Results 171 to 180 of about 23,997 (201)
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Colchicine for epidermolysis bullosa acquisita
Journal of the American Academy of Dermatology, 1996Epidermolysis bullosa acquisita (EBA) is a chronic subepidermal blistering disease that is difficult to treat. Recently one patient with severe EBA was described who responded dramatically to colchicine.Our purpose was to determine the efficacy of colchicine in the treatment of EBA.Four patients with severe EBA refractory to conventional therapy were ...
B B, Cunningham +2 more
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Childhood epidermolysis bullosa acquisita
British Journal of Dermatology, 1994We report a 6-year-old boy suffering from acquired epidermolysis bullosa, who presented with extensive lesions of the mucous membranes and disseminated, herpetiform and 'cluster of jewels'-like vesicles and bullae arising on erythematous plaques. Direct immunofluorescence showed linear deposits of IgG and C3 at the epidermal basement membrane zone ...
Inauen P +4 more
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Epidermolysis Bullosa Acquisita in Childhood
The Journal of Dermatology, 2003AbstractEpidermolysis bullosa acquisita (EBA) is a subepidermal autoimmune blistering disease that is rarely reported in childhood. We describe a nine‐month‐old mulatto boy presenting with multiple, annular, widespread, tense blisters and oral lesions. The diagnosis of EBA was confirmed by histopathology, immunofluorescence, and immunoblotting analysis.
Fanny X, Trigo-Guzmán +8 more
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Epidermolysis bullosa acquisita: A comprehensive review.
Autoimmunity Reviews, 2019Epidermolysis bullosa acquisita is a rare autoimmune blistering disease which results in vesicle and bullae formation on the skin and erosions on the mucous membranes. EBA is mediated by autoantibodies to collagen VII.
K. Kridin +4 more
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Epidermolysis Bullosa Acquisita
Archives of Dermatology, 1986Diseases,it seems, have lives of their own, both in the concrete terms of their natural history in an affected individual and in the abstract terms of their definition as clinical entities. As clinical entities, the criteria that are developed through observation and investigation and that are used to define specific diseases can be likened to the ...
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Epidermolysis Bullosa Acquisita
Archives of Dermatology, 1981Application of newly developed or refined laboratory techniques to a variety of diseases has often resulted in modification of time-honored clinical classifications. In the blistering diseases, the techniques of immunopathologic study and electron microscopy have provided the basis for more accurate diagnoses and more rational speculations on ...
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Epidermolysis bullosa acquisita induced by atezolizumab
Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 2023E. Carmona-Rocha +6 more
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Epidermolysis Bullosa Acquisita
Archives of Dermatology, 1990Robert A. Briggaman +2 more
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Epidermolysis Bullosa Acquisita
Archives of Dermatology, 1971Epidermolysis bullosa acquisita (EBA) is a rare, nonhereditary, blistering disease with clinical features similar to epidermolysis bullosa dystrophica. The clinical features may often simulate porphyria cutanea tarda, pemphigus, or pemphigoid. Three new cases of EBA are discussed. The first patient had signs of a "lymphoma-like" disorder of lymph nodes.
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