Literature DB >> 21605802

Diagnosis and clinical features of pemphigus vulgaris.

Supriya S Venugopal1, Dédée F Murrell.   

Abstract

Autoimmune bullous diseases are associated with autoimmunity against structural components that maintain cell-cell and cell-matrix adhesion in the skin and mucous membranes. They include those where the skin blisters at the basement membrane zone and those where the skin blisters within the epidermis (pemphigus vulgaris, pemphigus foliaceus, and other subtypes of pemphigus). The variants of pemphigus are determined according to the level of intraepidermal split formation. There are 5 main variants of pemphigus: pemphigus vulgaris, pemphigus foliaceus, pemphigus erythematosus, drug-induced pemphigus, and paraneoplastic pemphigus. This review focuses only on pemphigus vulgaris.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21605802     DOI: 10.1016/j.det.2011.03.004

Source DB:  PubMed          Journal:  Dermatol Clin        ISSN: 0733-8635            Impact factor:   3.478


  6 in total

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4.  Advanced Diagnostic Techniques in Autoimmune Bullous Diseases.

Authors:  Anuradha Jindal; Raghavendra Rao; Balbir S Bhogal
Journal:  Indian J Dermatol       Date:  2017 May-Jun       Impact factor: 1.494

5.  Esophageal Nikolsky's Sign: A Rare Finding in a Patient with Bullous Pemphigoid.

Authors:  Sara Ghoneim; Aun Shah; Amy Calderon
Journal:  Case Rep Gastroenterol       Date:  2019-10-30

6.  Up-regulation of ST18 in pemphigus vulgaris drives a self-amplifying p53-dependent pathomechanism resulting in decreased desmoglein 3 expression.

Authors:  Sari Assaf; Dan Vodo; Kiril Malovitski; Janan Mohamad; Shir Bergson; Yarden Feller; Liron Malki; Ofer Sarig; Eli Sprecher
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  6 in total

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