Epidermolysis Bullosa Acquisita (Brunsting-Perry Pemphigoid Variant) Localized to the Face and Diagnosed With Antigen Identification Using Skin Deficient in Type VII Collagen-Reference-Cited by-同舟云学术

Epidermolysis Bullosa Acquisita (Brunsting-Perry Pemphigoid Variant) Localized to the Face and Diagnosed With Antigen Identification Using Skin Deficient in Type VII Collagen

Published:2017-07 Issue:7 Volume:39 Page:e90-e96
ISSN:0193-1091
Container-title:The American Journal of Dermatopathology
language:en
Short-container-title:

Author:

Asfour Leila,Chong Heung,Mee John,Groves Richard,Singh Manuraj

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Dermatology,General Medicine,Pathology and Forensic Medicine

Reference42 articles.

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2. Epidermolysis bullosa acquisita: autoimmunity to anchoring fibril collagen;Chen;Autoimmunity,2012

3. Epidermolysis bullosa acquisita presenting with localized facial blisters;Lee;Clin Exp Dermatol.,1992

4. A case of epidermolysis bullosa acquisita with clinical features of Brunsting–Perry pemphigoid showing an excellent response to colchicine;Tanaka;J Am Acad Dermatol.,2009

5. Epidermolysis bullosa acquisita—a pemphigoid like disease;Gammon;J Am Acad Dermatol.,1984

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