Epidermolysis bullosa acquisita (EBA) is a rare, acquired, chronic subepidermal bullous
disease of the skin and mucosa characterized by autoantibodies to type VII collagen (C7) …

Introduction: Epidermolysis bullosa acquisita (EBA) is a rare autoimmune blistering disease
of skin and mucous membranes. EBA is caused by autoantibodies against type VII collagen …

Background Epidermolysis bullosa acquisita (EBA) is an orphan autoimmune disease.
Several clinical phenotypes have been described, but subepidermal blistering is …

Background Bullous systemic lupus erythematosus (BSLE) is a rare blistering condition
associated with systemic lupus erythematosus (SLE). Patients and methods We conducted a …

Background Epidermolysis bullosa acquisita (EBA) is a complex autoimmune bullous
disease disease with variable clinical presentations and multiple possible diagnostic tests …

Background: In major depressive disorder (MDD), findings include hyperstable regulation of
brain arousal measured by electroencephalography (EEG) vigilance analysis and …

Type VII collagen is an adhesion molecule of the extracellular matrix in epithelial basement
membranes, and the main constituent of anchoring fibrils at the dermal–epidermal junction …

BACKGROUND: Epidermolysis bullosa acquisita (EBA) is a severe autoimmune
subepidermal blistering disease characterized by autoantibodies against the N-terminal …

Epidermolysis bullosa acquisita (EBA) is a rare and acquired autoimmune subepidermal
bullous disease of skin and mucosa. EBA includes various distinct clinical manifestations …

Anchoring fibrils are adhesive suprastructures that ensure the connection of the epidermal
basement membrane with the dermal extracellular matrix. The fibrils represent polymers of …