Epidermolysis bullosa acquisita (EBA) is an orphan autoimmune disease. Patients with EBA
suffer from chronic inflammation as well as blistering and scarring of the skin and mucous …

Autoimmune skin blistering diseases (AIBD) are characterized by autoantibodies that are
directed against structural proteins in the skin and adjacent mucous membranes. Some …

Recessive dystrophic epidermolysis bullosa (RDEB) is a lifelong genodermatosis
associated with blistering, wounding, and scarring caused by mutations in COL7A1, the …

Autoimmune bullous disorders (AIBDs) are a heterogeneous group of rare diseases
clinically characterized by erosions and/or blisters on the skin and mucous membranes …

• Introduction• Pemphigus diseases‐Pemphigus vulgaris‐Pemphigus foliaceus• Pemphigus
variants‐Pemphigus herpetiformis‐Pemphigus erythematosus‐Drug‐induced pemphigus …

Autoimmune bullous dermatoses (AIBD) encompass a variety of organ-specific autoimmune
diseases that manifest with cutaneous and/or mucosal blisters and erosions. They are …

Epidermolysis bullosa acquisita (EBA) is a chronic mucocutaneous autoimmune skin
blistering disease. The pathogenic relevance of autoantibodies targeting type VII collagen …

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 …

The pemphigoid group is a category of autoimmune subepidermal blistering diseases in
which autoantibodies deposit linearly at the epidermal basement membrane zone (BMZ) …