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

Year Number of Results
1955 3
1957 2
1959 1
1962 2
1965 5
1966 6
1967 12
1968 25
1969 16
1970 25
1971 43
1972 46
1973 40
1974 57
1975 55
1976 82
1977 80
1978 99
1979 135
1980 97
1981 111
1982 135
1983 145
1984 130
1985 127
1986 123
1987 129
1988 96
1989 149
1990 190
1991 180
1992 181
1993 259
1994 239
1995 203
1996 201
1997 226
1998 221
1999 206
2000 210
2001 205
2002 201
2003 281
2004 223
2005 307
2006 286
2007 300
2008 345
2009 311
2010 276
2011 331
2012 359
2013 415
2014 363
2015 327
2016 281
2017 339
2018 272
2019 140
2020 3
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9,176 results
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Page 1
One year in review 2018: systemic vasculitis.
Elefante E, et al. Clin Exp Rheumatol 2018 - Review. PMID 29799395 Free article.
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, with a specific focus on pathogenetic and clinical aspects, novel possible disease-related biomarkers and current and future therapies that are in the pipeline....
Systemic vasculitis are heterogeneous, complex and disabling disorders. Following the previous annual reviews of this series, this pa …
Pulmonary vasculitis.
Lally L and Spiera RF. Rheum Dis Clin North Am 2015 - Review. PMID 25836645
Pulmonary vasculitis encompasses inflammation in the pulmonary vasculature with involved vessels varying in caliber from large elastic arteries to capillaries. Small pulmonary capillaries are the vessels most commonly involved in vasculitis affecting the lung. The antineutrophil cytoplasmic antibody-associated vasculitides, which include granulomatosis with polyangiitis (formerly Wegener granulomatosis), microscopic polyangiitis, and eosinophilic granulomatosis with polyangiitis (formerly Churg-Strauss syndrome), are the small vessel vasculitides in which pulmonary vasculitis is most frequently observed and are the major focus of this review. ...
Pulmonary vasculitis encompasses inflammation in the pulmonary vasculature with involved vessels varying in caliber from large elasti …
How Should We Classify Kawasaki Disease?
Marrani E, et al. Front Immunol 2018 - Review. PMID 30619331 Free PMC article.
Rheumatologists have classified it as a systemic vasculitis, while some immunologists have stressed the robust nature of the innate immune response that causes both systemic inflammation as well as damage to the coronary arterial wall and questioned whether KD falls within the spectrum of autoinflammatory diseases. ...
Rheumatologists have classified it as a systemic vasculitis, while some immunologists have stressed the robust nature of the innate i …
COGAN'S SYNDROME
Iliescu DA, et al. Rom J Ophthalmol 2015 - Review. PMID 27373108 Free PMC article.
CONCLUSIONS: Cogan's syndrome is a rare autoimmune vasculitis, with unknown pathogenesis. Infection was thought to have played a role in the pathogenesis of the disease, but now the autoimmunity hypothesis is considered more likely to be true. ...Approximately 70% of the patients have systemic disease, of which vasculitis is considered the pathological mechanism. Corticosteroids are the first line of treatment; multiple immunosuppressive drugs were also used with varying degrees of success. ...
CONCLUSIONS: Cogan's syndrome is a rare autoimmune vasculitis, with unknown pathogenesis. Infection was thought to have played a role …
Complement in ANCA-associated vasculitis: mechanisms and implications for management.
Chen M, et al. Nat Rev Nephrol 2017 - Review. PMID 28316335
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a group of potentially life-threatening autoimmune diseases. ...
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a group of potentially life-threatening autoimmune disease …
Position paper: Revised 2017 international consensus on testing of ANCAs in granulomatosis with polyangiitis and microscopic polyangiitis
Bossuyt X, et al. Nat Rev Rheumatol 2017 - Review. PMID 28905856
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 for PR3-ANCAs and MPO-ANCAs have become broadly available, there is increasing international agreement that high-quality immunoassays are the preferred screening method for the diagnosis of ANCA-associated vasculitis. ...
Anti-neutrophil cytoplasmic antibodies (ANCAs) are valuable laboratory markers used for the diagnosis of well-defined types of small-vessel …
Vasculitis: Decade in Review.
Demir S, et al. Curr Rheumatol Rev 2019 - Review. PMID 30047330
Description of the monogenic forms of vasculitis, such as deficiency of adenosine deaminase type 2 (DADA2), Haploinsufficiency of A20 (HA20), have introduced a new perspective to vasculopathies, and introduced alternative treatments for these diseases. ...
Description of the monogenic forms of vasculitis, such as deficiency of adenosine deaminase type 2 (DADA2), Haploinsufficiency of A20 …
The utility of the ACR/EULAR 2017 provisional classification criteria for granulomatosis with polyangiitis in Korean patients with antineutrophil cytoplasmic antibody-associated vasculitis.
Yoo J, et al. Clin Exp Rheumatol 2018. PMID 29185957
OBJECTIVES: We applied the ACR/EULAR 2017 provisional classification criteria for granulomatosis with polyangiitis (GPA) to 150 Korean patients with previously diagnosed antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) and investigated how many patients with AAV were reclassified as GPA. ...
OBJECTIVES: We applied the ACR/EULAR 2017 provisional classification criteria for granulomatosis with polyangiitis (GPA) to 150 Korean patie …
Approach to cutaneous vasculitides with special emphasis on small vessel vasculitis: histopathology and direct immunofluorescence.
Demirkesen C. Curr Opin Rheumatol 2017 - Review. PMID 27787337
Single-organ cutaneous small vessel vasculitis is a more restricted entity than hypersensitivity vasculitis and HSP. Because cutaneous polyarteritis nodosa and macular lymphocytic arteritis share some clinicopathologic features, the question is raised whether they are not two different entities. Several histopathological features defining IgG4-related disease are found in granuloma faciale and erythema elevatum diutinum, two localized chronic cutaneous vasculitis; however, in a recent series no diagnostic criteria for IgG4-related disease was detected in them. ...
Single-organ cutaneous small vessel vasculitis is a more restricted entity than hypersensitivity vasculitis and HSP. Because c …
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