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

Year Number of Results
1951 1
1954 1
1955 1
1956 3
1959 2
1960 4
1962 1
1963 10
1964 27
1965 21
1966 13
1967 15
1968 21
1969 30
1970 25
1971 28
1972 25
1973 30
1974 35
1975 24
1976 32
1977 22
1978 32
1979 27
1980 40
1981 34
1982 42
1983 38
1984 42
1985 53
1986 41
1987 43
1988 41
1989 58
1990 69
1991 78
1992 52
1993 71
1994 65
1995 67
1996 57
1997 67
1998 55
1999 58
2000 65
2001 67
2002 73
2003 81
2004 59
2005 78
2006 85
2007 107
2008 97
2009 95
2010 87
2011 84
2012 91
2013 107
2014 99
2015 120
2016 101
2017 127
2018 106
2019 126
2020 114
2021 109
2022 49
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3,395 results
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ANCA-Associated Vasculitis: Core Curriculum 2020.
Geetha D, Jefferson JA. Geetha D, et al. Am J Kidney Dis. 2020 Jan;75(1):124-137. doi: 10.1053/j.ajkd.2019.04.031. Epub 2019 Jul 26. Am J Kidney Dis. 2020. PMID: 31358311 Review.
Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a group of disorders characterized by inflammation and destruction of small- and medium-sized blood vessels and the presence of circulating ANCA. Clinical disease phenotypes include granulomatosis
Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a group of disorders characterized by inflammation and dest …
ANCA Glomerulonephritis and Vasculitis.
Jennette JC, Nachman PH. Jennette JC, et al. Clin J Am Soc Nephrol. 2017 Oct 6;12(10):1680-1691. doi: 10.2215/CJN.02500317. Epub 2017 Aug 25. Clin J Am Soc Nephrol. 2017. PMID: 28842398 Free PMC article. Review.
Pauci-immune necrotizing and crescentic GN is a frequent component of ANCA vasculitis. ANCA vasculitis is associated with ANCA specific for myeloperoxidase (MPO-ANCA) or proteinase 3 (PR3-ANCA). ...To fully characterize a patient, the serotype also should be accompa …
Pauci-immune necrotizing and crescentic GN is a frequent component of ANCA vasculitis. ANCA vasculitis is associated with ANCA …
Clinic manifestations in granulomatosis with polyangiitis.
Greco A, Marinelli C, Fusconi M, Macri GF, Gallo A, De Virgilio A, Zambetti G, de Vincentiis M. Greco A, et al. Int J Immunopathol Pharmacol. 2016 Jun;29(2):151-9. doi: 10.1177/0394632015617063. Epub 2015 Dec 18. Int J Immunopathol Pharmacol. 2016. PMID: 26684637 Free PMC article. Review.
Granulomatosis with polyangiitis (GPA), formerly Wegener's granulomatosis (WG), is an uncommon immunologically mediated systemic small-vessel vasculitis that is pathologically characterised by an inflammatory reaction pattern (necrosis, granulomatous i
Granulomatosis with polyangiitis (GPA), formerly Wegener's granulomatosis (WG), is an uncommon immunologically mediated sys
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). ...
Eosinophilic granulomatosis with polyangiitis (EGPA, formerly Churg-Strauss syndrome) is the least frequent antineutrophil cytoplasm …
Epidemiology and management of interstitial lung disease in ANCA-associated vasculitis.
Sebastiani M, Manfredi A, Vacchi C, Cassone G, Faverio P, Cavazza A, Sverzellati N, Salvarani C, Luppi F. Sebastiani M, et al. Clin Exp Rheumatol. 2020 Mar-Apr;38 Suppl 124(2):221-231. Epub 2020 Apr 22. Clin Exp Rheumatol. 2020. PMID: 32324122 Free article. Review.
Antineutrophil cytoplasmic antibodies (ANCA)-associated vasculitis (AAV) is a group of systemic vasculitides that predominantly affect small vessels, including granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), and eosinophilic …
Antineutrophil cytoplasmic antibodies (ANCA)-associated vasculitis (AAV) is a group of systemic vasculitides that predo …
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 w …
ANCA-associated vasculitis with renal involvement.
Binda V, Moroni G, Messa P. Binda V, et al. J Nephrol. 2018 Apr;31(2):197-208. doi: 10.1007/s40620-017-0412-z. Epub 2017 May 30. J Nephrol. 2018. PMID: 28560688 Review.
Systemic vasculitis is a rare but severe group of diseases characterized by inflammation and necrosis of blood vessels. The size of the vessel affected varies among the different forms of vasculitis and there are three main subgroups: large, medium and small
Systemic vasculitis is a rare but severe group of diseases characterized by inflammation and necrosis of blood vessels. The si
Eosinophilic granulomatosis with polyangiitis (Churg-Strauss) (EGPA) Consensus Task Force recommendations for evaluation and management.
Groh M, Pagnoux C, Baldini C, Bel E, Bottero P, Cottin V, Dalhoff K, Dunogué B, Gross W, Holle J, Humbert M, Jayne D, Jennette JC, Lazor R, Mahr A, Merkel PA, Mouthon L, Sinico RA, Specks U, Vaglio A, Wechsler ME, Cordier JF, Guillevin L. Groh M, et al. Eur J Intern Med. 2015 Sep;26(7):545-53. doi: 10.1016/j.ejim.2015.04.022. Epub 2015 May 9. Eur J Intern Med. 2015. PMID: 25971154 Free article.
OBJECTIVE: To develop disease-specific recommendations for the diagnosis and management of eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome) (EGPA). METHODS: The EGPA Consensus Task Force experts comprised 8 pulmonologists, 6 internists, 4 rheumatologi …
OBJECTIVE: To develop disease-specific recommendations for the diagnosis and management of eosinophilic granulomatosis with polyangii …
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 …
Otopathology of Vasculitis in Granulomatosis With Polyangitis.
Santos F, Salviz M, Domond H, Nadol JB. Santos F, et al. Otol Neurotol. 2015 Dec;36(10):1657-62. doi: 10.1097/MAO.0000000000000868. Otol Neurotol. 2015. PMID: 26496669 Free PMC article.
OBJECTIVE: To describe the temporal bone histopathology of vasculitis in granulomatosis with polyangitis. BACKGROUND: Granulomatosis with polyangitis is an autoimmune disease that presents as granulomatosis and vasculitis. ...CONCL …
OBJECTIVE: To describe the temporal bone histopathology of vasculitis in granulomatosis with polyangitis. BACKGROUND: …
3,395 results