Development of bullous pemphigoid in junctional epidermolysis bullosa
Author:
Affiliation:
1. First Dermatologic Division IDI‐IRCCS Rome Italy
2. Laboratory of Molecular and Cell Biology IDI‐IRCCS Rome Italy
Publisher
Wiley
Subject
Infectious Diseases,Dermatology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/jdv.16057
Reference10 articles.
1. Inherited epidermolysis bullosa: Updated recommendations on diagnosis and classification
2. Prevalence of specific anti-skin autoantibodies in a cohort of patients with inherited epidermolysis bullosa
3. De Novo Anti-Type VII Collagen Antibodies in Patients with Recessive Dystrophic Epidermolysis Bullosa
4. Proinflammatory Cytokines and Antiskin Autoantibodies in Patients With Inherited Epidermolysis Bullosa
5. Epidermolysis Bullosa (EB) Acquisita in an Adult Patient with Previously Unrecognized Mild Dystrophic EB and Biallelic COL7A1 Mutations
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1. Absence of NC14A Domain of COLXVII/BP180 in Mice Results in IL-17‒Associated Skin Inflammation;Journal of Investigative Dermatology;2023-01
2. Case report: bullous pemphigoid development underlies dystrophic epidermolysis bullosa disease worsening;Frontiers in Immunology;2022-07-29
3. Occurrence of autoantibodies against skin proteins in patients with hereditary epidermolysis bullosa predisposes to development of autoimmune blistering disease;Frontiers in Immunology;2022-07-25
4. A Review of Acquired Autoimmune Blistering Diseases in Inherited Epidermolysis Bullosa: Implications for the Future of Gene Therapy;Antibodies;2021-05-17
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