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Epidermolysis bullosa acquisita
Der Hautarzt, 2019Epidermolysis bullosa acquisita (EBA) is a rare acquired subepidermal bullous autoimmune dermatosis, associated with autoantibodies against collagen type VII, the most important component of dermal anchoring fibrils. Blister induction occurs after binding of autoantibodies to collagen type VII, leading to complement activation, recruitment of ...
S C, Hofmann, A, Weidinger
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Matrix Biology, 2018
Epidermolysis bullosa (EB), a group of heritable skin fragility disorders, is characterized by blistering, erosions and chronic ulcers in the skin and mucous membranes.
C. Has +4 more
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Epidermolysis bullosa (EB), a group of heritable skin fragility disorders, is characterized by blistering, erosions and chronic ulcers in the skin and mucous membranes.
C. Has +4 more
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Investigational Treatments for Epidermolysis Bullosa
American Journal of Clinical Dermatology, 2021P. Hou +5 more
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Hereditary Epidermolysis Bullosa
Archives of Dermatology, 1967Case reports, with histochemical and biochemical studies of biopsy material, are presented of epidermolysis bullosa simplex (EBS), an epidermal disease with cleavage through the basal cell layer; epidermolysis bullosa dystrophic dominant (EBDD), a junctional disease with cleavage through the PAS-positive membrane; and epidermolysis bullosa dystrophic ...
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Dystrophic Epidermolysis Bullosa
Clinical Pediatrics, 1981The three forms of dystrophic epidermolysis bullosa include the autosomal recessive form and two autosomal dominant variants, the Cockayne-Touraine and Pasini forms. Whereas all three forms are clinically characterized by milia, nail dystrophy, and scarring, the autosomal recessive form tends to be the most mutilating .with frequent mucosal lesions ...
C G, Burkhart, E S, Ruppert
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Dermatologic Clinics, 2010
The prevalence of epidermolysis bullosa simplex (EBS) is estimated to be approximately 6 to 30 per 1 million live births. The disease is usually caused by missense mutations in KRT5 and KRT14, encoding keratins mostly expressed in the epidermal basal layer.
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The prevalence of epidermolysis bullosa simplex (EBS) is estimated to be approximately 6 to 30 per 1 million live births. The disease is usually caused by missense mutations in KRT5 and KRT14, encoding keratins mostly expressed in the epidermal basal layer.
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