Treatment of epidermolysis bullosa acquisita with intravenous immunoglobulin in patients non-responsive to conventional therapy: clinical outcome and post-treatment long-term follow-up
Author:
Publisher
Wiley
Subject
Infectious Diseases,Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-3083.2011.04205.x/fullpdf
Reference40 articles.
1. Autoimmunity to type VII collagen: epidermolysis bullosa acquisita;Remington;Curr Dir Autoimmun,2008
2. Epidermolysis bullosa acquisita sera react with distinct epitopes on the NC1 and NC2 domains of type VII collagen: study using immunoblotting of domain-specific recombinant proteins and postembedding immunoelectron microscopy;Ishii;Br J Dermatol,2004
3. Incidence and distribution of subepidermal autoimmune bullous skin diseases in three French regions. Bullous Diseases French Study Group;Bernard;Arch Dermatol,1995
4. Development of an ELISA for rapid detection of anti-type VII collagen autoantibodies in epidermolysis bullosa acquisita;Chen;J Invest Dermatol,1997
5. Epidermolysis bullosa acquisita: concise review and practical considerations;Lehman;Int J Dermatol,2009
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1. Intravenous Immunoglobulin for Autoimmune Bullous Diseases: A Case Series from a Central European Referral Center;Medicina;2023-07-07
2. A systematic review on efficacy, safety and treatment durability of intravenous immunoglobulin in autoimmune bullous dermatoses: Special focus on indication and combination therapy;Experimental Dermatology;2023-05-07
3. Epidermolysis Bullosa Acquisita—Current and Emerging Treatments;Journal of Clinical Medicine;2023-02-01
4. Therapeutic effects of Fc gamma RIV inhibition are mediated by selectively blocking immune complex-induced neutrophil activation in epidermolysis bullosa acquisita;Frontiers in Immunology;2022-10-13
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