A case of junctional epidermolysis bullosa with prurigo-like lesions and reduction of collagen XVII and filaggrin
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjd.12241/fullpdf
Reference11 articles.
1. The classification of inherited epidermolysis bullosa (EB): report of the Third International Consensus Meeting on Diagnosis and Classification of EB;Fine;J Am Acad Dermatol,2008
2. Localized and generalized forms of blistering in junctional epidermolysis bullosa due to COL17A1 mutations in the Netherlands;Pasmooij;Br J Dermatol,2007
3. Molecular mechanisms of phenotypic variability in junctional epidermolysis bullosa;Kiritsi;J Med Genet,2011
4. Dynamic interactions of epidermal collagen XVII with the extracellular matrix: laminin 332 as a major binding partner;Nishie;Am J Pathol,2011
5. Autosomal dominant junctional epidermolysis bullosa;Almaani;Br J Dermatol,2009
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1. Strategy for the Optimization of Read-Through Therapy for Junctional Epidermolysis Bullosa with COL17A1 Nonsense Mutation;Journal of Investigative Dermatology;2024-03
2. A case of junctional epidermolysis bullosa intermediate with collagen XVII deficiency treated with dupilumab;Journal of Dermatological Treatment;2023-11-15
3. Prevalence, pathophysiology and management of itch in epidermolysis bullosa*;British Journal of Dermatology;2020-11-29
4. Non–Cell-Autonomous Activity of the Hemidesmosomal Protein BP180/Collagen XVII in Granulopoiesis in Humanized NC16A Mice;The Journal of Immunology;2020-09-30
5. A Silent COL17A1 Variant Alters Splicing and Causes Junctional Epidermolysis Bullosa;Acta Dermato Venereologica;2019
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