Results 181 to 190 of about 220,566 (226)

IgA Vasculitis and IgA Nephropathy: Two Sides of the Same Coin?

Seminars in Nephrology
IgA vasculitis (IgAV) is considered a systemic form of IgA nephropathy (IgAN). The two diseases share similar geographic and ethnic distribution, along with common variants in genetic association studies.
É. Pillebout
semanticscholar   +1 more source

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

Kidney injury and colocalization of complement C3, IgA, and IgG in glomerular immune-complex deposits of patients with IgA nephropathy or IgA vasculitis with nephritis

Kidney International
Introduction: IgA nephropathy (IgAN) and IgA vasculitis-with-nephritis (IgAVN) are considered similar diseases with different spectra of clinical manifestations.
Lea Novak, S. Hall, Gary Cutter, Graham Gurganus, Dana V. Rizk, Bruce A. Julian, Mark Haas, Jan Novak   +7 more
semanticscholar   +1 more source

Histologic and Clinical Factors Associated with Kidney Outcomes in IgA Vasculitis Nephritis

American Society of Nephrology. Clinical Journal
Visual Abstract Background Nephritis is a common manifestation of IgA vasculitis and is morphologically indistinguishable from IgA nephropathy. While MEST-C scores are predictive of kidney outcomes in IgA nephropathy, their value in IgA vasculitis ...
Sean J. Barbour, Rosanna Coppo, Lee Er, É. Pillebout, Maria Luisa Russo, Charles E. Alpers, A. Fogo, Franco Ferrario, J. C. Jennette, Ian S D Roberts, H. T. Cook, Jie Ding, B. Su, Xuhui Zhong, F. Fervenza, L. Zand, L. Peruzzi, L. Lucchetti, R. Katafuchi, Yuko Shima, Norishige Yoshikawa, D. Ichikawa, Yusuke Suzuki, L. Murer, Robert J. Wyatt, Catherine Park, Raoul D. Nelson, JoAnn H. Narus, S. Wenderfer, Duvuru Geetha, E. Daugas, Renato C. Monteiro, S. Nakatani, A. Mastrangelo, M. Nuutinen, Mikael Koskela, Lutz T. Weber, Á. Hackl, Martin Pohl, C. Pecoraro, N. Tsuboi, Takashi Yokoo, I. Takafumi, Shouichi Fujimoto, G. Conti, Domenico Santoro, M. Materassi, Hong Zhang, S. Shi, Zhihong Liu, Vladimír Tesař, D. Maixnerova, C. Avila-Casado, Ingeborg M. Bajema, A. Barreca, Jan U. Becker, Jessica M. Comstock, Virgilius Cornea, Karen W. Eldin, L. Hernandez, Jean Hou, Kensuke Joh, Mercury Y. Lin, Nidia Messias, A. O. Muda, F. Pagni, F. Diomedi-Camassei, H. Tokola, M. D’Armiento, M. Seidl, Avi Rosenberg, A. Sannier, Maria Fernanda Soares, Suxia Wang, C. Zeng, Mark Haas   +75 more
semanticscholar   +1 more source

Outcome of immunosuppression in children with IgA vasculitis-related nephritis.

Nephrology, Dialysis and Transplantation
BACKGROUND AND HYPOTHESIS IgA vasculitis with nephritis (IgAVN) is the most common vasculitis in children. Treatment recommendations are, due to a lack of evidence, based on expert opinion resulting in variation.
K. Rohner, M. Marlais, Y. Ahn, Alaa Ali, Abrar Alsharief, Ana Novak, Marta Brambilla, E. Çakıcı, C. Candan, N. Canpolat, E. Yu-Hin Chan, S. Decramer, Madeleine S. Didsbury, Filipa Durão, A. Durkan, A. Düzova, Thomas A Forbes, V. Gracchi, T. Güngör, T. Horinouchi, B. Demir, Yasuko Kobayashi, Mikael Koskela, E. Kurt-Sukur, Claudio La Scola, Dean Langan, Xiaozhong Li, G. Malgieri, A. Mastrangelo, Jeesu Min, M. Mizerska-Wasiak, N. Moussaoui, A. Noyan, M. Nuutinen, Jennifer O'Gormon, T. Okamoto, L. Oni, M. Oosterveld, Małgorzata Pańczyk-Tomaszewska, G. Parmaksiz, Andrea Pasini, P. Rianthavorn, J. Roelofs, Yunyan Shen, R. Sinha, R. Topaloğlu, D. Torres, T. Udagawa, M. Wennerström, Y. Yap, K. Tullus   +50 more
semanticscholar   +1 more source

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 nephritis-outcomes in adult-onset disease.

Rheumatology
OBJECTIVES IgA vasculitis (IgAV) in adults has been relatively under-investigated. Since outcomes are worse in other forms of vasculitis with increasing age, we investigated the outcomes of IgAV comparing younger adults (18-34), middle aged adults (35-64)
James Stanway, Nina Brown, Afeera Pervez, E. Van de Perre, J. Tollitt, Nikolaos Marketos, Nikki L Wong, A. Dhaygude, A. Ponnusamy, E. O'Riordan, M. Venning, M. Segelmark, M. Morgan, D. Jayne, Patrick Hamilton, C. Pusey, Louise Oni, Alan D. Salama   +17 more
semanticscholar   +1 more source

Clinical and histological comparison of IgA nephritis and renal IgA vasculitis.

Nephrology, Dialysis and Transplantation
BACKGROUND IgA nephritis (IgAN) and renal IgA vasculitis (IgAV) show renal IgA deposits, but whether these two diseases are distinct entities or a spectrum of the same condition is under debate.
J. Friedrich, Maren Bellmann, D. Klank, S. Porubský, Raoul Bergner   +4 more
semanticscholar   +1 more source

IgA Vasculitis

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