculitis or cutaneous polyarteritis nodosa, and single-organ cutaneous vasculitis, as individualized in …
Cutaneous vasculitis encompasses cutaneous components of systemic vasculitides, skin-limited variants of systemic vasculiti …
The diagnosis and management of temporal arteritis.
Ling ML, Yosar J, Lee BW, Shah SA, Jiang IW, Finniss A, Allende A, Francis IC. Ling ML, et al. Clin Exp Optom. 2020 Sep;103(5):572-582. doi: 10.1111/cxo.12975. Epub 2019 Oct 29. Clin Exp Optom. 2020. PMID: 31663193 Free article. Review.
Temporal arteritis (TA), or giant cell arteritis, is a systemic autoimmune vasculitis affecting patients over 50 years of age. It can cause rapid, irreversible bilateral vision loss in older adults and is therefore considered an ophthalmological emergency. ...
Temporal arteritis (TA), or giant cell arteritis, is a systemic autoimmune vasculitis affecting patients over 50 years of age. It can …
Polyclonal hypergammaglobulinaemia: assessment, clinical interpretation, and management.
Zhao EJ, Cheng CV, Mattman A, Chen LYC. Zhao EJ, et al. Lancet Haematol. 2021 May;8(5):e365-e375. doi: 10.1016/S2352-3026(21)00056-9. Lancet Haematol. 2021. PMID: 33894171 Review.
Causes of polyclonal hypergammaglobulinaemia can be divided into eight categories: liver disease, autoimmune disease and vasculitis, infection and inflammation, non-haematological malignancy, haematological disorders, IgG4-related disease, immunodeficiency syndromes, and i …
Causes of polyclonal hypergammaglobulinaemia can be divided into eight categories: liver disease, autoimmune disease and vasculitis, …
Cogan's Syndrome: Clinical Presentations and Update on Treatment.
Espinoza GM, Wheeler J, Temprano KK, Keller AP. Espinoza GM, et al. Curr Allergy Asthma Rep. 2020 Jun 16;20(9):46. doi: 10.1007/s11882-020-00945-1. Curr Allergy Asthma Rep. 2020. PMID: 32548646 Review.
PURPOSE OF REVIEW: Cogan's syndrome (CS) is a rare systemic vasculitis that can severely affect vision and hearing, which may also have significant systemic effects. ...
PURPOSE OF REVIEW: Cogan's syndrome (CS) is a rare systemic vasculitis that can severely affect vision and hearing, which may also ha …
Updates for the treatment of EGPA.
Raffray L, Guillevin L. Raffray L, et al. Presse Med. 2020 Oct;49(3):104036. doi: 10.1016/j.lpm.2020.104036. Epub 2020 Jul 8. Presse Med. 2020. PMID: 32652104 Review.
Eosinophilic granulomatosis with polyangiitis (EGPA, formerly Churg-Strauss syndrome) is the least frequent antineutrophil cytoplasm antibody (ANCA)-associated vasculitis (AAV). Major advances of our knowledge on its pathophysiology have revealed features of both AAV and e …
Eosinophilic granulomatosis with polyangiitis (EGPA, formerly Churg-Strauss syndrome) is the least frequent antineutrophil cytoplasm antibod …
Urticarial vasculitis: Clinical and laboratory findings with a particular emphasis on differential diagnosis.
Marzano AV, Maronese CA, Genovese G, Ferrucci S, Moltrasio C, Asero R, Cugno M. Marzano AV, et al. J Allergy Clin Immunol. 2022 Apr;149(4):1137-1149. doi: 10.1016/j.jaci.2022.02.007. J Allergy Clin Immunol. 2022. PMID: 35396080 Review.
Urticarial vasculitis (UV) is a rare cutaneous vasculitis of small vessels characterized by recurrent episodes of wheal-like lesions that tend to last more than 24 hours, healing with a residual ecchymotic postinflammatory hyperpigmentation. The histopathologic patt …
Urticarial vasculitis (UV) is a rare cutaneous vasculitis of small vessels characterized by recurrent episodes of wheal-like l …
Diagnosis and treatment of IgA nephropathy and IgA vasculitis nephritis in Chinese children.
Zhong X, Ding J. Zhong X, et al. Pediatr Nephrol. 2023 Jun;38(6):1707-1715. doi: 10.1007/s00467-022-05798-6. Epub 2022 Nov 8. Pediatr Nephrol. 2023. PMID: 36348077 Free PMC article. Review.
IgA nephropathy (IgAN) and IgA vasculitis-associated nephritis (IgAVN) are among the most frequent childhood glomerular diseases and are characterized by significant variability in clinical manifestations, pathological presentation and long-term outcomes. ...
IgA nephropathy (IgAN) and IgA vasculitis-associated nephritis (IgAVN) are among the most frequent childhood glomerular diseases and …
639 results