Coexistence of anti-glomerular basement membrane disease and IgA nephropathy: an illustrative case and comprehensive literature review
Author:
Affiliation:
1. Kidney Institute, Department of Nephrology, Shanghai Changzheng Hospital, Naval Military Medical University, Shanghai, China
2. Department of Nephrology, The First Navy Hospital of Southern Theater Command, Zhanjiang, China
Funder
the Clinical Research Project of Shanghai Municipal Health Commission
the Science and Technology Innovation Plan of Shanghai Science and Technology Commission
the National Natural Science Foundation of China
Publisher
Informa UK Limited
Link
https://www.tandfonline.com/doi/pdf/10.1080/0886022X.2024.2323160
Reference53 articles.
1. Atypical Anti-Glomerular Basement Membrane Disease
2. Anti-glomerular Basement Membrane Disease After Diagnosis of Immunoglobulin A Nephropathy: A Case Report
3. The immunoglobulin G subclass distribution of anti-GBM autoantibodies against rHα3(IV)NC1 is associated with disease severity
4. Recurrent Goodpasture’s disease secondary to a monoclonal IgA1-κ antibody autoreactive with the α1/α2 chains of type IV collagen
5. Increased Goodpasture Antigen-Binding Protein Expression Induces Type IV Collagen Disorganization and Deposit of Immunoglobulin A in Glomerular Basement Membrane
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