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

Year Number of Results
1950 1
1970 2
1971 1
1974 1
1975 6
1976 5
1977 5
1978 3
1979 3
1980 4
1981 5
1982 2
1983 1
1984 6
1985 4
1986 5
1987 11
1988 8
1989 13
1990 23
1991 26
1992 26
1993 31
1994 27
1995 42
1996 36
1997 43
1998 28
1999 38
2000 49
2001 42
2002 41
2003 47
2004 36
2005 64
2006 64
2007 54
2008 64
2009 75
2010 89
2011 116
2012 103
2013 147
2014 123
2015 116
2016 101
2017 107
2018 113
2019 102
2020 136
2021 167
2022 164
2023 154
2024 71

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2,439 results

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Page 1
EULAR recommendations for the management of ANCA-associated vasculitis: 2022 update.
Hellmich B, Sanchez-Alamo B, Schirmer JH, Berti A, Blockmans D, Cid MC, Holle JU, Hollinger N, Karadag O, Kronbichler A, Little MA, Luqmani RA, Mahr A, Merkel PA, Mohammad AJ, Monti S, Mukhtyar CB, Musial J, Price-Kuehne F, Segelmark M, Teng YKO, Terrier B, Tomasson G, Vaglio A, Vassilopoulos D, Verhoeven P, Jayne D. Hellmich B, et al. Ann Rheum Dis. 2024 Jan 2;83(1):30-47. doi: 10.1136/ard-2022-223764. Ann Rheum Dis. 2024. PMID: 36927642
BACKGROUND: Since the publication of the EULAR recommendations for the management of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) in 2016, several randomised clinical trials have been published that have the potential to change clinical care and s …
BACKGROUND: Since the publication of the EULAR recommendations for the management of antineutrophil cytoplasmic antibody (ANCA)-associated …
ANCA-associated vasculitis.
Kitching AR, Anders HJ, Basu N, Brouwer E, Gordon J, Jayne DR, Kullman J, Lyons PA, Merkel PA, Savage COS, Specks U, Kain R. Kitching AR, et al. Nat Rev Dis Primers. 2020 Aug 27;6(1):71. doi: 10.1038/s41572-020-0204-y. Nat Rev Dis Primers. 2020. PMID: 32855422 Free article. Review.
The anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAVs) are a group of disorders involving severe, systemic, small-vessel vasculitis and are characterized by the development of autoantibodies to the neutrophil proteins leukocyte proteinase 3 ( …
The anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAVs) are a group of disorders involving severe, systemic, s …
Treatment Guidelines in Vasculitis.
Kermani TA, Warrington KJ, Dua AB. Kermani TA, et al. Rheum Dis Clin North Am. 2022 Aug;48(3):705-724. doi: 10.1016/j.rdc.2022.03.006. Epub 2022 Jul 5. Rheum Dis Clin North Am. 2022. PMID: 35953232 Review.
The different forms are commonly classified based on the size of the blood vessel involved as large-vessel, medium-vessel, and small-vessel vasculitis. The American College of Rheumatology/Vasculitis Foundation recently published guidelines on the management of seve …
The different forms are commonly classified based on the size of the blood vessel involved as large-vessel, medium-vessel, and small-vessel …
Eosinophilic granulomatosis with polyangiitis.
Villa-Forte A. Villa-Forte A. Postgrad Med. 2023 Jan;135(sup1):52-60. doi: 10.1080/00325481.2022.2134624. Epub 2022 Dec 5. Postgrad Med. 2023. PMID: 36259957 Review.
Eosinophilic granulomatosis with polyangiitis is a small to medium vessel necrotizing vasculitis, typically classified with granulomatosis with polyangiitis (GPA) and microscopic polyangitis (MPA) as antineutrophil cytoplasmic antibody (ANCA)-associated va …
Eosinophilic granulomatosis with polyangiitis is a small to medium vessel necrotizing vasculitis, typically classified with granuloma …
Diagnosing and treating ANCA-associated vasculitis: an updated review for clinical practice.
Chevet B, Cornec D, Casal Moura M, Cornec-Le Gall E, Fervenza FC, Warrington KJ, Specks U, Berti A. Chevet B, et al. Rheumatology (Oxford). 2023 May 2;62(5):1787-1803. doi: 10.1093/rheumatology/keac623. Rheumatology (Oxford). 2023. PMID: 36315063 Review.
ANCA-associated vasculitides (AAV) are a group of rare, primary, systemic necrotizing small-vessel vasculitides. Granulomatosis with polyangiitis and microscopic polyangiitis account for 80-90% of all AAV. ...
ANCA-associated vasculitides (AAV) are a group of rare, primary, systemic necrotizing small-vessel vasculitides. Granulomatosis with …
ANCA associated vasculitis (AAV): a review for internists.
Yaseen K, Mandell BF. Yaseen K, et al. Postgrad Med. 2023 Jan;135(sup1):3-13. doi: 10.1080/00325481.2022.2102368. Epub 2022 Jul 21. Postgrad Med. 2023. PMID: 35831990 Review.
Anti-neutrophil cytoplasmic antibody (ANCA) associated vasculitis (AAV) compromise a rare group of necrotizing small to medium vessel vasculitides that constitute three distinct disorders: granulomatosis with polyangiitis (GPA) (formerly known as Wegener's granulomatosis), …
Anti-neutrophil cytoplasmic antibody (ANCA) associated vasculitis (AAV) compromise a rare group of necrotizing small to medium vessel …
Lung involvement in ANCA-associated vasculitis.
Sacoto G, Boukhlal S, Specks U, Flores-Suárez LF, Cornec D. Sacoto G, et al. Presse Med. 2020 Oct;49(3):104039. doi: 10.1016/j.lpm.2020.104039. Epub 2020 Jul 7. Presse Med. 2020. PMID: 32650042 Review.
Lung involvement is one of the most common clinical features in ANCA-associated vasculitides (AAV), including granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), and eosinophilic granulomatosis with polyangiitis (EGPA). ...
Lung involvement is one of the most common clinical features in ANCA-associated vasculitides (AAV), including granulomatosis with polyangiit …
Diagnosis and management of ANCA-associated vasculitis.
Kronbichler A, Bajema IM, Bruchfeld A, Mastroianni Kirsztajn G, Stone JH. Kronbichler A, et al. Lancet. 2024 Feb 17;403(10427):683-698. doi: 10.1016/S0140-6736(23)01736-1. Lancet. 2024. PMID: 38368016 Review.
Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis consists of two main diseases, granulomatosis with polyangiitis and microscopic polyangiitis, and remains among the most devastating and potentially lethal forms of autoimmune inflammatory disease. Gra …
Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis consists of two main diseases, granulomatosis with polyangiitis and …
Position paper: Revised 2017 international consensus on testing of ANCAs in granulomatosis with polyangiitis and microscopic polyangiitis.
Bossuyt X, Cohen Tervaert JW, Arimura Y, Blockmans D, Flores-Suárez LF, Guillevin L, Hellmich B, Jayne D, Jennette JC, Kallenberg CGM, Moiseev S, Novikov P, Radice A, Savige JA, Sinico RA, Specks U, van Paassen P, Zhao MH, Rasmussen N, Damoiseaux J, Csernok E. Bossuyt X, et al. Nat Rev Rheumatol. 2017 Nov;13(11):683-692. doi: 10.1038/nrrheum.2017.140. Epub 2017 Sep 14. Nat Rev Rheumatol. 2017. PMID: 28905856 Review.
Anti-neutrophil cytoplasmic antibodies (ANCAs) are valuable laboratory markers used for the diagnosis of well-defined types of small-vessel vasculitis, including granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA). ...As dependable immunoassays …
Anti-neutrophil cytoplasmic antibodies (ANCAs) are valuable laboratory markers used for the diagnosis of well-defined types of small-vessel …
Microscopic polyangiitis.
Tobiáš D, Brázdilová K, Killinger Z, Payer J. Tobiáš D, et al. Vnitr Lek. 2020 Summer;66(4):249-252. Vnitr Lek. 2020. PMID: 32972189 English.
Microscopic polyangiitis is a rare, systemic, necrotizing, pauci-immune, ANCA associated small vessel vasculitis, with no evidence of granulomatous inflammation. Diagnosing microscopic polyangiitis is often difficult because of its presentation by a nu …
Microscopic polyangiitis is a rare, systemic, necrotizing, pauci-immune, ANCA associated small vessel vasculitis, with …
2,439 results