U-serrated immunodeposition pattern differentiates type VII collagen targeting bullous diseases from other subepidermal bullous autoimmune diseases
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2004.06006.x/fullpdf
Reference21 articles.
1. Bullous pemphigoid and epidermolysis bullosa acquisita. Differentiation by fluorescence overlay antigen mapping
2. A stepwise approach to the diagnosis of blisters in the clinic1 1Abbreviations used in this text: BP, bullous pemphigoid; DH, dermatitis herpetiformis; EB, epidermolysis bullosa; EBA, epidermolysis bullosa acquisita; EREF, endogenous reaction to environmental factor; IMF, immunofluorescence; LAD, linear IgA disease; MMP, mucous membrane pemphigoid (formerly known as cicatricial pemphigoid); PCT, porphyria cutanea tarda; PF, pemphigus foliaceous; PG, pemphigoid gestationis; PV, pemphigus vulgaris; SLE, systemic lupus erythematosus; TEN, toxic epidermal necrolysis.
3. Direct immunofluorescence microscopy in the diagnosis of autoimmune bullous dermatoses
4. Indirect immunofluorescence microscopy for the serological diagnosis of autoimmune blistering skin diseases
5. Immunoblot assay in differential diagnosis of autoimmune blistering skin diseases
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