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1962 5
1963 3
1964 5
1965 1
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1972 1
1973 1
1975 3
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1978 5
1979 1
1980 4
1981 5
1982 8
1983 7
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1985 13
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1992 41
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1994 59
1995 77
1996 44
1997 53
1998 74
1999 71
2000 85
2001 92
2002 88
2003 94
2004 89
2005 96
2006 94
2007 129
2008 139
2009 143
2010 147
2011 144
2012 171
2013 178
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4,505 results

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Page 1
Eosinophilic granulomatosis with polyangiitis: A review.
White J, Dubey S. White J, et al. Autoimmun Rev. 2023 Jan;22(1):103219. doi: 10.1016/j.autrev.2022.103219. Epub 2022 Oct 22. Autoimmun Rev. 2023. PMID: 36283646 Free article. Review.
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare, multi-system, inflammatory disease, belonging to the group of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV). Previously known as Churg-Strauss
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare, multi-system, inflammatory disease, belonging to
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.
This review aims to describe the epidemiology, pathogenesis, clinical manifestations, diagnosis, treatment, and prognosis of eosinophilic granulomatosis with polyangiitis (EGPA). Eosinophilic granulomatosis with polyangiitis
This review aims to describe the epidemiology, pathogenesis, clinical manifestations, diagnosis, treatment, and prognosis of eosinophilic
Eosinophilic granulomatosis with polyangiitis: understanding the disease and its management.
Trivioli G, Terrier B, Vaglio A. Trivioli G, et al. Rheumatology (Oxford). 2020 May 1;59(Suppl 3):iii84-iii94. doi: 10.1093/rheumatology/kez570. Rheumatology (Oxford). 2020. PMID: 32348510 Review.
Eosinophilic granulomatosis with polyangiitis is characterized by asthma, blood and tissue eosinophilia and small-vessel vasculitis. ...Eosinophilic granulomatosis with polyangiitis must be differentiated from several condit
Eosinophilic granulomatosis with polyangiitis is characterized by asthma, blood and tissue eosinophilia and smal
Eosinophilic granulomatosis with polyangiitis.
Romero Gómez C, Hernández Negrín H, Ayala Gutiérrez MDM. Romero Gómez C, et al. Med Clin (Barc). 2023 Apr 6;160(7):310-317. doi: 10.1016/j.medcli.2023.01.003. Epub 2023 Feb 9. Med Clin (Barc). 2023. PMID: 36774291 Review. English, Spanish.
Eosinophilic granulomatosis with polyangiitis (EGPA) is a systemic vasculitis characterized by the presence of asthma associated with eosinophilia, eosinophilic infiltration of different organs, and vasculitis of small and medium-sized vessels.
Eosinophilic granulomatosis with polyangiitis (EGPA) is a systemic vasculitis characterized by the presence of a
EOSINOPHILIC GRANULOMATOSIS WITH POLYANGIITIS INDUCED BY MONTELUKAST.
Grama P, Ureche C, Zah CA, Buzoianu AD, Bocsan IC. Grama P, et al. Acta Clin Croat. 2024 Apr;63(1):45-54. doi: 10.20471/acc.2024.63.01.6. Acta Clin Croat. 2024. PMID: 39959324 Free PMC article. Review.
Among the adverse effects induced by them, particularly by montelukast, is eosinophilic granulomatosis with polyangiitis (EGPA), which manifests as a form of vasculitis co-occurring with severe asthma and eosinophilia. ...
Among the adverse effects induced by them, particularly by montelukast, is eosinophilic granulomatosis with polyangi
Unmet needs and evidence gaps in hypereosinophilic syndrome and eosinophilic granulomatosis with polyangiitis.
Wechsler ME, Hellmich B, Cid MC, Jayne D, Tian X, Baylis L, Roufosse F. Wechsler ME, et al. J Allergy Clin Immunol. 2023 Jun;151(6):1415-1428. doi: 10.1016/j.jaci.2023.03.011. Epub 2023 Apr 21. J Allergy Clin Immunol. 2023. PMID: 37086239 Free article. Review.
Hypereosinophilic syndrome (HES) and eosinophilic granulomatosis with polyangiitis (EGPA) are rare systemic inflammatory disorders with overlapping symptoms, elevated eosinophil counts, and heterogenous clinical presentations. ...
Hypereosinophilic syndrome (HES) and eosinophilic granulomatosis with polyangiitis (EGPA) are rare system …
Eosinophilic granulomatosis with polyangiitis: Cutaneous clinical and histopathologic differential diagnosis.
Tabb ES, Duncan LM, Nazarian RM. Tabb ES, et al. J Cutan Pathol. 2021 Nov;48(11):1379-1386. doi: 10.1111/cup.14065. Epub 2021 Jun 6. J Cutan Pathol. 2021. PMID: 34019312 Review.
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare, but severe systemic vasculitis that can affect skin and other organ systems. ...According to the EGPA Consensus Task Force recommendations, EGPA is a syndrome of asthma, eosinophili
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare, but severe systemic vasculitis that can affect s
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. ...That finding opens a new era in eosinophilic granulomatosis
Eosinophilic granulomatosis with polyangiitis (formerly Churg-Strauss syndrome) is a rare t
Eosinophilic granulomatosis with polyangiitis: current status and future perspectives.
Kamide Y, Taniguchi M. Kamide Y, et al. Respir Investig. 2025 Jul;63(4):639-650. doi: 10.1016/j.resinv.2025.04.018. Epub 2025 May 17. Respir Investig. 2025. PMID: 40383090 Review.
Eosinophilic granulomatosis with polyangiitis (EGPA) is a systemic vasculitis with hypereosinophilia that is preceded by asthma and chronic rhinosinusitis with nasal polyps. ...
Eosinophilic granulomatosis with polyangiitis (EGPA) is a systemic vasculitis with hypereosinophilia that is pre
[Eosinophilic granulomatosis with polyangiitis : Update on classification and management].
Hellmich B, Holle J, Moosig F. Hellmich B, et al. Z Rheumatol. 2022 May;81(4):286-299. doi: 10.1007/s00393-021-01153-6. Epub 2022 Jan 24. Z Rheumatol. 2022. PMID: 35075511 Review. German.
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare chronic inflammatory systemic disease that occurs in patients with bronchial asthma and is associated with significant blood and tissue eosinophilia. ...
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare chronic inflammatory systemic disease that occurs
4,505 results