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1963
2025

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

Year Number of Results
1963 3
1964 6
1967 3
1968 3
1969 8
1970 6
1971 8
1972 7
1973 7
1974 10
1975 4
1976 12
1977 10
1978 8
1979 15
1980 15
1981 14
1982 9
1983 15
1984 12
1985 20
1986 15
1987 20
1988 24
1989 34
1990 33
1991 29
1992 44
1993 43
1994 53
1995 50
1996 47
1997 43
1998 38
1999 39
2000 46
2001 51
2002 43
2003 48
2004 57
2005 60
2006 63
2007 81
2008 72
2009 75
2010 65
2011 49
2012 73
2013 104
2014 77
2015 82
2016 59
2017 80
2018 78
2019 70
2020 77
2021 72
2022 61
2023 63
2024 47
2025 0

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2,195 results

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Page 1
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 gr …
Anti-neutrophil cytoplasmic antibody (ANCA) associated vasculitis (AAV) compromise a rare group of necrotizing small to medium …
Diagnosis and management of leukocytoclastic vasculitis.
Fraticelli P, Benfaremo D, Gabrielli A. Fraticelli P, et al. Intern Emerg Med. 2021 Jun;16(4):831-841. doi: 10.1007/s11739-021-02688-x. Epub 2021 Mar 13. Intern Emerg Med. 2021. PMID: 33713282 Free PMC article. Review.
Leukocytoclastic vasculitis (LCV) is a histopathologic description of a common form of small vessel vasculitis (SVV), that can be found in various types of vasculitis affecting the skin and internal organs. ...Among systemic diseases, the most frequently asso …
Leukocytoclastic vasculitis (LCV) is a histopathologic description of a common form of small vessel vasculitis (SVV), that can …
A Spotlight on Drug-Induced Vasculitis.
Yaseen K, Nevares A, Tamaki H. Yaseen K, et al. Curr Rheumatol Rep. 2022 Nov;24(11):323-336. doi: 10.1007/s11926-022-01088-0. Epub 2022 Sep 21. Curr Rheumatol Rep. 2022. PMID: 36129631 Review.
PURPOSE OF REVIEW: Drug-induced vasculitis (DIV) is a rare form of vasculitis related to the use of various drugs. DIV primarily affects small to medium size vessels, but it can potentially involve vessels of any size. Differentiating between primary systemic vas
PURPOSE OF REVIEW: Drug-induced vasculitis (DIV) is a rare form of vasculitis related to the use of various drugs. DIV primari …
ANCA-associated vasculitis-treatment standard.
Chalkia A, Jayne D. Chalkia A, et al. Nephrol Dial Transplant. 2024 May 31;39(6):944-955. doi: 10.1093/ndt/gfad237. Nephrol Dial Transplant. 2024. PMID: 37947275 Free PMC article. Review.
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) are characterized by small-vessel necrotizing inflammation, and prior to the advent of immunosuppressive therapy frequently had a fatal outcome. ...
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) are characterized by small-vessel necrotizing inflam …
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). In this review, we detail the fiv …
Lung involvement is one of the most common clinical features in ANCA-associated vasculitides (AAV), including granulomatosis with pol …
ANCA-associated vasculitis.
Yates M, Watts R. Yates M, et al. Clin Med (Lond). 2017 Feb;17(1):60-64. doi: 10.7861/clinmedicine.17-1-60. Clin Med (Lond). 2017. PMID: 28148583 Free PMC article. Review.
The vasculitides are a heterogeneous group of conditions typified by their ability to cause vessel inflammation with or without necrosis. ...The antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) are three separate conditions - granuloma …
The vasculitides are a heterogeneous group of conditions typified by their ability to cause vessel inflammation with or without ne
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 hallmark of vasculitis is autoimmune inflammation of blood vessels and surrounding tissues, resulting in an array of constitutional symptoms and organ damage. The lung is commonly targeted in the more familiar ANCA-associated small vessel vasculitidies, but large and m …
The hallmark of vasculitis is autoimmune inflammation of blood vessels and surrounding tissues, resulting in an array of constitution …
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 vasculiti
Eosinophilic granulomatosis with polyangiitis is a small to medium vessel necrotizing vasculitis, typically classified with gr …
Vasculitis therapy refines vasculitis mechanistic classification.
Torp CK, Brüner M, Keller KK, Brouwer E, Hauge EM, McGonagle D, Kragstrup TW. Torp CK, et al. Autoimmun Rev. 2021 Jun;20(6):102829. doi: 10.1016/j.autrev.2021.102829. Epub 2021 Apr 16. Autoimmun Rev. 2021. PMID: 33872767 Free article. Review.
The primary vasculitides constitute a heterogeneous group of immune mediated diseases of incompletely understood pathogenesis currently classified by the size of blood vessels affected (Chapel Hill classification). In recent years, several drugs with well-characterized imm …
The primary vasculitides constitute a heterogeneous group of immune mediated diseases of incompletely understood pathogenesis current …
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. ...A recent consensus algorithm for the classification of PAN has attempted to over …
Polyarteritis nodosa (PAN) is a systemic necrotizing vasculitis preferentially targeting medium-sized arteries and not associa …
2,195 results