Results 91 to 100 of about 22,551 (179)
Epidermolysis Bullosa Acquisita Antigen: Relationship Between the Collagenase-Sensitive and -Insensitive Domains [PDF]
, 1988 To clarify the relationship of the 290 and 145kDa chains of the epidermolysis bullosa acquisita (EBA) antigen, we subjected urea extracts of skin basement membrane zone (BMZ) proteins and isolated 290 and 145kDa chains of the EBA antigen cut out of ...
Takashi. Yoshiike +5 more
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PLoS ONE, 2013 Autoantibodies are believed to be maintained by either the continuous generation of short-lived plasma cells in secondary lymphoid tissues or by long-lived plasma cells localized in bone marrow and spleen.
Benjamin Tiburzy +10 more
doaj +1 more source
Epidermolysis bullosa acquisita: a retrospective clinical analysis of 30 cases [PDF]
, 2011 Epidermolysis bullosa acquisita (EBA) is an acquired, autoimmune blistering disorder caused by autoantibody production against type VII collagen. The aim of this study was to examine the clinical types, treatments, and outcomes of 30 patients with EBA ...
김수찬, 김종훈
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A rare occurrence of epidermolysis bullosa acquisita in a patient with retroviral disease
, 2017 Epidermolysis bullosa acquisita is a chronic subepidermal blistering disease associated with autoimmunity to type-VII collagen within anchoring fibrils located at the dermo-epidermal junction. This entity is rarely reported from India.
Tambe Swagata +3 more
core +1 more source
Epidermolysis Bullosa Acquisita Antigen, a New Major Component of Cutaneous Basement Membrane, Is a Glycoprotein with Collagenous Domains [PDF]
, 1986 The epidermolysis bullosa acquisita antigen is a major constituent of the basement membrane zone beneath stratified squamous epithelium. The antigen which is recognized in extracts of skin basement membrane by Western blot analysis with polyclonal or ...
O'Keefe, Edward +5 more
core +1 more source
Frontiers in ImmunologyAutoimmune blistering skin diseases have deleterious effects on patients’ lives with a great (and unmet) need for more treatment options and potential new drug targets.
Lili Balogh +16 more
doaj +1 more source
Complement-fixing abilities and IgG subclasses of autoantibodies in epidermolysis bullosa acquisita
, 1998 Epidermolysis bullosa acquisita (EBA) is an autoimmune-mediated subepidermal bullous disease in which the target of the autoantibodies is type VII collagen, a major component of anchoring fibrils.
김수찬
core +1 more source
, 1992 The integrin alpha 6 beta 4 complex is a protein of the membrane of basal keratinocytes, localized at the surface of cells in contact with the basement membrane zone in normal skin.
E. Berti +6 more
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Successful Treatment of Localized Epidermolysis Bullosa Acquisita with Low-dose Dapsone and Topical Tacrolimus [PDF]
, 2009 A 52-year-old man had a twenty-five year history of recurrent bullous eruption that was localized to both cheeks. The diagnosis of epidermolysis bullosa acquisita was confirmed by means of direct immunofluorescence and salt-split direct ...
김수찬, 이상은
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Epidermolysis bullosa acquisita: treatment with intravenous immunoglobulins
, 2002 Epidermolysis bullosa acquisita (EBA) is a rare autoimmune bullous disorder that is often difficult to treat. Few cases have been reported and therapy consists mainly of combinations of systemic steroids, immunosuppressants and, recently, administration ...
Nicolaidou, E +6 more
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