Results 141 to 150 of about 15,099 (182)

Multisystemic manifestations of IgA vasculitis

Clinical Rheumatology, 2020
Immunoglobulin A vasculitis (IgAV), also known as Henoch-Schönlein Purpura, is one of the most common kind of systemic vasculitis in children, and due to the involvement of small blood vessels throughout the body, this disease can cause a variety of symptoms in different organs. Our aim was to review the data on various systemic manifestations of IgAV.
Lina Du, Panpan Wang, Chang Liu, Shaojing Li, Shuang Yue, Yan Yang   +5 more
openaire   +2 more sources

IgA vasculitis with severe renal manifestation

BMJ Case Reports, 2022
IgA vasculitis is a rare systemic vasculitis in adults, frequently more severe than in paediatric age. It manifests with cutaneous, articular, gastrointestinal and renal involvement. We present a case of a man in his 40s diagnosed with IgA vasculitis with cutaneous, joint, gastrointestinal and renal disease.
Joana, Marques Dias, Marta Azevedo, Ferreira, Ana, Grilo, Fernando Martos, Gonçalves   +3 more
openaire   +2 more sources

Serum levels of galactose-deficient IgA1 in Chinese children with IgA nephropathy, IgA vasculitis with nephritis, and IgA vasculitis

Clinical and Experimental Nephrology, 2020
IgA nephropathy (IgAN) and IgA vasculitis with nephritis (IgAV-N) are related diseases. Galactose-deficient IgA1 (Gd-IgA1) plays an important role in the pathology of IgAV-N and IgAN, so we aim to compare the serum levels of Gd-IgA1 in Chinese pediatric patients with IgAN, IgAV-N, and IgAV.We retrospectively enrolled 52 patients with IgAN, 57 patients ...
Mengmeng, Tang, Xue, Zhang, Xueqian, Li, Lei, Lei, Hejia, Zhang, Chen, Ling, Jie, Ni, Jicheng, Lv, Xiaorong, Liu, Xiangmei, Chen   +9 more
openaire   +2 more sources

IgA Vasculitis

Journal of General Internal Medicine, 2022
Natalie Garcia, Victoria Jiminez, Alonso Heudebert   +2 more
openaire   +2 more sources

IgA vasculitis

QJM: An International Journal of Medicine, 2023
T, Tadokoro, T, Abe, T, Nakano, Y, Kimura, K, Higaki, S, Hayashidani, H, Tashiro   +6 more
openaire   +2 more sources

IgA Vasculitis in Adults

Current Treatment Options in Rheumatology, 2018
Immunoglobulin A vasculitis (IgAV) is a small vessel vasculitis with skin, joint, gastrointestinal and renal manifestations. Our understanding of the natural history of this disease is limited due to the overall low incidence of IgAV in adults and a lack of consensus regarding diagnostic criteria.
Sarah M. Moran, Heather N. Reich
openaire   +1 more source

IgA nephropathy: A vasculitis?

Nephrology, 1997
Summary: Vasculitis is an inflammation of blood vessels which leads to necrosis and infarction of the endorgans involved. IgA nephropathy (IgAN) is the kidney‐limited expression of a single disease with Henoch‐Schonlei purpura as the systemic vasculitic form.
openaire   +1 more source

COVID-19 and IgA Vasculitis

The Journal of Rheumatology, 2022
Rujittika Mungmunpuntipantip, Viroj Wiwanitkit   +1 more
openaire   +2 more sources

IgA Nephropathy and IgA Vasculitis

2022
Haresh Selvaskandan, Chee Kay Cheung, Jonathan Barratt   +2 more
openaire   +1 more source

[IgA vasculitis - similarities and differences to IgA nephropathy].

Therapeutische Umschau. Revue therapeutique, 2022
IgA vasculitis - similarities and differences to IgA nephropathy Abstract. IgA vasculitis (IgAV), formerly called Henoch-Schönlein Purpura (HSP) is an immune complex-mediated vasculitis of small vessels typically affecting the skin, gastrointestinal tract, and the kidneys. Based on distinct histopathological and pathophysiological commonalities of IgAV
openaire   +1 more source