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Quoted phrase not found in phrase index: "Pauci-Immune Glomerulonephritis associated with Eosinophilic Granulomatosis with Polyangiitis"
Page 1
Pauci-immune crescentic glomerulonephritis.
Gupta RK. Gupta RK. Indian J Pathol Microbiol. 2003 Jul;46(3):357-66. Indian J Pathol Microbiol. 2003. PMID: 15025274 Review.
Pauci-immune crescentic glomerulonephritis (PICGN) is a rapidly progressive condition leading to renal failure within days or weeks and is potentially life threatening. ...PICGN may occur as renal limited disease or as a component of systemic necrotising smal …
Pauci-immune crescentic glomerulonephritis (PICGN) is a rapidly progressive condition leading to renal failure within d …
Pauci-immune necrotizing glomerulonephritis.
Rutgers A, Sanders JS, Stegeman CA, Kallenberg CG. Rutgers A, et al. Rheum Dis Clin North Am. 2010 Aug;36(3):559-72. doi: 10.1016/j.rdc.2010.05.002. Rheum Dis Clin North Am. 2010. PMID: 20688250 Review.
Pauci-immune necrotizing glomerulonephritis is the most frequent cause of rapidly progressive glomerulonephritis and, in most cases, is associated with antineutrophil cytoplasmic antibodies (ANCA). It is either the renal manifestation of Wegener …
Pauci-immune necrotizing glomerulonephritis is the most frequent cause of rapidly progressive glomerulonephritis …
Histopathological classification of pauci-immune glomerulonephritis and its impact on outcome.
Naidu GS, Sharma A, Nada R, Kohli HS, Jha V, Gupta KL, Sakhuja V, Rathi M. Naidu GS, et al. Rheumatol Int. 2014 Dec;34(12):1721-7. doi: 10.1007/s00296-014-3041-z. Epub 2014 May 18. Rheumatol Int. 2014. PMID: 24838685
Rapidly progressive renal failure is a common but severe feature of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis. A histopathological classification for ANCA-associated pauci-immune glomerulonephritis was developed for pro …
Rapidly progressive renal failure is a common but severe feature of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis. …
The diagnostic and prognostic significance of ANCA.
Lesavre P. Lesavre P. Ren Fail. 1996 Sep;18(5):803-12. doi: 10.3109/08860229609047708. Ren Fail. 1996. PMID: 8903094 Review.
Antineutrophil cytoplasmic antibodies (ANCA) constitute a family of auto-antibodies directed against various components of the neutrophil cytoplasm. Their identification and association with vasculitis and rapidly progressive glomerulonephritis has led to considerin …
Antineutrophil cytoplasmic antibodies (ANCA) constitute a family of auto-antibodies directed against various components of the neutrophil cy …
Renal involvement in anti-neutrophil cytoplasmic autoantibody associated vasculitis.
Sinico RA, Di Toma L, Radice A. Sinico RA, et al. Autoimmun Rev. 2013 Feb;12(4):477-82. doi: 10.1016/j.autrev.2012.08.006. Epub 2012 Aug 16. Autoimmun Rev. 2013. PMID: 22921791 Review.
Renal involvement is a common and often severe complication of anti-neutrophil cytoplasmic autoantibody (ANCA) associated vasculitides (AAV). With the exception of Churg-Strauss syndrome (CSS), where kidney involvement is not a prominent feature, renal …
Renal involvement is a common and often severe complication of anti-neutrophil cytoplasmic autoantibody (ANCA) associated vasculitide …
ANCA glomerulonephritis and vasculitis: a Chapel Hill perspective.
Falk RJ, Nachman PH, Hogan SL, Jennette JC. Falk RJ, et al. Semin Nephrol. 2000 May;20(3):233-43. Semin Nephrol. 2000. PMID: 10855933 Review.
Microscopic polyangiitis, Wegener's granulomatosis, Churg-Strauss syndrome, and pauci-immune necrotizing glomerulonephritis share pathogenic, pathological, and clinical features. ...The renal manifestations can present as a …
Microscopic polyangiitis, Wegener's granulomatosis, Churg-Strauss syndrome, and pauci-immune …
Simultaneous development of IgA vasculitis and eosinophilic granulomatosis with polyangiitis.
Asano Y, Matsumoto Y, Miyazaki T, Ishizu A, Morizane S, Hayashi K, Yamamura Y, Hiramatsu S, Miyawaki Y, Morishita M, Ohashi K, Watanabe H, Watanabe KS, Kawabata T, Sada KE, Makino H, Wada J. Asano Y, et al. Mod Rheumatol Case Rep. 2020 Jan;4(1):63-69. doi: 10.1080/24725625.2019.1673528. Epub 2019 Oct 23. Mod Rheumatol Case Rep. 2020. PMID: 33086980
Eosinophilic granulomatosis with polyangiitis (EGPA) is an anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) characterised by eosinophil-rich and granulomatous inflammation in small to medium-sized vessels. ...Our case provides ev …
Eosinophilic granulomatosis with polyangiitis (EGPA) is an anti-neutrophil cytoplasmic antibody (ANCA)-associated …
The appropriate use of antineutrophil cytoplasmic antibody (ANCA) testing in rheumatic diseases.
Teo DL. Teo DL. Ann Acad Med Singap. 1998 Jan;27(1):54-60. Ann Acad Med Singap. 1998. PMID: 9588276 Review.
Improvement, simplification and standardisation of the testing methodology have enabled it to become more reliable and accessible to clinicians. ANCA has strong association with and is most useful in the diagnosis and management of the ANCA-associated vasculitides w …
Improvement, simplification and standardisation of the testing methodology have enabled it to become more reliable and accessible to clinici …
Early Outcomes in Children With Antineutrophil Cytoplasmic Antibody-Associated Vasculitis.
Morishita KA, Moorthy LN, Lubieniecka JM, Twilt M, Yeung RSM, Toth MB, Shenoi S, Ristic G, Nielsen SM, Luqmani RA, Li SC, Lee T, Lawson EF, Kostik MM, Klein-Gitelman M, Huber AM, Hersh AO, Foell D, Elder ME, Eberhard BA, Dancey P, Charuvanij S, Benseler SM, Cabral DA; ARChiVe Investigators Network within the PedVas Initiative. Morishita KA, et al. Arthritis Rheumatol. 2017 Jul;69(7):1470-1479. doi: 10.1002/art.40112. Epub 2017 Jun 9. Arthritis Rheumatol. 2017. PMID: 28371513
OBJECTIVE: To characterize the early disease course in childhood-onset antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) and the 12-month outcomes in children with AAV. METHODS: Eligible subjects were children entered into the Pediatric Vasculit …
OBJECTIVE: To characterize the early disease course in childhood-onset antineutrophil cytoplasmic antibody (ANCA)-associated v …
Eosinophilic granulomatosis with polyangiitis in a continuous flow left ventricular assist device patient: a case report and review of literature.
Engwenyu LR, Tchakarov A, Zhao B. Engwenyu LR, et al. Cardiovasc Pathol. 2019 Mar-Apr;39:70-73. doi: 10.1016/j.carpath.2018.12.004. Epub 2018 Dec 28. Cardiovasc Pathol. 2019. PMID: 30684748 Review.
Eosinophilic granulomatosis with polyangiitis (EGPA), also known as Churg-Strauss syndrome (CSS), is a rare autoimmune disease with an estimated incidence of approximately 0.11 to 2.66 new cases per 1 million people per year and an overal …
Eosinophilic granulomatosis with polyangiitis (EGPA), also known as Churg-Strauss syndrome (CSS), …
17 results