Bullous Pemphigoid With a Dual Pattern of Glomerular Immune Complex Disease
Author:
Publisher
Elsevier BV
Subject
Nephrology
Reference14 articles.
1. Diagnosis and classification of autoimmune blistering diseases;Baum;Autoimmun Rev,2014
2. Human IgG1 monoclonal antibody against human collagen 17 noncollagenous 16A domain induces blisters via complement activation in experimental bullous pemphigoid model;Li;J Immunol,2010
3. Evaluation of a BP180-NC16a enzyme-linked immunosorbent assay in the initial diagnosis of bullous pemphigoid;Sakuma-Oyama;Br J Dermatol,2004
4. Update on the pathogenesis of bullous pemphigoid: an autoantibody-mediated blistering disease targeting collagen XVII;Nishie;J Dermatol Sci,2014
5. Anti-glomerular basement membrane nephritis and bullous pemphigoid caused by distinct anti-alpha 3(IV)NC1 and anti-BP180 antibodies in a patient with Crohn's disease;Plaisier;Am J Kidney Dis,2002
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2. The relationship between bullous pemphigoid and renal disease and related treatments: a review of the current literature;Expert Review of Clinical Immunology;2023-09-14
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4. A Case of Severe and Refractory Membranous Nephropathy Associated to Mucous Membrane Pemphigoid;Case Reports in Nephrology;2021-05-11
5. Concurrent mucous membrane pemphigoid and membranous glomerulonephritis in a patient with autoantibodies targeting the 1080 region of collagen XVII;British Journal of Dermatology;2019-07-15
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