Results 51 to 60 of about 23,997 (201)

Epidermolysis bullosa acquisita

Dermatology Online Journal, 2007
A 29-year-old woman presented with 8 months of multiple vesicles, erosions, and milia on the dorsa of her hands and feet. Histopathologic examination demonstrated a subepidermal blister, with a paucity of eosinophils and a lack of blood vessel wall thickening or caterpillar bodies.
Stein, Jennifer A, Mikkilineni, Radha
  +8 more sources

C5aR2 deficiency ameliorates inflammation in murine epidermolysis bullosa acquisita by regulating FcγRIIb expression on neutrophils.

Journal of Investigative Dermatology, 2022
Epidermolysis bullosa acquisita (EBA) is a rare blistering skin disease induced by autoantibodies directed against type VII collagen (COL7). Transfer of antibodies against murine COL7 (mCOL7) into mice mimics the effector phase of EBA and results in a ...
D. Seiler, Marie Kleingarn, Katja H. Kähler, Caroline Gruner, Jovan Schanzenbacher, Elvira Ehlers-Jeske, Samyr Kenno, C. Sadik, E. Schmidt, K. Bieber, J. Köhl, R. Ludwig, C. Karsten   +12 more
semanticscholar   +1 more source

Epidermolysis bullosa acquisita

Clinics in Dermatology, 2012
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) structures, a major component of anchoring fibrils, which attach the epidermis to the dermis.
Rishu, Gupta, David T, Woodley, Mei, Chen   +2 more
openaire   +3 more sources

Epidermolysis Bullosa in Calves in the United Kingdom [PDF]

, 2010
Epidermolysis bullosa (EB) was diagnosed in eight calves from four farms in the United Kingdom on the basis of clinical, histological and ultrastructural findings. In three affected herds, pedigree Simmental bulls had been mated with Simmental-cross cows.
Skuse, A.M., Philbey, A W, Higgins, R J, Fraser, M., Thompson, H., Higgins, R.J., Day, M J, Foster, A.P., Higgins, R. J., Fraser, M.A., Day, M.J., Philbey, A. W., Thomson, J., Skuse, A M, Fraser, M A, Philbey, A., Foster, A P, Bowden, P E, Bowden, P.E., Barrett, D. C., Thomson, J. R., Bowden, P. E., Fraser, Mary, Day, M. J., Thomson, J R, Thompson, H, Barrett, D C, Fraser, M. A., Barrett, D.C., Skuse, A. M., Bowden, Paul Edward, Foster, A. P.   +31 more
core   +1 more source

Epidermolysis bullosa acquisita following skin graft in donor and graft sites: A case report

Burns Open, 2023
Epidermolysis bullosa acquisita is a rare mucocutaneous autoimmune blistering disorder which usually presents in adulthood. The disease is mediated by antibodies against type VII collagen, though the precise inciting factors for autoantibody formation ...
Joyce Xia, Alice J. Tan, Gunnlaugur P. Nielsen, Ruth K. Foreman, Mai Hoang, Sean A. Hickey, Daniela Kroshinsky   +6 more
doaj   +1 more source

Epidermolysis bullosa acquisita

Indian Journal of Dermatology, Venereology and Leprology, 2006
A 20 year old male started developing bubae following even minor trauma on the skin as well as the mucous membranes during the preceding 5 years. The bunae healed with atrophic scars. Involvement of the oral mucous membrane and the eyes, scpcially the right eye, was quite extensive and unusual.
Jayanta Kr, Das, Sujata, Sengupta, Asok Kr, Gangopadhyay   +2 more
openaire   +2 more sources

Therapeutic Effect of a Novel Phosphatidylinositol-3-Kinase δ Inhibitor in Experimental Epidermolysis Bullosa Acquisita [PDF]

Frontiers in Immunology, 2018
Hiroshi Koga, Ralf Ludwig, Katja Bieber   +2 more
exaly   +2 more sources

COVID 19 and autoimmune blistering diseases: is there a link between epidermolysis bullosa acquisita and SARS-CoV-2?

, 2022
The blistering disease Epidermolysis bullosa acquisita is a genetic/autoimmune disorder derivingfrom alterations of the human protein Collagen alpha-1(VII) chain (CO7A1).
Petruzzi, M., Borgia, R., Romano, A., Nardi, G.M., Grassi, R., Contaldo, M., Serpico, R.   +6 more
core   +3 more sources

Differentiating antiepiligrin cicatricial pemphigoid from epidermolysis bullosa acquisita by indirect immunofluorescence of skin substrates lacking Type VII collagen or laminin 332: a case report and review of literature

Dermatologica Sinica, 2011
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.
Chih-Pin Chen, Richard Plunkett, Raminder Grover, Song-Jen Hong   +3 more
doaj   +1 more source

Inhibition of glucose metabolism abrogates the effector phase of bullous pemphigoid-like epidermolysis bullosa acquisita.

Journal of Investigative Dermatology, 2021
Bullous pemphigoid-like epidermolysis bullosa acquisita (EBA) is an autoantibody-driven, granulocyte-mediated skin disease. The role of cellular metabolism and its potential as therapeutic target in EBA are unknown.
P. Schilf, M. Schmitz, Aleksandra Derenda-Hell, Markus Thieme, Tabea Bremer, M. Väth, D. Zillikens, C. Sadik   +7 more
semanticscholar   +1 more source