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1945 8
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1949 41
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1952 36
1953 32
1954 31
1955 45
1956 44
1957 56
1958 49
1959 35
1960 36
1961 29
1962 23
1963 30
1964 32
1965 10
1968 1
1970 2
1971 1
1973 8
1974 7
1975 30
1976 55
1977 58
1978 49
1979 42
1980 56
1981 48
1982 55
1983 82
1984 63
1985 76
1986 71
1987 86
1988 73
1989 65
1990 83
1991 66
1992 96
1993 80
1994 103
1995 78
1996 92
1997 107
1998 117
1999 100
2000 120
2001 112
2002 120
2003 110
2004 137
2005 135
2006 146
2007 181
2008 161
2009 140
2010 136
2011 153
2012 146
2013 137
2014 136
2015 147
2016 151
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6,505 results

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Page 1
European consensus-based recommendations for diagnosis and treatment of immunoglobulin A vasculitis-the SHARE initiative.
Ozen S, Marks SD, Brogan P, Groot N, de Graeff N, Avcin T, Bader-Meunier B, Dolezalova P, Feldman BM, Kone-Paut I, Lahdenne P, McCann L, Pilkington C, Ravelli A, van Royen A, Uziel Y, Vastert B, Wulffraat N, Kamphuis S, Beresford MW. Ozen S, et al. Rheumatology (Oxford). 2019 Sep 1;58(9):1607-1616. doi: 10.1093/rheumatology/kez041. Rheumatology (Oxford). 2019. PMID: 30879080
OBJECTIVES: IgA vasculitis (IgAV, formerly known as Henoch-Schonlein purpura) is the most common cause of systemic vasculitis in childhood. ...
OBJECTIVES: IgA vasculitis (IgAV, formerly known as Henoch-Schonlein purpura) is the most common cause of systemic vasculit …
[Update on immunoglobulin A vasculitis].
Neumann T. Neumann T. Z Rheumatol. 2022 May;81(4):305-312. doi: 10.1007/s00393-022-01162-z. Epub 2022 Mar 18. Z Rheumatol. 2022. PMID: 35303751 Free PMC article. Review. German.
Immunoglobulin A vasculitis (IgAV) is a systemic vasculitis of the small vessels with formation of IgA immune complexes and a broad spectrum of clinical constellations. Typical manifestations include purpura, arthralgia or arthritis, enteritis a …
Immunoglobulin A vasculitis (IgAV) is a systemic vasculitis of the small vessels with formation of IgA im …
Immunoglobulin A vasculitis: The clinical features and pathophysiology.
Hu YC, Yang YH, Chiang BL. Hu YC, et al. Kaohsiung J Med Sci. 2024 Jul;40(7):612-620. doi: 10.1002/kjm2.12852. Epub 2024 Jun 3. Kaohsiung J Med Sci. 2024. PMID: 38828518 Free PMC article. Review.
Palpable purpura, gastrointestinal symptoms, joint involvement, and renal disease characterize immunoglobulin A vasculitis (IgAV). Renal involvement ranging from mild proteinuria to severe nephritic or nephrotic syndrome highlights the importance of monitorin …
Palpable purpura, gastrointestinal symptoms, joint involvement, and renal disease characterize immunoglobulin A vasculitis …
[Immunoglobulin A vasculitis].
Adler S. Adler S. Inn Med (Heidelb). 2024 Feb;65(2):114-121. doi: 10.1007/s00108-023-01650-7. Epub 2024 Jan 18. Inn Med (Heidelb). 2024. PMID: 38236411 Review. German.
In adults, immunoglobulin A (IgA) vasculitis often proceeds more severely und recurrently with the classical tetrad of skin manifestations in the sense of leukocytoclastic vasculitis, joint affection, gastrointestinal involvement and IgA nephritis, in …
In adults, immunoglobulin A (IgA) vasculitis often proceeds more severely und recurrently with the classical tetrad of skin ma …
Immunoglobulin A Vasculitis With Intussusception in Children.
Liu C, Du LN, Zhao Q, Wang XT, Feng K, Yang Y, Yang Y. Liu C, et al. Am Surg. 2024 Jun;90(6):1298-1308. doi: 10.1177/00031348241229627. Epub 2024 Jan 24. Am Surg. 2024. PMID: 38264960 Review.
BACKGROUND: Immunoglobulin A (IgA) vasculitis with intussusception is acute and severe vasculitis combined with acute abdomen in children. ...
BACKGROUND: Immunoglobulin A (IgA) vasculitis with intussusception is acute and severe vasculitis combined with acute a …
Pathogenesis of IgA Vasculitis: An Up-To-Date Review.
Song Y, Huang X, Yu G, Qiao J, Cheng J, Wu J, Chen J. Song Y, et al. Front Immunol. 2021 Nov 9;12:771619. doi: 10.3389/fimmu.2021.771619. eCollection 2021. Front Immunol. 2021. PMID: 34858429 Free PMC article. Review.
Immunoglobin A (IgA) vasculitis (IgAV), formerly called the Henoch-Schonlein purpura (HSP), is a small vessel vasculitis, characterized by IgA1-dominant immune deposition at diseased vessel walls. IgAV is the most common form of vasculitis in children; …
Immunoglobin A (IgA) vasculitis (IgAV), formerly called the Henoch-Schonlein purpura (HSP), is a small vessel vasculitis …
[Immunoglobulin A vasculitis (IgAV)].
Rose K, Turner JE, Iking-Konert C. Rose K, et al. Z Rheumatol. 2023 Sep;82(7):587-598. doi: 10.1007/s00393-023-01355-0. Epub 2023 Jun 2. Z Rheumatol. 2023. PMID: 37266676 Free PMC article. German.
IgA vasculitis (IgAV) is an immune complex-mediated vasculitis characterized by IgA1-dominant immune deposits in small vessels. ...Management of renal and gastrointestinal manifestations follows recommendations for ANCA-associated vasculitis and IgA …
IgA vasculitis (IgAV) is an immune complex-mediated vasculitis characterized by IgA1-dominant immune deposits in small …
Penile involvement of immunoglobulin a vasculitis/Henoch-Schonlein purpura.
Kaya Akca U, Batu ED, Serin O, Ipek OF, Aydin O, Teksam O, Bilginer Y, Ozen S. Kaya Akca U, et al. J Pediatr Urol. 2021 Jun;17(3):409.e1-409.e8. doi: 10.1016/j.jpurol.2021.01.012. Epub 2021 Jan 22. J Pediatr Urol. 2021. PMID: 33558175 Review.
BACKGROUND: Immunoglobulin A vasculitis/Henoch-Schonlein purpura (IgAV/HSP) is a leukocytoclasia vasculitis of childhood, predominantly affecting the skin, joints, gastrointestinal tract, and kidneys. ...
BACKGROUND: Immunoglobulin A vasculitis/Henoch-Schonlein purpura (IgAV/HSP) is a leukocytoclasia vasculitis of c …
6,505 results