CP Chen, R Plunkett, R Grover… - Dermatologica Sinica, 2011 - Elsevier Antiepiligrin cicatricial pemphigoid (AECP) is a chronic autoimmune subepidermal blistering disease characterized by clinical features of cicatricial pemphigoid and circulating IgG antibasement membrane autoantibodies directed against laminin 332. There is growing evidence of an ... All 2 versions
ML Abrams, A Smidt, L Benjamin… - Archives of …, 2011 - Am Med Assoc Background Epidermolysis bullosa acquisita (EBA) is a rare, chronic, autoimmune bullous dermatosis that is caused by autoantibodies against the noncollagenous terminus of the α chain of type VII collagen, resulting in decreased anchoring fibrils in the lamina densa. It classically ... Cited by 1 - Related articles - All 4 versions
F Caux - Dermatologic clinics, 2011 - ncbi.nlm.nih.gov Epidermolysis bullosa acquisita (EBA) is a rare autoimmune subepidermal blistering disease characterized by immune deposits on anchoring fibrils of cutaneous and mucosal basement membrane zones. It is due to circulating antibodies directed to type VII collagen. Clinical ... Cited by 1 - All 2 versions
MA Saleh, K Ishii, YJ Kim, A Murakami… - Journal of …, 2011 - Elsevier Epidermolysis bullosa acquisita (EBA) is an acquired autoimmune mechanobullous disease. EBA patients possess autoantibodies against type VII collagen which is composed of a collagenous domain flanked by non-collagenous NC1 and NC2 domains. It was ... All 3 versions
[HTML] from nih.govJ Tu… - Indian Journal of Dermatology, 2011 - ncbi.nlm.nih.gov Your browser version may not work well with NCBI's web applications. More information here... ... From the Department of Dermatology, Sir Charles Gairdner Hospital, Nedlands, Western Australia 6009, Australia. ... 1 Consultant Dermatologist, Royal Perth Hospital and St ... Related articles - All 4 versions