Literature DB >> 20164844

Acral peeling skin syndrome with TGM5 gene mutations may resemble epidermolysis bullosa simplex in young individuals.

Dimitra Kiritsi, Ioana Cosgarea, Claus-Werner Franzke, Hauke Schumann, Vinzenz Oji, Jürgen Kohlhase, Leena Bruckner-Tuderman, Cristina Has.   

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Year:  2010        PMID： 20164844     DOI： 10.1038/jid.2010.23

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN： 0022-202X            Impact factor:   8.551


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  4 in total

1.  [Epidermolysis bullosa : Diagnosis and therapy].

Authors:  C Has; L Bruckner-Tuderman
Journal:  Hautarzt       Date:  2011-02       Impact factor: 0.751

2.  [The many facets of inherited skin fragility].

Authors:  C Has; D Kiritsi
Journal:  Hautarzt       Date:  2014-06       Impact factor: 0.751

3.  Acral peeling skin syndrome resembling epidermolysis bullosa simplex in a 10-month-old boy.

Authors:  S Kavaklieva; I Yordanova; L Bruckner-Tuderman; C Has
Journal:  Case Rep Dermatol       Date:  2013-08-07

Review 4.  Inheritance of Monogenic Hereditary Skin Disease and Related Canine Breeds.

Authors:  Pablo Jesús Marín-García; Lola Llobat
Journal:  Vet Sci       Date:  2022-08-15
  4 in total

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