Autoimmune subepidermal blistering diseases of the skin and mucosae constitute a large
group of sometimes devastating diseases, encompassing bullous pemphigoid, gestational …

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

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

Autoimmune bullous diseases are a group of chronic inflammatory disorders caused by
autoantibodies targeted against structural proteins of the desmosomal and …

The dermal‐epidermal junction consists of a network of several interacting structural
proteins that strengthen adhesion and mediate signalling events. This structural network …

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 …

Subepidermal autoimmune bullous diseases of the skin and mucosae comprise a large
group of chronic diseases, including bullous pemphigoid, pemphigoid gestationis, mucous …

Autoimmune bullous skin diseases, such as pemphigus and pemphigoid, may enable
clarification of the mechanisms of immune regulation in the skin. Pemphigus and …

Background Autoimmune bullous diseases/dermatoses (AIBDs) are severe autoantibody-
mediated skin diseases. The pathogenic relevance of autoreactive CD4+ T cells for the …

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