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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 94
2010 87
2011 84
2012 90
2013 107
2014 99
2015 120
2016 100
2017 127
2018 105
2019 121
2020 50
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3,204 results
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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
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 …
Treatment of Eosinophilic Granulomatosis with Polyangiitis: A Review.
Raffray L, Guillevin L. Raffray L, et al. Drugs. 2018 Jun;78(8):809-821. doi: 10.1007/s40265-018-0920-8. Drugs. 2018. PMID: 29766394 Review.
Eosinophilic granulomatosis with polyangiitis (formerly Churg-Strauss syndrome) is a rare type of anti-neutrophil cytoplasm antibody-associated vasculitis. Nevertheless, eosinophilic granulomatosis with polyangiitis stands apart because it has features of …
Eosinophilic granulomatosis with polyangiitis (formerly Churg-Strauss syndrome) is a rare type of anti-neutrophil cytoplasm antibody- …
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: …
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 …
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 …
Efficacy and safety of rituximab in the treatment of eosinophilic granulomatosis with polyangiitis.
Teixeira V, Mohammad AJ, Jones RB, Smith R, Jayne D. Teixeira V, et al. RMD Open. 2019 Jun 5;5(1):e000905. doi: 10.1136/rmdopen-2019-000905. eCollection 2019. RMD Open. 2019. PMID: 31245051 Free PMC article.
INTRODUCTION: Eosinophilic granulomatosis with polyangiitis (EGPA) is a subset of antineutrophil cytoplasmic antibodies (ANCA) associated vasculitis with distinct pathophysiological mechanisms, clinical features and treatment responses. Rituximab is a licensed thera …
INTRODUCTION: Eosinophilic granulomatosis with polyangiitis (EGPA) is a subset of antineutrophil cytoplasmic antibodies (ANCA) associ …
Eosinophilic Granulomatosis with Polyangiitis: Clinical Pathology Conference and Review.
Wu EY, Hernandez ML, Jennette JC, Falk RJ. Wu EY, et al. J Allergy Clin Immunol Pract. 2018 Sep-Oct;6(5):1496-1504. doi: 10.1016/j.jaip.2018.07.001. J Allergy Clin Immunol Pract. 2018. PMID: 30197069 Review.
Eosinophilic granulomatosis with polyangiitis (EGPA) (formerly Churg-Strauss syndrome) is a small vessel vasculitis associated with asthma and eosinophilia. ...EGPA is also a conceptually difficult disorder given its dual categorization with hypereosinophilic syndro …
Eosinophilic granulomatosis with polyangiitis (EGPA) (formerly Churg-Strauss syndrome) is a small vessel vasculitis associated …
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
One year in review 2018: systemic vasculitis.
Elefante E, Bond M, Monti S, Lepri G, Cavallaro E, Felicetti M, Calabresi E, Posarelli C, Talarico R, Quartuccio L, Baldini C. Elefante E, et al. Clin Exp Rheumatol. 2018 Mar-Apr;36 Suppl 111(2):12-32. Epub 2018 May 18. Clin Exp Rheumatol. 2018. PMID: 29799395 Free article. Review.
Systemic vasculitis are heterogeneous, complex and disabling disorders. Following the previous annual reviews of this series, this paper gives a brief overview on current knowledge about recent literature on small- and large-vessel systemic vasculitis,
Systemic vasculitis are heterogeneous, complex and disabling disorders. Following the previous annual reviews of this series,
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