Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1993 1
1996 1
1998 1
1999 1
2000 1
2001 3
2002 1
2003 2
2004 1
2005 4
2006 4
2007 2
2009 2
2010 3
2011 1
2012 4
2013 3
2014 5
2015 2
2016 1
2017 4
2018 1
2019 1
2020 1
2021 1
2022 5
2023 3
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

51 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Pauci-Immune Glomerulonephritis associated with Microscopic Polyangiitis"
Page 1
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. ...To fully characterize a patient, the serotype also should be accompanied by the clinicopathologic variant if this can be determined: microscopic polyangiitis, gra …
Pauci-immune necrotizing and crescentic GN is a frequent component of ANCA vasculitis. ...To fully characterize a patient, the …
2022 American College of Rheumatology/European Alliance of Associations for Rheumatology classification criteria for microscopic polyangiitis.
Suppiah R, Robson JC, Grayson PC, Ponte C, Craven A, Khalid S, Judge A, Hutchings A, Merkel PA, Luqmani RA, Watts RA; DCVAS INVESTIGATORS. Suppiah R, et al. Ann Rheum Dis. 2022 Mar;81(3):321-326. doi: 10.1136/annrheumdis-2021-221796. Epub 2022 Feb 2. Ann Rheum Dis. 2022. PMID: 35110332
OBJECTIVE: To develop and validate classification criteria for microscopic polyangiitis (MPA). METHODS: Patients with vasculitis or comparator diseases were recruited into an international cohort. ...The final criteria and their weights were as follows: perinuclear …
OBJECTIVE: To develop and validate classification criteria for microscopic polyangiitis (MPA). METHODS: Patients with vasculit …
2022 American College of Rheumatology/European Alliance of Associations for Rheumatology Classification Criteria for Microscopic Polyangiitis.
Suppiah R, Robson JC, Grayson PC, Ponte C, Craven A, Khalid S, Judge A, Hutchings A, Merkel PA, Luqmani RA, Watts RA; DCVAS Study Group. Suppiah R, et al. Arthritis Rheumatol. 2022 Mar;74(3):400-406. doi: 10.1002/art.41983. Epub 2022 Feb 2. Arthritis Rheumatol. 2022. PMID: 35106973
OBJECTIVE: To develop and validate classification criteria for microscopic polyangiitis (MPA). METHODS: Patients with vasculitis or comparator diseases were recruited into an international cohort. ...The final criteria and their weights were as follows: perinuclear …
OBJECTIVE: To develop and validate classification criteria for microscopic polyangiitis (MPA). METHODS: Patients with vasculit …
Microscopic polyangiitis.
Tobiáš D, Brázdilová K, Killinger Z, Payer J. Tobiáš D, et al. Vnitr Lek. 2020 Summer;66(4):249-252. Vnitr Lek. 2020. PMID: 32972189 English.
Microscopic polyangiitis is a rare, systemic, necrotizing, pauci-immune, ANCA associated small vessel vasculitis, with no evidence of granulomatous inflammation. Diagnosing microscopic polyangiitis is often difficult because of its …
Microscopic polyangiitis is a rare, systemic, necrotizing, pauci-immune, ANCA associated small vessel vas …
The diagnosis and classification of microscopic polyangiitis.
Kallenberg CG. Kallenberg CG. J Autoimmun. 2014 Feb-Mar;48-49:90-3. doi: 10.1016/j.jaut.2014.01.023. Epub 2014 Jan 22. J Autoimmun. 2014. PMID: 24461388 Review.
Not all patients, however, have ANCA. Microscopic polyangiitis (MPA) belongs to the anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides. ...Renal involvement, which can be the only manifestation, is clinically apparent as rapidly progressive …
Not all patients, however, have ANCA. Microscopic polyangiitis (MPA) belongs to the anti-neutrophil cytoplasmic antibody (ANCA …
ANCA-associated pauci-immune glomerulonephritis: always pauci-immune?
Scaglioni V, Scolnik M, Catoggio LJ, Christiansen SB, Varela CF, Greloni G, Rosa-Diez G, Soriano ER. Scaglioni V, et al. Clin Exp Rheumatol. 2017 Mar-Apr;35 Suppl 103(1):55-58. Epub 2017 Jan 31. Clin Exp Rheumatol. 2017. PMID: 28229825
OBJECTIVES: Anti-neutrophil cytoplasmic antibody (ANCA)-associated glomerulonephritis (GN) is considered "pauci-immune" with absent or mild glomerular tuft staining for immunoglobulin (Ig) and/or complement. ...We determined to evaluate the prevalence …
OBJECTIVES: Anti-neutrophil cytoplasmic antibody (ANCA)-associated glomerulonephritis (GN) is considered "pauci-immu …
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 …
Renal Involvement in Antineutrophil Cytoplasmic Antibody-Associated Vasculitis.
Zonozi R, Niles JL, Cortazar FB. Zonozi R, et al. Rheum Dis Clin North Am. 2018 Nov;44(4):525-543. doi: 10.1016/j.rdc.2018.06.001. Epub 2018 Sep 7. Rheum Dis Clin North Am. 2018. PMID: 30274621 Review.
Antineutrophil cytoplasmic antibody-associated vasculitis (AAV) is the most common cause of rapidly progressive glomerulonephritis. ANCAs play an important role in the pathogenesis and diagnosis of AAV. The classic renal lesion in AAV is a pauci-immune …
Antineutrophil cytoplasmic antibody-associated vasculitis (AAV) is the most common cause of rapidly progressive glomerulonephritis …
Antineutrophil cytoplasmic antibodies.
Bosch X, Guilabert A, Font J. Bosch X, et al. Lancet. 2006 Jul 29;368(9533):404-18. doi: 10.1016/S0140-6736(06)69114-9. Lancet. 2006. PMID: 16876669 Review.
Much like other autoantibodies (eg, anti-double stranded DNA in systemic lupus erythematosus or antiglomerular basement membrane antibodies in Goodpasture's syndrome), antineutrophil cytoplasmic antibodies (ANCA) have provided doctors with a useful serological test to assist in d …
Much like other autoantibodies (eg, anti-double stranded DNA in systemic lupus erythematosus or antiglomerular basement membrane antibodies …
ANCA-associated vasculitis: diagnosis, clinical characteristics and treatment.
Haubitz M. Haubitz M. Vasa. 2007 May;36(2):81-9. doi: 10.1024/0301-1526.36.2.81. Vasa. 2007. PMID: 17708098 Review.
Small vessel vasculitides comprise the largest subgroup divided into diseases with a pauci-immune vasculitis and ANCA and diseases with deposition of immunoglobulin without ANCA. ANCA-associated systemic vasculitides include Wegener's granulomatosis, micro …
Small vessel vasculitides comprise the largest subgroup divided into diseases with a pauci-immune vasculitis and ANCA and dise …
51 results