Yahoo Poland Wyszukiwanie w Internecie

Search results

  1. 27 lut 2023 · Epidermolysis bullosa acquisita is the second most common AISBD of dogs (26% of all AISBDs) . Most affected dogs are young (median: 1.2 years; range: 4 months – 8 years) males (M:F ratio = 2.3), with almost half of them (45%) developing lesions before 1 year of age [ 30 ].

  2. 15 wrz 2015 · Epidermolysis bullosa acquisita (EBA) is a rare autoimmune subepidermal blistering disease of dogs and humans. Objectives. Our objectives were to describe clinical phenotypes, histopathology and treatment outcomes of canine EBA. Animals. Twenty dogs diagnosed with EBA based on a subepidermal blister formation and collagen VII autoreactivity ...

  3. 30 paź 2014 · Epidermolysis bullosa (EB) is a hereditary mechanobullous disease of animals and humans, characterized by an extreme fragility of the skin and mucous membranes. The main feature of EB in humans and animals is the formation of blisters and erosions in response to minor mechanical trauma.

  4. 15 wrz 2015 · Background: Epidermolysis bullosa acquisita (EBA) is a rare autoimmune subepidermal blistering disease of dogs and humans. Objectives: Our objectives were to describe clinical phenotypes,...

  5. Epidermolysis bullosa (EB) is a hereditary mechanobullous disease of animals and humans, characterized by an extreme fragility of the skin and mucous membranes. The main feature of EB in humans and animals is the formation of blisters and erosions in response to minor mechanical trauma.

  6. 29 gru 2003 · Epidermolysis bullosa acquisita (EBA) is an AISBD characterized by the production of autoantibodies against collagen VII in sublamina densa anchoring fibrils.

  7. 1 lut 2023 · Epidermolysis bullosa acquisita (EBA) is a rare chronic autoimmune subepidermal blistering disease of the skin and mucous membranes, usually beginning in adulthood. EBA is induced by autoantibodies to type VII collagen, a major component of anchoring fibrils in the dermal–epidermal junction (DEJ).