Results 121 to 130 of about 1,292 (153)
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Management of Epidermolysis Bullosa Acquisita

Dermatologic Clinics, 2011
Epidermolysis bullosa acquisita is a rare and debilitating autoimmune mucocutaneous blistering disease caused by autoantibodies directed against type VII collagen or anchoring fibrils in the subepidermal basement membrane zone. Treatment is quite challenging because this disease can be recalcitrant to multiple modalities.
Lizbeth R A, Intong, Dédée F, Murrell
exaly   +3 more sources

Epidermolysis Bullosa Acquisita in Childhood

The Journal of Dermatology, 2003
AbstractEpidermolysis 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
openaire   +2 more sources

Epidermolysis Bullosa Acquisita

Archives of Dermatology, 1986
Diseases,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 ...
openaire   +2 more sources

Epidermolysis bullosa acquisita.

Archives of dermatology, 1981
Application 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 ...
H H, Roenigk, R W, Pearson
openaire   +3 more sources

EPIDERMOLYSIS BULLOSA ACQUISITA

Archives of Dermatology and Syphilology, 1934
The following case is reported in the hope that the therapy found effective in it, at any rate temporarily, may be tried by others not only in the acquired but also in the hereditary type of epidermolysis bullosa. REPORT OF A CASE T. F. C., a white man, aged 58, a stationary engine fireman, was referred to me with a chronic, distressing and ...
openaire   +1 more source

Epidermolysis Bullosa Acquisita

Archives of Dermatology, 1990
Robert A. Briggaman   +2 more
openaire   +2 more sources

Epidermolysis bullosa (acquisita).

Archives of dermatology and syphilology, 2011
E A, OLIVER, A, GREENBERG
openaire   +3 more sources

Pediatric epidermolysis bullosa acquisita: A review

Pediatric Dermatology, 2021
Naveed Sami
exaly  

Epidermolysis bullosa acquisita: Autoimmunity to anchoring fibril collagen

Autoimmunity, 2012
Mei Chen, Gene H Kim, David T Woodley
exaly  

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